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Quality Assurance Associate

BZAM Management Inc. Pitt Meadows, BC Full-time, Permanent
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The Quality Assurance Associate will report to the Quality Assurance Manager (QAP) or Alternate QAP in lieu and designated management as required. The Quality Assurance Associate is responsible for supporting the Quality Assurance initiatives within the department to ensure that cannabis products produced meet the organization’s objectives for quality, safety, regulatory and customer expectations in accordance with the Cannabis Act and Regulations in accordance with Health Canada guidelines.

ABOUT US:

BZAM is as awesome as it sounds! We are an integrated cannabis company whose mission and brand stand for quality and integrity. Our commitment to excellence, service and employee satisfaction is demonstrated in our agile and strategic approach to market entry and investment in our people. As an emerging company in a rapid growth industry, BZAM’s innovative and accomplished leadership team is the cornerstone of our business and portfolio development.

YOUR CONTRIBUTION:

Ø Support the Quality Assurance Department in implementing SOPs & Quality Management Programs and projects to ensure GPP compliance under the Cannabis Act/Regulations; work cross-departmentally to implement SOPs (i.e. Operations, Regulatory, Security);

Ø Assist in implementation of training programs around SOPs pertaining to GPP and Record Keeping Compliance; collaborate training programs with Human Resources and assess training gaps continuously;

Ø Support the QA Department’s quality programs/systems for cannabis storage;

Ø Assist in the implementation of programs around GPP & Record Keeping Methods for sanitation of premises, equipment, cleanliness, hygienic behaviour of personnel, and facility maintenance;

Ø Collaborate with Regulatory and Security Departments to develop and perform internal audits regularly to determine quality assurance compliance according to Cannabis Regulations;

Ø Maintain current knowledge of best practices for the provisions of the Cannabis Act and Cannabis Regulations that apply to the license holder; and

Ø Other duties as assigned.

WHAT YOU BRING:

Ø BSc. in Chemistry, Biology, Pharmacology or Food Science, obtained or recognized by a Canadian University;

Ø 3+ years’ professional experience in Quality Assurance/Control in a production environment;

Ø Preferred knowledge of plant chemistry, extraction and formulation systems, and chromatographic techniques;

Ø Recent criminal record check completed (required prior to hiring);

Ø Solid ERP, MS Office Suite, Adobe Pro, G-Suite and additional technical proficiency; and

Ø Valid security clearance (ACMPR or Cannabis Regulations).

You Are FOCUSED, DETAIL ORIENTED, AND METHODICAL. Nothing gets by you and you are a master at time management.

You are a CLEAR COMMUNICATOR capable of speaking and writing professionally, clearly and concisely.

You are a RESEARCH GURU, proficient in researching and retaining complicated compliance knowledge.

You are ORGANIZED and strongly skilled in the area of project management.

YOUR EXPERIENCE:

Ø Proven knowledge and demonstrable experience in the stated responsibilities of the position (i.e. Food, Pharma, NHP);

Ø Experience in creating and supporting process enhancement initiatives to maintain an environment of continuous learning and improvement;

Ø Preferred experience with cGMP, GAP, GLP, HACCP, ISO and FDA;

Ø Preferred experience with design inspection methods, fabrication and production of medical cannabis; and

Ø Experience working with technical reports, hazard critical control analysis, and inspecting production resources and materials.

WHAT WE OFFER:

Ø Competitive Compensation and Benefits Package

Ø Rapid growth and advancement potential

Ø Learning and development opportunities

Ø Dynamic and innovative environment

Ø Exceptional culture

BZAM is an Equal Employment Opportunity employer that values the strength of diversity within the workplace. All qualified applicants, regardless of race, colour, religion, gender, sexual orientation, marital status, gender identity or expression, nationality, age, disability or veteran status, or any other characteristic protected by applicable law, are strongly encouraged to apply.

Job Types: Full-time, Permanent

Benefits:

  • Dental care
  • Extended health care
  • RRSP match
  • Vision care

COVID-19 considerations:
BZAM Cannabis is committed to following all provincial and federal public health authority guidance pertaining to COVID-19

Education:

  • Bachelor's Degree (preferred)

Experience:

  • Quality assurance or Quality Control: 3 years (preferred)
  • cGMP, GAP, GLP, HACCP, ISO and FDA: 2 years (preferred)
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As an emerging company in a rapid growth industry, BZAM’s innovative and accomplished leadership team is the cornerstone of our business and portfolio development.</p><p><b>YOUR </b><b>CONTRIBUTION: </b></p><p>Ø Support the Quality Assurance Department in implementing SOPs &amp; Quality Management Programs and projects to ensure GPP compliance under the Cannabis Act/Regulations; work cross-departmentally to implement SOPs (i.e. Operations, Regulatory, Security);</p><p>Ø Assist in implementation of training programs around SOPs pertaining to GPP and Record Keeping Compliance; collaborate training programs with Human Resources and assess training gaps continuously;</p><p>Ø Support the QA Department’s quality programs/systems for cannabis storage;</p><p>Ø Assist in the implementation of programs around GPP &amp; Record Keeping Methods for sanitation of premises, equipment, cleanliness, hygienic behaviour of personnel, and facility maintenance;</p><p>Ø Collaborate with Regulatory and Security Departments to develop and perform internal audits regularly to determine quality assurance compliance according to Cannabis Regulations;</p><p>Ø Maintain current knowledge of best practices for the provisions of the Cannabis Act and Cannabis Regulations that apply to the license holder; and</p><p>Ø Other duties as assigned.</p><p><b>WHAT YOU BRING: </b></p><p>Ø BSc. in Chemistry, Biology, Pharmacology or Food Science, obtained or recognized by a Canadian University;</p><p>Ø 3+ years’ professional experience in Quality Assurance/Control in a production environment;</p><p>Ø Preferred knowledge of plant chemistry, extraction and formulation systems, and chromatographic techniques;</p><p>Ø Recent criminal record check completed (required prior to hiring);</p><p>Ø Solid ERP, MS Office Suite, Adobe Pro, G-Suite and additional technical proficiency; and</p><p>Ø Valid security clearance (ACMPR or Cannabis Regulations).</p><p>You Are FOCUSED, DETAIL ORIENTED, AND METHODICAL. Nothing gets by you and you are a master at time management.</p><p>You are a CLEAR COMMUNICATOR capable of speaking and writing professionally, clearly and concisely.</p><p>You are a RESEARCH GURU, proficient in researching and retaining complicated compliance knowledge.</p><p>You are ORGANIZED and strongly skilled in the area of project management.</p><p><b>YOUR EXPERIENCE: </b></p><p>Ø Proven knowledge and demonstrable experience in the stated responsibilities of the position (i.e. Food, Pharma, NHP);</p><p>Ø Experience in creating and supporting process enhancement initiatives to maintain an environment of continuous learning and improvement;</p><p>Ø Preferred experience with cGMP, GAP, GLP, HACCP, ISO and FDA;</p><p>Ø Preferred experience with design inspection methods, fabrication and production of medical cannabis; and</p><p>Ø Experience working with technical reports, hazard critical control analysis, and inspecting production resources and materials.</p><p><b>WHAT WE OFFER: </b></p><p>Ø Competitive Compensation and Benefits Package</p><p>Ø Rapid growth and advancement potential</p><p>Ø Learning and development opportunities</p><p>Ø Dynamic and innovative environment</p><p>Ø Exceptional culture</p><p><b><i>BZAM is an Equal Employment Opportunity employer that values the strength of diversity within the workplace. All qualified applicants, regardless of race, colour, religion, gender, sexual orientation, marital status, gender identity or expression, nationality, age, disability or veteran status, or any other characteristic protected by applicable law, are strongly encouraged to apply.</i></b></p><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Dental care</li><li>Extended health care</li><li>RRSP match</li><li>Vision care</li></ul><p>COVID-19 considerations:<br />BZAM Cannabis is committed to following all provincial and federal public health authority guidance pertaining to COVID-19</p><p>Education:</p><ul><li>Bachelor's Degree (preferred)</li></ul><p>Experience:</p><ul><li>Quality assurance or Quality Control: 3 years (preferred)</li><li>cGMP, GAP, GLP, HACCP, ISO and FDA: 2 years (preferred)</li></ul></div>","company":{"companyType":"Private/Established","name":"BZAM Management Inc.","logoUrl":"/logos/bzam-cannabis-b38c86b85c95534fc19e12da77b862d5.jpeg"},"location":{"country":"Canada","address":"Pitt Meadows, BC","city":"Pitt Meadows","stateProvince":"BC"},"frontendLink":"/job-posting/bzam-management-inc/quality-assurance-associate/06f2c6939aede892381936d3bd87e59a","title":"Quality Assurance Associate","hash":"06f2c6939aede892381936d3bd87e59a","postingUrl":"https://ca.indeed.com/job/quality-assurance-associate-042b15d9167d1bf3"},{"postedOn":"3 days ago","description":"<div><div><p>Aqualitas Inc. is a licensed medical cannabis producer, with our corporate Head Office located in Bedford, Nova Scotia, and our Production Facility located on the South Shore of Nova Scotia in the Region of Queens Municipality. We are committed to quality, sustainability and balance; in our products, our operations and our people.</p><p></p><p><b><br />QUALITY ASSURANCE TECHNICIAN- ONE YEAR TERM</b></p><p></p><p><br />We are currently seeking a skilled QA Technician at our production facility located in <b><i>Brooklyn, Queens County, NS</i></b>. Reporting to the QA Manager, you will actively contribute to and support the day-to-day efforts of the QA/QC Team across all departments at the facility.</p><p></p><p><b><br />Responsibilities include, but are not limited to</b><b>:</b></p><p></p><ul><li><br />Maintaining operations by strictly adhering at all times to company, industry and regulatory Policies, Standard Operating Procedures (SOPs), Work Instructions (WIs), Good Production Practices (GPP), Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and reporting any required changes.</li><li>Maintaining databases by entering new analytical results and QC testing data</li><li>Creating Quality Dashboard and Quality Scorecard for Executive Team review when needed</li><li>Collecting, entering and analyzing data from, as well as inspecting and monitoring as required for, various departments (Packaging, Sanitation, Aquaponics, Cultivation), including:<ul><li>Packaging re-work data</li><li>Finished product inspection</li><li>Trim Room monitoring</li><li>Drying sample collection and monitoring</li><li>Water analysis</li><li>AQL In-process Inspection</li><li>Excise stamp and shipping inspection</li></ul></li><li>Reviewing data for deficiencies and working towards continuous methods to improve data management</li><li>Resolving deficiencies by following SOPs and consulting with QA Manager/QAP regarding incomplete documentation</li><li>Securing information by completing database backups in consultation with IT Technician</li><li>Providing appropriate documents to Post-Production team when needed</li><li>Additional QA tasks as required, including:<ul><li>Packaging Room QA backup</li><li>Training staff on activities and deviations noted in the process</li><li>Conducting line clearances</li><li>Conducting swabbing on rooms and equipment</li></ul></li><li>Maintaining strict confidentiality at all times to protect operations and ensure customer confidence</li><li>Finished product Inspection</li><li>Documents Provided to Post production Team</li><li>Excise Stamps inspection / Shipping Inspection</li><li>Trim room monitoring</li><li>Site audit activities</li><li>Status Labelling</li><li>Drying Sample collection and Monitoring</li><li>Cover other QA shift when required</li><li>Other duties as may be assigned from time to time</li></ul><p></p><p><b><br />Qualifications</b><b>:</b></p><ul><li>Bachelor of Science in Chemistry, Biology or Environmental Science or related manufacturing experience</li><li>Understanding sound quality assurance principles, statistical process control, sanitation</li><li>Familiarity with pH meter and moisture analyzers, micro swabbing and calibration of equipment</li><li>Good understanding of GPP/EU-GMP, HACCP</li><li>Experience with GPP/GMP Standards</li></ul><p></p><p><b><br />Skills</b><b>:</b></p><ul><li>Accurate and efficient keyboarding and data entry skills</li><li>Advanced knowledge of Excel software</li><li>Keen recordkeeping, editing and documentation abilities</li><li>Superior time management and organizational abilities to establish entry and daily task priorities</li><li>Comfort level working in groups or individually</li><li>Comfort level of working with groups to collaborate and communicate</li><li>Self directed to know the needed schedule day to day</li></ul><p></p><p><b><br />Other details</b><b>:</b></p><p><i>Location</i>: Brooklyn, NS (Required); occasional travel to Bedford/HRM area may be possible</p><p><i>Compensation</i>: To be determined based on skills and experience</p><p><i>Status and Hours</i>: One year Term, Full-Time (40 hrs/week)</p><p></p><p><b><i><br />Successful applicants must provide satisfactory background and reference checks.</i></b></p><p></p><p><br />Aqualitas welcomes and encourages diversity. Should you require an accommodation in any aspect of our selection process, please let us know.</p><p></p><p><br />We appreciate the interest of all candidates; however, we will only be contacting those that best fit our requirements. Resumes will be kept for consideration for six months.</p></div></div>","company":{"companyType":"Private/Growth","name":"Aqualitas Inc.","logoUrl":"/logos/aqualitas-3e7851baa3715671eadbf19c677e9a3a.jpeg"},"location":{"country":"Canada","address":"Brooklyn, NS","city":"Brooklyn","stateProvince":"NS"},"frontendLink":"/job-posting/aqualitas-inc/quality-assurance-technician/abf728e1323c0d61d2f2e4dad8edfb4f","title":"Quality Assurance Technician","hash":"abf728e1323c0d61d2f2e4dad8edfb4f","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-2db6895971d1c2e8"},{"employmentType":"Full-time, Permanent","postedOn":"3 days ago","description":"<div><p><b>Position: </b> Quality Assurance Technician<br /><b>Reporting To: </b> QA Manager<br /><b>Location: </b> Calgary, AB<br /><b>Type: </b> Full Time, Permanent</p><p><b>The Position</b></p><p>OGEN is looking for a highly motivated and detail-oriented individual to join our growing team! The Quality Assurance Technician is an entry-level position that is responsible for the daily administrative duties of the department. The ideal candidate is organized, communicative, proficient with computer applications, and adaptable. This high-volume position requires the ability to work under pressure in a fast-paced environment with competing deadlines and priorities.</p><p><b>About OGEN LTD.</b></p><p>OGEN LTD. is a licensed producer located in Calgary, Alberta. We cultivate small-batch, craft cannabis to deliver a high-end, dried flower product of exceptional quality. We work as a team and are proud to grow in a world-class indoor hydroponic facility.</p><p><b>Position Duties and Responsibilities</b></p><p>Reporting to the Quality Assurance Manager, the selected candidate’s duties and responsibilities will include the following:</p><p>· Assist in filing, records review, distribution, archival, logbooks, and all required follow-up</p><p>· Perform label control process: preparation, counting, inventory, issuance, and destruction</p><p>· Assist with Production Work Order (PWO) documents: issuance and retrieval</p><p>· Review of Quality Control (QC) raw data results, and reports</p><p>· Coordination of sample shipments to laboratories</p><p>· Support the inspection of incoming materials and assist with material release</p><p>· Identify non-conformities and deviations and assist with investigations, as required</p><p>· Understand and follow SOPs and procedures to GMP/GPP standards</p><p>· Assist the QA Associate, QA Manager, and QA Director, as required</p><p><b>Minimum Requirements</b></p><p>· Successfully pass a criminal record check and other security-related requirements</p><p>· Must be legally entitled to work in Canada</p><p>· Must be 18 years of age or older</p><p>· Minimum of 1 year of experience working in Quality Control</p><p>· Completion of High School Diploma or equivalent</p><p>· Some post-secondary education in a related field</p><p>· Proficient in Microsoft Office suites and adept at learning new software programs</p><p><b>Soft Skills</b></p><p>· Must have good interpersonal skills to maintain effective work relationships</p><p>· Excellent written and verbal communication skills</p><p>· Highly organized and strong attention to detail skills</p><p>· Possess a high level of problem-solving abilities and remain calm in all situations</p><p><b>Position Preferences</b></p><p>· Experience in a cannabis, liquor, tobacco, pharmaceutical or other highly regulated industry</p><p>· Understanding of a Document Control System within a manufacturing environment</p><p>· Familiarity with GPP and/or GMP</p><p><b>Working Conditions and Physical Requirements </b></p><p>· Willingness to perform repetitive tasks</p><p>· Ability to work under high pressure in a fast-paced environment managing multiple priorities</p><p><b>How to Apply</b></p><p>If this position sounds like the right fit and opportunity for you, please submit a cover letter and resume for consideration. Your cover letter should address the following qualification questions:</p><ul><li>Would you successfully pass a criminal background check and security-related requirements?</li><li>What previous experience and skills would make you the ideal candidate for this role?</li><li>Why do you want to work for OGEN?</li><li>How did you hear about this position?</li></ul><p><b>Stay Connected to Us</b></p><p>Follow us on LinkedIn, Facebook, and Instagram for the latest news and job postings</p><p><b>Our Values</b></p><p><b>STREET: </b>we honour the pioneers before us. Without them, the landrace strains would be extinct and new hybrids would not exist. We follow in their footsteps, to maintain the art of cultivation.</p><p><b>SCIENCE: </b>we are forward thinkers, inspired by science, technology and data. We continuously improve our processes by hypothesizing, gathering data, and applying our knowledge. It helps us cultivate consistently and safely to meet the strict cannabis regulations.</p><p><b>QUALITY: </b>we are connoisseurs, not mass producers. We select the best genetics and we pheno-hunt. We take the time to hang-dry, hand-trim and slow cure our cannabis. Our expectations are high because we demand top quality for our customers and ourselves.</p><p><b>HUMILITY: </b>with every new challenge we find a better way, we push the boundaries and we don’t give up.</p><p><b>COMMUNITY: </b>we are proud to be local and we share the entrepreneurial spirit of Alberta. We believe in the craft movement, an appreciation of how things are carefully made.</p><p>Reference ID: QAT05122021WHW</p><p>Application deadline: 2021-06-16</p><p>Expected start date: 2021-05-31</p><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Extended health care</li><li>On-site parking</li><li>Paid time off</li></ul><p>Schedule:</p><ul><li>Day shift</li><li>Monday to Friday</li><li>Overtime</li></ul><p>Application question(s):</p><ul><li>What previous experience and skills would make you the ideal candidate for this role?</li><li>Would you successfully pass a criminal background check and security-related requirements?</li></ul><p>Education:</p><ul><li>Secondary School (required)</li></ul><p>Experience:</p><ul><li>Administrative experience: 1 year (required)</li><li>Manufacturing: 1 year (preferred)</li><li>Microsoft Office: 2 years (preferred)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Public/Growth","name":"OGEN LTD.","logoUrl":"/logos/ogen-ltd-edbcc55fff7e49bc7c001f74ae0d7ceb.jpeg"},"location":{"country":"Canada","address":"Calgary, AB","city":"Calgary","stateProvince":"AB"},"frontendLink":"/job-posting/ogen-ltd/quality-assurance-technician/35a611487da46f8c8924ca06b02c2dc8","title":"Quality Assurance Technician","hash":"35a611487da46f8c8924ca06b02c2dc8","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-4da557ecf5b9c140"},{"employmentType":"Full-time","postedOn":"11 hours ago","description":"<div><p><b>COMPANY</b></p><p>We are setting the industry standard to influence and inspire through our innovative methods. We merge together cannabis culture with cutting-edge technology to deliver the best possible customer and employee experience(s).</p><p>The company operates a fully integrated cannabis business with a footprint that covers the entire breadth of the state of California; the world's largest cannabis market. We control our supply chain from cultivation to retail, which enables us to deliver clean and tested cannabis products at unmatched prices.</p><p>Our mission is to provide the one-stop-shop cannabis experience by offering exceptional customer experience service and diversified products. We strive to build long-term customer loyalty.</p><p><b>POSITION</b></p><p>We're seeking energetic QC Technicians to assist the Operations Management team with daily functions that will support many facets of the company. The ideal candidate will be punctual, detail-oriented, trustworthy, and willing to flex into a new role at any given moment. This is an entry-level position, in which the QC Technicians are responsible for the control of product quality, quantity, and safety while following BCC, cGMP, CDFA, CDPH, FDA, and ISO guidelines. One must have the ability to monitor acceptable quality limits (AQL) set by the company’s Quality Department and to enforce prompt and necessary corrective actions<b>. Cannabis Industry experience is a plus!</b></p><p>SHIFT - 6:00 am-2:30 pm)</p><p><b>WHO SHOULD APPLY</b></p><ul><li>To belong to a community of relentlessly dedicated individuals driven by a passion to be a best in class cannabis brand</li></ul><ul><li>To do exceptionally meaningful work that helps to improve other's quality of life.</li></ul><ul><li>You have an entrepreneurial spirit; guided by an authentic understanding of cannabis and cannabis culture; and committed to social justice.</li></ul><ul><li>The opportunity to work for a growing company that is positioned to become a globally recognized brand in the cannabis industry</li></ul><ul><li>Significant opportunity for growth, experience, and learning in a startup company</li></ul><p><b>KEY ATTRIBUTES FOR SUCCESS</b></p><ul><li>A resilient and entrepreneurial spirit with a growth mindset</li></ul><ul><li>A true team player willing to roll up your sleeves and do what needs to be done to succeed</li></ul><ul><li>Ability to work autonomously and take ownership</li></ul><ul><li>Able to create, maintain and build professional relationships and rapport</li></ul><ul><li>Have a strong desire to grow professionally and personally</li></ul><ul><li>Have a sound knowledge of market trends</li></ul><ul><li>Flexibility - this role will be ever-changing</li></ul><p><b>RESPONSIBILITIES</b><br />*</p><ul><li>Perform Microbiological swabbing of equipment and environment and document results.</li></ul><ul><li>Perform periodic weight monitoring and quality inspections and alert production of any non-compliance for prompt adjustment.</li></ul><ul><li>Promptly reports issues to Quality Control Manager, which includes any unfavorable results if corrective actions do not resolve issues.</li></ul><ul><li>Ensure batch records are correctly filled out and logbooks are properly maintained.</li></ul><p><b>QUALIFICATIONS</b></p><ul><li>Comfortable in a fast-paced start-up atmosphere environment and able to adapt to changing priorities.</li><li>Must show good attention to detail and possess good people skills and be able to multitask and work under pressure and good organization skills.</li></ul><ul><li>Ability to wear the required PPE and practice safe work practices.</li></ul><ul><li>Possess a willingness to learn new skills and traits, also express an optimistic outlook and be ready for growth.</li></ul><ul><li>Specific vision abilities required include close vision, distance vision, peripheral vision, and the ability to adjust focus.</li></ul><ul><li>Cannot be color blind.</li></ul><ul><li>Must have basic computer proficiency and competence in Microsoft Word and Excel.</li></ul><ul><li>Comfortable with monotonous working assignments and willing to cross-training in different departments.</li></ul><ul><li>Ability to work independently and within a team and willing to take direction as needed.</li></ul><ul><li>Must have good Math knowledge, including the use of decimal conversions.</li></ul><ul><li>Comfortable with attending weekly or monthly meetings and training classes.</li></ul><ul><li>Well-developed interpersonal skills and professional demeanor, with an ability to interact with employees and others at any level within the organization.</li></ul><ul><li>Ability to handle sensitive and confidential information with extreme professionalism.</li></ul><p><b>EDUCATION</b></p><ul><li>Minimum of a High School diploma; preferred Associate’s degree and previous experience in a quality control environment, preferably in a cGMP/FDA/ISO setting (preferred, but is not required).</li></ul><p><b>PHYSICAL REQUIREMENTS</b></p><p>The physical demands described here are representative of those that must be met by an associate to successfully perform the essential functions of this job.</p><p>Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><ul><li>Prolonged periods of sitting at a desk and working on a computer.</li></ul><ul><li>Must be able to lift 50 pounds at times.</li></ul><ul><li>Must be able to access and navigate each department at the organization's facilities.</li></ul><ul><li>Be able to stand, and sit for prolonged periods of time, bend, kneel, squat, and twist</li></ul><p>Due to Covid-19, we are doing everything we can to keep our team and customers safe. This means individual offices or widely spaced workstations. We also provide extra masks, shields, hand sanitizer, and gloves as needed. We are an essential business and we require our team to work in the office.</p><p><i>We provide equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</i></p><p><i>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.</i><br />*</p><p>Job Type: Full-time</p><p>Pay: $15.00 - $17.00 per hour</p><p>Benefits:</p><ul><li>401(k)</li><li>Dental insurance</li><li>Employee discount</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Ability to Commute/Relocate:</p><ul><li>Los Angeles, CA 90012 (Required)</li></ul><p>Application Question(s):</p><ul><li>Are you 21 years of age or older? (Cannabis regulations require is to ask)</li></ul><p>Education:</p><ul><li>High school or equivalent (Preferred)</li></ul><p>Experience:</p><ul><li>Quality control: 3 years (Required)</li><li>Microsoft Word: 2 years (Preferred)</li><li>Microsoft Excel: 2 years (Preferred)</li><li>Cannabis Industry: 1 year (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"STIIIZY","logoUrl":"/logos/stiiizy-efa24894850a97a1c268f8e7502aca7c.png"},"location":{"country":"United States","address":"Los Angeles, CA 90012","city":"Los Angeles","stateProvince":"CA"},"frontendLink":"/job-posting/stiiizy/quality-control-technician-6-00-am-2-30-pm/f461b0a13536d600bfbeea7df9b77434","title":"Quality Control Technician (6:00 am-2:30 pm)","hash":"f461b0a13536d600bfbeea7df9b77434","postingUrl":"https://www.indeed.com/job/quality-control-technician-600-am-230-pm-44b58db72ff6b0d7"},{"employmentType":"Full-time","postedOn":"11 hours ago","description":"<div><p><b>COMPANY</b></p><p>We are setting the industry standard to influence and inspire through our innovative methods. We merge together cannabis culture with cutting-edge technology to deliver the best possible customer and employee experience(s).</p><p>The company operates a fully integrated cannabis business with a footprint that covers the entire breadth of the state of California; the world's largest cannabis market. We control our supply chain from cultivation to retail, which enables us to deliver clean and tested cannabis products at unmatched prices.</p><p>Our mission is to provide the one-stop-shop cannabis experience by offering exceptional customer experience service and diversified products. We strive to build long-term customer loyalty.</p><p><b>POSITION</b></p><p>We're seeking energetic QC Technicians to assist the Operations Management team with daily functions that will support many facets of the company. The ideal candidate will be punctual, detail-oriented, trustworthy, and willing to flex into a new role at any given moment. This is an entry-level position, in which the QC Technicians are responsible for the control of product quality, quantity, and safety while following BCC, cGMP, CDFA, CDPH, FDA, and ISO guidelines. One must have the ability to monitor acceptable quality limits (AQL) set by the company’s Quality Department and to enforce prompt and necessary corrective actions<b>. Cannabis Industry experience is a plus!</b></p><p>SHIFT - 3:00 pm-12:00 am</p><p><b>WHO SHOULD APPLY</b></p><ul><li>To belong to a community of relentlessly dedicated individuals driven by a passion to be a best in class cannabis brand</li></ul><ul><li>To do exceptionally meaningful work that helps to improve other's quality of life.</li></ul><ul><li>You have an entrepreneurial spirit; guided by an authentic understanding of cannabis and cannabis culture; and committed to social justice.</li></ul><ul><li>The opportunity to work for a growing company that is positioned to become a globally recognized brand in the cannabis industry</li></ul><ul><li>Significant opportunity for growth, experience, and learning in a startup company</li></ul><p><b>KEY ATTRIBUTES FOR SUCCESS</b></p><ul><li>A resilient and entrepreneurial spirit with a growth mindset</li></ul><ul><li>A true team player willing to roll up your sleeves and do what needs to be done to succeed</li></ul><ul><li>Ability to work autonomously and take ownership</li></ul><ul><li>Able to create, maintain and build professional relationships and rapport</li></ul><ul><li>Have a strong desire to grow professionally and personally</li></ul><ul><li>Have a sound knowledge of market trends</li></ul><ul><li>Flexibility - this role will be ever-changing</li></ul><p><b>RESPONSIBILITIES</b><br />*</p><ul><li>Perform Microbiological swabbing of equipment and environment and document results.</li></ul><ul><li>Perform periodic weight monitoring and quality inspections and alert production of any non-compliance for prompt adjustment.</li></ul><ul><li>Promptly reports issues to Quality Control Manager, which includes any unfavorable results if corrective actions do not resolve issues.</li></ul><ul><li>Ensure batch records are correctly filled out and logbooks are properly maintained.</li></ul><p><b>QUALIFICATIONS</b></p><ul><li>Comfortable in a fast-paced start-up atmosphere environment and able to adapt to changing priorities.</li><li>Must show good attention to detail and possess good people skills and be able to multitask and work under pressure and good organization skills.</li></ul><ul><li>Ability to wear the required PPE and practice safe work practices.</li></ul><ul><li>Possess a willingness to learn new skills and traits, also express an optimistic outlook and be ready for growth.</li></ul><ul><li>Specific vision abilities required include close vision, distance vision, peripheral vision, and the ability to adjust focus.</li></ul><ul><li>Cannot be color blind.</li></ul><ul><li>Must have basic computer proficiency and competence in Microsoft Word and Excel.</li></ul><ul><li>Comfortable with monotonous working assignments and willing to cross-training in different departments.</li></ul><ul><li>Ability to work independently and within a team and willing to take direction as needed.</li></ul><ul><li>Must have good Math knowledge, including the use of decimal conversions.</li></ul><ul><li>Comfortable with attending weekly or monthly meetings and training classes.</li></ul><ul><li>Well-developed interpersonal skills and professional demeanor, with an ability to interact with employees and others at any level within the organization.</li></ul><ul><li>Ability to handle sensitive and confidential information with extreme professionalism.</li></ul><p><b>EDUCATION</b></p><ul><li>Minimum of a High School diploma; preferred Associate’s degree and previous experience in a quality control environment, preferably in a cGMP/FDA/ISO setting (preferred, but is not required).</li></ul><p><b>PHYSICAL REQUIREMENTS</b></p><p>The physical demands described here are representative of those that must be met by an associate to successfully perform the essential functions of this job.</p><p>Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><ul><li>Prolonged periods of sitting at a desk and working on a computer.</li></ul><ul><li>Must be able to lift 50 pounds at times.</li></ul><ul><li>Must be able to access and navigate each department at the organization's facilities.</li></ul><ul><li>Be able to stand, and sit for prolonged periods of time, bend, kneel, squat, and twist</li></ul><p>Due to Covid-19, we are doing everything we can to keep our team and customers safe. This means individual offices or widely spaced workstations. We also provide extra masks, shields, hand sanitizer, and gloves as needed. We are an essential business and we require our team to work in the office.</p><p><i>We provide equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</i></p><p><i>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.</i></p><p>Job Type: Full-time</p><p>Pay: $15.00 - $17.00 per hour</p><p>Benefits:</p><ul><li>401(k)</li><li>Dental insurance</li><li>Employee discount</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Ability to Commute/Relocate:</p><ul><li>Los Angeles, CA 90012 (Required)</li></ul><p>Application Question(s):</p><ul><li>Are you 21 years of age or older? (Cannabis regulations require is to ask)</li></ul><p>Education:</p><ul><li>High school or equivalent (Preferred)</li></ul><p>Experience:</p><ul><li>Quality control: 3 years (Required)</li><li>Microsoft Word: 2 years (Preferred)</li><li>Microsoft Excel: 2 years (Preferred)</li><li>Cannabis Industry: 1 year (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"STIIIZY","logoUrl":"/logos/stiiizy-efa24894850a97a1c268f8e7502aca7c.png"},"location":{"country":"United States","address":"Los Angeles, CA 90012","city":"Los Angeles","stateProvince":"CA"},"frontendLink":"/job-posting/stiiizy/quality-control-technician-3-00-pm-12-00-am/0c09b42b8a8a2b975cc695ef3930cad4","title":"Quality Control Technician (3:00 pm-12:00 am)","hash":"0c09b42b8a8a2b975cc695ef3930cad4","postingUrl":"https://www.indeed.com/job/quality-control-technician-300-pm-1200-am-c959c7ea3fc8692f"},{"employmentType":"Full-time","postedOn":"3 days ago","description":"<div><p><b>Job Description</b></p><p><b>Quality Assurance Technician</b></p><p>Location: Jacksonville, FL</p><p>As a Quality Assurance (QA) Technician, you will be responsible for assisting with quality-related activities including start-up verification, in-process verification &amp; checks, BMR and documentation reviews, sampling, and inspection of finished products. Products include cannabis flower, cannabis oil, infused products (concentrates, capsules, lotions, tinctures, vapes, etc.) and food products (chocolate, gummies, lozenges, etc.). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.</p><p><b>Job Summary and Responsibilities</b>:</p><p>- Performs finished product sampling and inspection</p><p>- Performs equipment and product line clearances before production runs</p><p>- Performs in-process verification to ensure product weights, correct labeling &amp; packaging</p><p>- Performs verification on finished products</p><p>- Inspects retain samples and customer return samples, as deemed necessary</p><p>- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product</p><p>- Inspects packaged orders to ensure correct content and quantities, as deemed necessary</p><p>- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures</p><p>- Monitors compliance to established Good Manufacturing Practice (GMP) and Safe Quality Foods guidance</p><p>- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines</p><p>- May require travel to other states or facilities to assist with inspections or quality issues</p><p><b>Required Experience, Education and Skills: </b></p><p>- Bachelors Degree, 1-3 years’ experience or Associate Degree, 5+ years’ experience</p><p>- Prior experience in highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, SQF experience</p><p>- Prior experience in Quality Assurance or Quality Control function</p><p>- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA</p><p>- Ability to follow written procedures and monitor others for adherence to written procedures</p><p>- Ability to create or update written procedures with site operations personnel</p><p>- Strong written and verbal communication skills</p><p>- Detail-oriented</p><p>- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</p><p>- Must be flexible and able to work long hours and weekends as required</p><p>- Able to adapt in a quick and positive manner</p><p>- Able to work in a fast-paced environment and handle multiple tasks and requests</p><p><b>Additional Requirements</b>:</p><p>- Must be 21 years of age or older</p><p>- Must comply with all legal and company regulations for working in the industry</p><p>- Ability to stand throughout extended periods, must be capable of squatting, standing, kneeling, bending, or walking throughout the workday</p><p>- Excellent communication skills and leadership both verbally and through written media.</p><p>- Strong decision-making, analytical and organizational skills</p><p>- Thorough understanding of state and local medical marijuana laws and how they apply to the operations</p><p><b>Physical Demands: </b></p><p>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</p><p>While performing the duties of this Job, the employee is regularly required to stand for extended periods every day. The employee must regularly lift and /or move up to 25 pounds, frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Able to work 6 days a week and evening shifts if required.</p><p><b>Work Environment: </b></p><p>While performing the duties of this job, the employee will be standing indoors and frequently exposed to laboratory conditions. The employee is frequently exposed to fumes or airborne particles; toxic or caustic chemicals; and varying temperatures. The noise level in the work environment is usually loud.</p><p>Job Type: Full-time</p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Employee discount</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>COVID-19 considerations:<br />All employees are required to wear a mask</p><p>Experience:</p><ul><li>Quality control: 1 year (Required)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Established","name":"VidaCann","logoUrl":"/logos/vidacann-d27624162f7a910e07f93f882426ed6c.jpeg"},"location":{"country":"United States","address":"Jacksonville, FL 32216","city":"Jacksonville","stateProvince":"FL"},"frontendLink":"/job-posting/vidacann/quality-assurance-technician/cdcc1f2170e4962f05ed1f46f739648a","title":"Quality Assurance Technician","hash":"cdcc1f2170e4962f05ed1f46f739648a","postingUrl":"https://www.indeed.com/job/quality-assurance-technician-87c73aa8e0a8b69d"},{"postedOn":"1 day ago","description":"<div><div><div><p><b>Title:</b> Quality Specialist Department: Quality</p><p><b>Reporting To</b>: Quality Manager</p><p><b>Status:</b> Regular Full-Time, Non-Exempt</p><p><b>Direct Reports:</b> None</p><p><b>Location:</b> CSA LA Lab</p></div><br /><div></div><p><b>Job Summary</b></p><p>The Quality Control Specialist is responsible for executing the Company’s quality control program by using established quality policies and measures to monitor and ensure compliance with BCC regulations, CDFA regulations, and ISO 17025 accreditation. Our Quality department serves as a key check and balance measure in our operation and requires adherence to and modeling of the highest ethical standards.</p><p><b>Essential Duties and Responsibilities</b></p><ul><li>Communicate quality policies and procedures to all levels of the organization – from entry-level to executive.</li></ul><ul><li>Review and release Certificates of Analysis (CoAs) prior to release and ensure all reported information is accurate.</li></ul><ul><li>Assist in managing the proficiency test program and performing ring tests for laboratory assays.</li></ul><ul><li>Assist in verifying comprehensiveness of analytical batches, including test records, batch size, quality control samples, calibration, and similar.</li></ul><ul><li>Assist in investigating non-conformance events and conduct root cause analysis investigations. Generate reports, ensure corrective action is taken, recommend preventive action, and follow-up to confirm timely implementation as necessary.</li></ul><ul><li>Assist with internal and external audits. This may include, but is not limited to: inspecting and verifying compliance test records, compiling data packets, investigating deficiency findings, drafting corrective/preventive actions and following-up, as well as drafting audit reports. Offsite audits may include sampling and other lab facilities.</li></ul><ul><li>Assist with our internal training program to ensure all employees are assigned and have completed required training.</li></ul><ul><li>Provide general laboratory support, such as establishing, reviewing, and updating SOPs, attending meetings, and troubleshooting technical issues.</li></ul><ul><li>Confer with interdepartmental staff on questionable information or test results (anomalies) and assist in correcting the information as necessary.</li></ul><ul><li>Document and conduct investigations in response to customer complaints. Communicate findings to all appropriate internal and external parties.</li></ul><ul><li>Assist with data packet compilation and review of test records, analytical batch requirements, quality control samples, raw data, chromatograms, and similar.</li></ul><ul><li>Troubleshoot and investigate Metrc issues and inquiries from customers.</li></ul><ul><li>Interpret test results and assess compliance.</li></ul><ul><li>Other duties and special projects as assigned.</li></ul><p><b>Knowledge, Skills, and Abilities</b></p><ul><li>Demonstrated proficiency in quality assurance/control in a laboratory or similar environment, including working knowledge of HPLC, GC, ICP, and/or PCR instrumentation.</li></ul><ul><li>Ability to maintain an incredibly high degree of attention to detail and accuracy.</li></ul><ul><li>Strong agility, engagement, and flexibility in an ever-changing environment.</li></ul><ul><li>Diligent commitment to logging, organizing, and analyzing data.</li></ul><ul><li>Ability to work in a dynamic, fast-paced deadline environment while successfully managing multiple tasks.</li></ul><ul><li>Strong knowledge of Microsoft Office, including Excel, PowerPoint, and Word.</li></ul><ul><li>Strong understanding of standard laboratory protocol.</li></ul><ul><li>Excellent communication skills and ability to effectively work, problem solve, and communicate with multiple levels of the organization.</li></ul><p><b>Education and Experience</b></p><ul><li>Required: A bachelor’s degree in a scientific field from a four-year college or university.</li></ul><ul><li>Required: Knowledge of principles, terminology, practices, techniques, and instrumentation commonly used in a laboratory setting.</li></ul><ul><li>Preferred: At least four (4) years of relevant quality operations experience in a regulated industry, such as USDA, FDA, EPA, NELAC, etc.</li></ul><ul><li>Optional: Exposure to the cannabis industry.</li></ul><p><b>Essential Functions</b></p><p>The physical demands described here are representative of those that an employee must meet to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><br /><p></p><p>While performing the duties of this job the employee is frequently required to stand, handle or feel, to speak, and to hear. The employee is occasionally required to walk, sit, reach with hands and arms, bend, kneel, crouch, or crawl. The employee must frequently lift and/or move up to thirty-five (35) pounds. Specific vision abilities required for this job include close (proximity) vision, depth perception, and the ability to adjust focus.</p><p><b>Work Environment</b></p><p>The work environment described here is representative of that which an employee may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><p>The standard analytical laboratory environment is one in which potential health hazards do exist. Administrative, operations, technical, and professional staff are expected to safely operate in accordance with applicable and appropriate health and safety policies and procedures, as prescribed by the applicable CannaSafe manuals and policies and/or federal, state, or local standards.</p><p>Laboratory staff can be expected to work in areas where hazards associated are with, but not limited to, airborne pathogens. Biological materials, hazardous substances, and radioactive material exist and are handled. Appropriate training is provided regarding these hazards and staff are expected to adhere to all health and safety policies at all times, whether they are in writing or verbalized by a supervisor.</p><p> This includes alignment with our Mission, Vision, Values, and Goal, as noted below:</p><p><b>Mission:</b> The pursuit of safe cannabis and hemp for all.</p><p><b>Vision:</b> To be #1 in cannabis and hemp safety.</p><p><b>Core Values:</b></p><ul><li>Integrity: Lead by example and never compromise.</li></ul><ul><li>Leadership: Be empathetic, a true TEAMmate, and always solutions-focused.</li></ul><ul><li>Accountability: Take ownership and stand behind your actions.</li></ul><ul><li>Communication: Listen first and never stop communicating.</li></ul><ul><li>Focus: Stay the course and get it done.</li></ul><ul><li>Winning Attitude: Be positive and persevere no matter what.</li></ul><p><b>Goal:</b> To be an upstanding member of the community and a great place to work.</p></div></div>","company":{"companyType":"Private/Established","name":"CannaSafe","logoUrl":"/logos/cannasafe-0759740914f0eb80b569ecc26e94ac2b.png"},"location":{"country":"United States","address":"Van Nuys, CA 91406","city":"Van Nuys","stateProvince":"CA"},"frontendLink":"/job-posting/cannasafe/quality-specialist/18f3fbe146d11bfa0507b1610bb807fa","title":"Quality Specialist","hash":"18f3fbe146d11bfa0507b1610bb807fa","postingUrl":"https://www.indeed.com/job/quality-specialist-7d93682bfa387b3e"},{"employmentType":"Full-time","postedOn":"4 days ago","description":"<div><p><b>Quality Assurance Technician - DAY ShiftDescriptionJob Title:</b></p><p><b>Quality Assurance Technician Department:</b></p><p><b>Quality AssuranceReports to:</b></p><p><b>QA Supervisor or Team LeadFLSA Status:</b></p><p><b>Regular Full-Time Salary:</b></p><p><b>HourlyLocation:</b></p><p>Quincy (Ben Bostic)Role SummaryThe Quality Assurance Technician is responsible for conducting visual scans on products in effort to assure quality and safety of products intended for consumers.</p><p>QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on.</p><p><b>Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans.Key Duties and Responsibilities:</b></p><p>Conduct visual inspections of cannabis for organic and inorganic adulterants and defects.Document inspection results by completing reports and logs and inputting data into quality database.Keep equipment (i.e.</p><p><b>scales, tools, etc) in good, working order.Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulationsMaintains and ensures that proper PPE is utilized and changed out regularly, or as neededProvide Feedback as neededPerforms other duties as requiredPosition RequirementsSKILLS AND QUALIFICATIONS:</b></p><p><b>High School Diploma or GEDDetail OrientedCoachable and a willingness to learnAbility to work in a fast-paced environmentAbility to focus and avoid distractionsComfortable operating digital scalesBasic computer knowledgeBasic math and reading comprehensionOrganizational skillsADDITIONAL REQUIREMENTS:</b></p><p><b>Florida Driver's License or ability to obtain one.Per state law, must be a minimum of 21 years of age.Must be and remain compliant with any and all legal or company regulations for working in the cannabis industry.Must successfully complete a comprehensive background check.PHYSICAL REQUIREMENTS:</b></p><p>Must be able to push, pull, move, and/or lift a minimum of 40lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistanceMust be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stopping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasksMust be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater)Must have visual acuity with/without job aids to perform activities such as; reading, viewing a computer terminal, visual inspection involving small parts/details.</p><p>Clarity of vision at 20 ft or more in day and night/dark conditionsMust be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc.</p><p><b>(Moderate noise)WORK SCHEDULE:</b></p><p>40+ hours weekly with flexible hours depending on department needs.</p><p>Must be available to work occasional evenings, weekends, and holidaysEqual Opportunity Employer l Trulieve Supports a Drug Free WorkplaceFull-Time/Part-TimeFull-Time ShiftRotating Days and Nights Level 2 Background check requiredPositionQuality Assurance Technician DivisionTrulieve, INC Close DatePost Internal Days0 Number of Openings1 Number Filled0 Exempt/Non-ExemptNon-Exempt Req NumberPRO-21-00080 Open Date3/15/2021 LocationBen Bostic - North EOE StatementWe are an equal employment opportunity employer.</p><p>All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.</p><p>This position is currently accepting applications</p></div>","company":{"website":"trulieve.com","companyType":"Public/Established","name":"Trulieve Cannabis","logoUrl":"/logos/trulieve-1d76a294c42e35e1fad949d6f74742d9.png"},"location":{"country":"United States","address":"Quincy, FL, USA","city":"Quincy","stateProvince":"FL"},"frontendLink":"/job-posting/trulieve-cannabis/quality-assurance-technician-day-shift/ef6325b54472cbbc6d9a53e2af698efc","title":"Quality Assurance Technician - DAY Shift","hash":"ef6325b54472cbbc6d9a53e2af698efc","postingUrl":"https://www.jobilize.com/amp/job/quality-assurance-technician-day-shift-quincy-trulieve-cannabis-united"},{"employmentType":"Full-time","postedOn":"7 days ago","description":"<div><p>QUALITY CONTROL TECHNICIAN Whistler Medical Marijuana Corporation is a wholly owned subsidiary of Aurora Cannabis Enterprises Inc. We are currently recruiting for a Quality Control Technician to join our Facility in Pemberton, British Colombia. The incumbent will report to the Vice President of Quality and will be responsible for the following: MAIN RESPONSIBILITIES: Understand, and follow all department SOPs and related forms to GMP and/or GPP standards, including owning QC procedures. Understanding of Health Canada, USP, EU compliance and requirements. Complete all required documentation using good documentation practices, Develop and align testing specifications for all controlled materials and finished products within Aurora Cannabis standards Maintain functional understanding of HPLC, GC-MS, ICP-MS, spectroscopy, and plant sciences Be responsible for the execution of Quality Control process, including but not limited to: Material Management – sampling, testing, and approval of certificate of analysis of controlled materials. Provide guidance to procurement for suitability of material and vendors Environmental Monitoring – participate in the development and execution of the sampling plan of grow rooms, report state of facility and procedures to minimize risk of contamination Compile specification documents for all tested materials, determine the disposition of the material by assessing compliance of the results to the specification Initiate/Support investigations, to ensure ongoing compliance, to achieve process / quality improvements Be the primary contact and liaison for all communication with outside testing labs Be responsible for sampling and testing of cannabis products both internally and externally to ensure compliance with internal specifications and other needs Consult and/or participate in any sampling process required at the site, with respect to suitability, and compliance Reporting of any potential or actual deviations to Process manager and QA Manager Effective and strong communication with all cross functional teams within the facility Support Quality Assurance as required at the facility Attend and participate in meetings as required Any other suitable duties as assigned by the VP of Quality. DESIRED QUALIFICATIONS: B.Sc. degree or diploma in an applicable discipline of science (chemistry, biochemistry, biology or related) 2+ years experience working in Quality Assurance Knowledge of GMP and regulations for manufacturing and testing pharmaceutical products considered an asset Familiarity with laboratory equipment (e.g. HPLC, GC, and ICP) considered an asset. Proficiency in scientific writing Strong verbal and written communication skills. Strong computer skills. Knowledge with Microsoft excel, word and outlook Ability to thrive in a constantly changing environment. We would like to thank all applicants for their interest but only those selected for an interview will be contacted</p></div>","company":{"website":"cannimed.ca","companyType":"Public/Established","name":"Cannimed By Aurora","logoUrl":"/logos/cannimed-bf99b9c93458faff6d96dc9f331679ce.png"},"location":{"country":"Canada","address":"Corman Park No. 344, SK (+1 other)","city":"Corman Park No. 344","stateProvince":"SK"},"frontendLink":"/job-posting/cannimed-by-aurora/quality-control-technician/96c455f4a306fbceecbccecca2231247","title":"Quality Control Technician","hash":"96c455f4a306fbceecbccecca2231247","postingUrl":"https://ca.trabajo.org/job-51-20210509-e05dbc22671c433de8e2db482e4b29c4"},{"employmentType":"Full-time, Permanent","postedOn":"9 days ago","description":"<div><p><b>About AtlantiCann Medical</b></p><p>AtlantiCann Medical is majority owned by the Mi’kmaq First Nations of Nova Scotia.</p><p>We are proud to be producing quality cannabis in Mi’kma’ki, the ancestral and unceded territory of the Mi’kmaq People. The 8-point star, a symbol very important to the Mi’kmaq community, often presents with 4 colours signifying unity between the four races of people as well as the 4 directions (North, South, East and West), emphasizing balance within oneself and mother earth.</p><p>We are proud to embrace these values and provide Mi’Kmaq product to NS and across the nation.</p><p>We are an equal opportunity employer and adhere to fair employment practices.</p><p>As a Quality Assurance (QA) Technician of a Health Canada Licensed Producer of Cannabis, you will be responsible for quality monitoring, documentation, records handling, and quality control in compliance with Health Canada’s Cannabis Regulations and the European Union GMP Regulations, while taking corrective and preventative measures if necessary.</p><p><b>Roles Responsibilities</b></p><ul><li>Staying current with Health Canada regulations.</li><li>Staying current with European GMP Regulations</li><li>Keeping all records up to date and compliant to regulatory standards in preparation for Health Canada, and EU-GMP audits.</li><li>Working with the Quality Assurance Technician to ensure proper documentation.</li><li>Inventory reporting to Health Canada and Canada Revenue Agency.</li><li>Ensuring all processing activities are completed as per Standard Operating Procedures (SOPs).</li><li>Understanding, implementing, and training on Good Production Practices (GPP).</li><li>In-process quality monitoring and testing.</li><li>Draft, revise, and review SOPs.</li><li>Train staff on SOPs and ensure ongoing compliance.</li><li>Review batch records and lab certificate of analysis and ensuring that all cannabis is approved prior to being made available for sale.</li><li>Sanitation program inspection and verification.</li><li>Record keeping and documentation.</li><li>Responsible for investigating every complaint received in respect of the quality of the cannabis and taking any measures to mitigate risk.</li><li>Development and maintenance of a recall program</li><li>Responsible for approving the preventive control plan for activities conducted with cannabis extract or edible cannabis</li><li>Responsible for approval of methods and procedures related to GPP</li><li>Preparing representative batch samples for lab testing and retention.</li><li>Configuring and monitoring seed-to-sale software (Ample Organics).</li><li>Reporting to senior management.</li><li>Identify and investigate deviations and perform corrective and preventative actions.</li></ul><p><b>Required Qualification</b></p><p><b>Formal Education or Equivalent: </b></p><ul><li>Science degree or equivalent</li><li>Quality Assurance Certificate an asset</li><li>The technical knowledge, experience, and training to fulfill the responsibilities as required by Health Canada Cannabis Regulations</li><li>Previous quality assurance experience in cannabis, pharmaceuticals, medical or food production required.</li><li>HACCP training/certificate is an asset.</li></ul><p><b>Years of Experience: </b></p><ul><li>2-5 years in a quality assurance role at a licensed cannabis producer is an asset.</li></ul><p><b>Competencies, Specialized Skills or Knowledge unique to this role: </b></p><ul><li>Previous quality assurance experience in cannabis is an asset.</li><li>Security Clearance will be required for this position. Previous security cleared status is an asset.</li><li>Must be qualified to be the Alternate Quality Assurance Person under Health Canada requirements.</li></ul><p><b>Performance Metrics</b> ·</p><ul><li><i>Professionalism</i>: Meeting compliance with regulations at all times</li><li><i>Communication: </i>Lead HC inspections with efficiency and politeness.</li><li><i>Accountability: </i>Identifying and taking preventive measures in response.</li><li><i>Learning &amp; Development: </i>Training new hires on SOP’s and re-training expectations.</li><li><i>Flexibility: </i>Keeping up to date with HC regulations and ensuring SOP meet the requirements.</li><li><i>Efficiency: </i>Reviewing and executing records upon completion.</li><li><i>Leadership: </i>Coaching staff on Health Canada Compliance.</li></ul><p><b>Physical requirements</b></p><ul><li>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</li><li>Ability to lift, push, and pull 50 pounds</li><li>Ability to sit, squat, bend, and kneel repetitively throughout an 8 or 10-hour day</li><li>Ability to stand and walk for extended periods of time</li><li>Ability to visually identify plant health issues, safety hazards, and signage</li><li>§ Ability to use a ladder up to 12-20 feet high</li></ul><p><b>Expected Hours of Work; </b>This is a full-time position that requires but is not limited to, 40 hours per week. Operational hours are dependent on the client and facility operations. This position may be required to work weekends and holidays.</p><p>The Quality Assurance Technician will report to the Quality Assurance Manager.</p><p>Have reliable transportation to and from the facility.</p><p><b>Environmental Conditions</b></p><ul><li>The QA Technician may be exposed to pollen, allergens, and chemical pesticides at the facility. As well as fumes, dust, odors, extreme heat temperatures, heights, indoor AC, no AC, motion, noise, protective gear, vibrations, and water.</li></ul><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Employee assistance program</li><li>Extended health care</li><li>Life insurance</li><li>On-site parking</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>10 hour shift</li><li>8 hour shift</li><li>Day shift</li><li>Holidays</li><li>Monday to Friday</li><li>On call</li><li>Overtime</li><li>Weekends</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"name":"AtlantiCann Medical Inc"},"location":{"country":"Canada","address":"Lower Sackville, NS","city":"Lower Sackville","stateProvince":"NS"},"frontendLink":"/job-posting/atlanticann-medical-inc/quality-assurance-technician/63fe4096fbcf58245c4054870e794769","title":"Quality Assurance Technician","hash":"63fe4096fbcf58245c4054870e794769","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-8e5fa67d73c976b9"},{"employmentType":"Full-time, Permanent","postedOn":"9 days ago","description":"<div><p><i>Quality Control Technician</i><br />We are looking for a well-organized, detail-oriented individual to join our quality team. This individual will work in collaboration with all of the departments to promote a culture of continuous improvement.</p><p>Responsibilities:</p><ul><li>Perform in-process control monitoring such as swabbing equipment and rooms for micro contamination, water testing, air quality testing, environmental control verification, equipment calibration, pest control</li><li>Track and analyse all test results to determine process effectiveness and optimization</li><li>Inspection of in process and finished product</li><li>Preparation of lot release reports</li><li>Preparation of cannabis samples to be transferred to approved 3rd party testing laboratories</li><li>Identify non-conformities, determine appropriate corrective and preventive action</li><li>Assist with all laboratory tasks, laboratory equipment management, method validations, microbiology, cannabinoid potency, moisture analysis, foreign material inspection</li><li>Assist in authoring and updating Standard Operating Procedures to support Good Manufacturing Practices</li><li>Ensure all documentation and processes are approved by the Quality Assurance Person</li><li>Assist with quality investigations when required</li><li>Maintain understanding of all procedures and applicable regulations</li><li>Support Health Canada Inspections</li><li>Assist in preparation and management of future Extraction Division</li><li>Other duties as assigned</li></ul><p>Education:</p><ul><li>Minimum College diploma/ Bachelor’s degree or equivalent in related scientific field with regulatory discipline required</li><li>1-2 years of education and/or experience in microbiology/chemistry preferred</li></ul><p>Other:</p><ul><li>Understanding of sampling protocols, sampling plans, test methodology, test method limitation, validation, and risk assessment analysis an asset</li><li>QC experience in a GMP-focused quality related position or experience in cannabis industry environment is an asset</li><li>This is a full time position</li><li>Will be required to complete security clearance/ police check</li></ul><p>Job Types: Full-time, Permanent</p><p>Salary: $18.00-$22.00 per hour</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Extended health care</li><li>Life insurance</li><li>On-site parking</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Day shift</li><li>Holidays</li><li>Monday to Friday</li><li>Overtime</li></ul><p>COVID-19 considerations:<br />Daily screening and temperature check upon entering facility. Mask, Face Shield, scrubs and gloves required. Social distancing and cohorts in place. Frequent cleaning and sanitizing of common areas.</p><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Muskoka Grown","logoUrl":"/logos/muskoka-grown-7cb5a54b423f6197f4ba70709ad76a65.jpeg"},"location":{"country":"Canada","address":"Bracebridge, ON","city":"Bracebridge","stateProvince":"ON"},"frontendLink":"/job-posting/muskoka-grown/quality-control-technician/873b74f0e9bb06d4809f6399af10f762","title":"Quality Control Technician","hash":"873b74f0e9bb06d4809f6399af10f762","postingUrl":"https://ca.indeed.com/job/quality-control-technician-84c19335448c1e3c"},{"postedOn":"13 hours ago","description":"<div><div>Cronos Group is an innovative global cannabinoid company with international production and distribution across five continents. Cronos Group is committed to building disruptive intellectual property by advancing cannabis research, technology and product development. With a passion to responsibly elevate the consumer experience, Cronos Group is building an iconic brand portfolio. Cronos Group’s portfolio includes PEACE NATURALS™, a global health and wellness platform, two adult-use brands, COVE™ and Spinach™, and two hemp-derived CBD brands, Lord Jones™ and Happy Dance™.<br /><br />At Cronos Group, we hire talented people who thrive on solving difficult problems and give them the opportunity to hone new skills and approaches. If you want to play a part in shaping an innovative industry and help build a historically significant company, we want to meet you.<br /><br />As the QA Specialist, you will work within the Quality Assurance/ Control department and report to the QA Manager. You will complete tasks related to monitoring, testing, reporting, and ensuring quality of cannabis product and processes with the Peace Naturals Quality Management System (QMS). This position supports in the area of: GMP equipment and process validation testing, calibration requirement, monitoring of process control methods and parameters, finished product quality and customer satisfaction.<br /><br />This position is based out of Stayner, Ontario Canada<br /><br /><b>What you’ll be doing:</b><br /><ul><li>Maintaining compliance with the laws and regulations related to medical cannabis</li><li>Develop and execute procedures and processes to support Quality Management System</li><li>Experience with the use of statistical analysis software</li><li>Lead problem solving teams using quality principals and tools for root cause analysis, corrective actions, verification and effectiveness</li><li>Development and control of quality plans, inspection instructions for in-coming, in-process and final inspection</li><li>Responsible for continual improvement activities to enhance the quality system, such as 5S, kaizen lean methods, etc</li><li>Completing and preparing appropriate documentation as required i.e. reports, authoring SOPs, Work Instructions</li><li>Investigate and resolve deviations ensuring follow up and appropriate supporting documentation is completed. Topics include but are not limited to product failure, critical deviation, and other occurrences</li><li>Review and assess impact of changes to compliance for manufacturing, testing, and packaging</li><li>Perform internal audits as assigned according to Cronos audit program to ensure compliance to GPP/GMP &amp; internal requirements. Complete reports and file all supporting documentation</li><li>Develop quality control plans, inspection instructions for incoming, in-process and final inspection.</li><li>Participate in regulatory and customer audits as required</li><li>Support the management of records and records activities</li><li>Work as a member of a team to achieve all outcomes. Develop a working interaction with all operation groups to ensure discrepancy resolution and improvement of company practices</li><li>Perform all work in accordance with all established regulatory, compliance and safety requirements. Report and correct unsafe acts and conditions</li><li>Data Collection, Analysis and Reporting</li><li>Review completed batch production records before release for sale to ensure compliance with GPP, SOPs, specifications and approved current master production documentation</li><li>Conduct gap assessment between GMP/GPP regulations and current operational practices</li><li>Recommend Quality Assurance best practices and help define and champion Quality Assurance standards</li><li>Ensure that all duties are carried out effectively and proficiently, in a timely and professional manner, and with diligent attention to quality of work</li></ul><br /><b>Your Environment:</b><br /><ul><li>50/50 split between desk work and working in the production rooms</li><li>Sitting for long periods of time</li><li>Manual dexterity required to use desktop computer and peripherals</li><li>In production: warm, humid environment with bright lights</li><li>Exposure to pollen, allergens, approved pesticides, chemical vapors, odors and dust</li></ul><br /><br /><b>You’ll need to have:</b><br /><ul><li>Post-Secondary education in relevant field</li><li>ASQ certifications is considered an asset</li><li>3+ years’ experience in a similar position</li><li>Advanced level experience in Microsoft Excel, Word and PowerPoint</li><li>Experience working in quality control/lab and utilizing scientific equipment</li><li>Problem Solving, Project Management and strong communication skills</li><li>Background in developing and managing KPIs (Key Performance Indicators)</li><li>Excellent verbal and written communication skills</li><li>Able to support overtime and weekend work at short notice</li></ul><br /><i>We are committed to fostering a diverse and inclusive work environment, and we welcome and encourage applications from people with disabilities and people with diverse backgrounds, identities, and cultures. For candidates with disabilities, accommodations are available upon request in all phases of the selection process.</i></div></div>","company":{"companyType":"Public/Established","name":"Cronos Group Inc.","logoUrl":"/logos/cronos-group-47b857beff34185df81846a0ae6bb359.png"},"location":{"country":"Canada","address":"Stayner, ON","city":"Stayner","stateProvince":"ON"},"frontendLink":"/job-posting/cronos-group-inc/qa-specialist/2bd4b968d71b6dc795337b80cf7c8492","title":"QA Specialist","hash":"2bd4b968d71b6dc795337b80cf7c8492","postingUrl":"https://ca.indeed.com/job/qa-specialist-0b31bc5b71856c7c"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p><i>Senior Quality Assurance Associate </i><br />The Senior Quality Assurance Associate is responsible for supporting the Head of Quality Assurance &amp; Quality Control in assuring the quality of dried cannabis, cannabis oil and cannabis oil capsules (“product(s)”) before they are made available for sale. Additionally, the QA Associate Manager is responsible for supporting the Head of QA/QC in assuring compliance with the Controlled Drug and Substances Act and the Cannabis Act .</p><p><b>Responsibilities: </b></p><p>· Supervise Quality Assurance Associate in assuring compliance with Controlled Drug and Substances Act, Cannabis act and Food &amp; Drugs Act.<br />· Perform in-process testing and inspection during cultivation, processing and packaging.<br />· Ensure product is sampled for outside lab testing.<br />· Coordinate the delivery of samples to outside labs for product testing<br />· Manage the retain sample program.<br />· Review batch records, sanitation records, test records, environmental monitoring records and any non-conformance reports for batch disposition (release/rejection)<br />· Perform air and surface sampling for the environmental monitoring program<br />· Coordinate the processing of environmental samples with contract labs.<br />· Review environmental sample reports from contract labs<br />· Prepare and review SOPs as required.<br />· Manage the change control, non-conformance and planned deviation processes<br />· Ensure that investigations are performed as per SOP and any corrective action is completed in a timely fashion.<br />· Manage the training program and distribution of SOPs within the facility.<br />· Act as alternative QAP in the absence of appointed QAP.<br />· Assist the Head of QA/QC in the event of a recall<br />· Assist the Head of QA/QC during regulatory and customer audits and inspections.<br />· Assist the Head of QA/QC in the investigation of complaints.<br />· Assist the Head of QA/QC during the inspection of vendors.<br />· Assist the Head of QA/QC in Good Production Practice training of employees.<br />· Audit cultivation, processing, sanitation and maintenance practices against RMMI SOPs.<br />· Perform other duties as required</p><p><b>Qualifications: </b></p><p>· B.Sc. degree in Plant Science, Biology, Microbiology, Chemistry or a similar discipline.<br />· Cannabis Security Clearance required.<br />· Food, agricultural or pharmaceutical quality assurance work experience is desirable.<br />Excellent communication skills, both written and oral, are required.</p><p><b>Work Conditions: </b></p><ul><li>Repetitive work</li><li>Manual dexterity required to use desktop computer and peripherals</li><li>Will be in contact with Cannabis and its components (THC, CBD and Pollen)</li><li>Working in a busy environment with frequent interruptions</li><li>Use of required personal protective equipment</li><li>Overtime/Weekend Coverage as required</li></ul><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Dental care</li><li>Disability insurance</li><li>Extended health care</li><li>Paid time off</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>Monday to Friday</li><li>Weekends</li></ul><p>Education:</p><ul><li>Bachelor's Degree (preferred)</li></ul><p>Experience:</p><ul><li>Quality assurance: 3 years (preferred)</li><li>Cannabis/Pharmaceutical/Food QA: 2 years (preferred)</li></ul></div>","company":{"companyType":"Public/Growth","name":"Radicle Medical Marijuana Inc","logoUrl":"/logos/medical-marijuana-inc-22e8a48e0aa659773940d2bf3ea13b8a.jpeg"},"location":{"country":"Canada","address":"Hamilton, ON","city":"Hamilton","stateProvince":"ON"},"frontendLink":"/job-posting/radicle-medical-marijuana-inc/senior-quality-assurance-analyst/80cae3fdb8481b9eca39f0daa0c8c7f4","title":"Senior Quality Assurance Analyst","hash":"80cae3fdb8481b9eca39f0daa0c8c7f4","postingUrl":"https://ca.indeed.com/job/senior-quality-assurance-analyst-713bcba8944b0f8b"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p>Quality Control Technicians are responsible for the efficiency and quality of cannabis by trimming, manicuring and preparing product for sale. We are currently seeking motivated, dependable people to fill entry level positions into the medical cannabis industry. Must have reliable transportation. Must be able to stand for long periods of time. Hiring Immediately. No experience required.</p><p>Duties and Responsibilities:</p><p>-Responsible for trimming (minimum of 1/2 pound per hour) and manicuring cannabis in a timely, efficient manner to prepare product for sale.</p><p>-Working respectfully and collectively with other Quality Control team members</p><p>-Follow all safety regulations set by team leaders</p><p>-Ensure consistent quality</p><p>-Ensure an overall positive, safe and clean environment</p><p>Qualifications:</p><p>-Must be able to pass state and federal background checks</p><p>-Experience and knowledge in manufacturing / laborer industry preferred but not required</p><p>-Ability to work in a fast paced environment</p><p>-Ability to handle high stress situations</p><p>-Self Motivated</p><p>-Ability to multi-task</p><p>-Must be at least 21 years of age and authorized to work in the US.</p><p>-Must be willing to work 7 days a week if necessary, and to be flexible with schedule.</p><p>-Ability to work 4 10 hour shifts</p><p>-Exposure to fertilizer, dusts, odors, allergens, pollen, and other environmental variables.</p><p>Education:</p><p>-Minimum High School or G.E.D. equivalent required</p><p>Benefits:</p><ul><li>Private medical/dental insurance</li><li>Life insurance</li></ul><p>Job Type: Full-time</p><p>Pay: $14.00 - $16.00 per hour</p><p>COVID-19 considerations:<br />Follows all COVID-19 protocol.</p><p>Edit job<br />Status: Open<br />View public job page</p><p>Details<br />Created: January 5, 2021<br />Views: 1,547<br />Curated Candidates: 180 total<br />Add a candidate<br />Find candidates</p><p>Budget<br />Job Budget: Not sponsored<br />Sponsor job</p><p>Job Type: Full-time</p><p>Pay: $14.00 - $16.00 per hour</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>COVID-19 considerations:<br />We adhere to all COVID-19 protocols and precautions.</p><p>Application Question(s):</p><ul><li>Are you at least 21 years of age and authorized to work in the US?</li></ul><p>Education:</p><ul><li>High school or equivalent (Preferred)</li></ul><p>Experience:</p><ul><li>Manufacturing: 1 year (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Established","name":"NSMC"},"location":{"country":"United States","address":"White Hall, AR 71602","city":"White Hall","stateProvince":"AR"},"frontendLink":"/job-posting/nsmc/quality-control-technician/1ffe5ac72987e4252f45082685422b80","title":"Quality Control Technician","hash":"1ffe5ac72987e4252f45082685422b80","postingUrl":"https://www.indeed.com/job/quality-control-technician-95ac25f681fe3af9"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p>Job Title: Food Safety/Quality Assurance Technician - Nights</p><p>Department: Processing</p><p>Reports to: QA Supervisor/Team Lead</p><p>FLSA Status: Regular Full-Time</p><p>Salary: Hourly</p><p>Location: Midway, Fl</p><p>Role Summary</p><p>Maintains food safety and quality standards and effective documentation to ensure the company is following best practices for food safety and quality. The FS/QA Technician reports to the Food Safety Manager.</p><p><b>Key Duties and Responsibilities:</b></p><p>Responsible for maintaining the safety, legality and quality of each food and the processes used in their manufacture according to applicable regulations</p><p>Responsible for testing, monitoring, and documentation of the Quality Systems including procedures, records, Good Manufacturing Practices (GMPs), Hazard Analysis Critical Control Points (HACCP), Preventive Controls (PCs), Sanitation Standard Operating Procedures (SSOPs), etc.</p><p>• Perform pre-operative procedures, and environmental monitoring swabs as applicable</p><p>• Maintain and organize quality and production documentation</p><p>• Reports food safety and quality issues to supervisors, performing corrective actions as necessary</p><p>• Provide coverage for quality employees when necessary.</p><p>• Analyze/inspect food items at specified stages in the production process for compliance to specification</p><p>• Able to use and calibrate/verify the following instrumentation/measuring devices: Thermometers, Metal detectors, Calculators and Scales.</p><p>• Approves in-process production and finished products by confirming specifications; conducting visual and measurement tests; communicating required adjustments to production supervisor.</p><p>• Documents inspection results by completing reports and logs; summarizing re-work and waste; inputting data into quality database.</p><p>• Keeps measurement equipment operating by following operating instructions, calling for repairs.</p><p>• Maintains safe and healthy work environment by following standards and procedures, complying with legal regulations.</p><p>• Updates job knowledge by participating in educational opportunities; reading technical publications.</p><p>• All other duties as required</p><p><b>SKILLS AND QUALIFICATIONS:</b></p><p>• Food Handling/Safety Experience Preferred</p><p>• Analyzing Information</p><p>• Reporting Research Results</p><p>• Documentation Skills</p><p>• Promoting Process Improvement</p><p><b>ADDITIONAL REQUIREMENTS:</b></p><p>• Florida Driver's License or ability to obtain one.</p><p>• Per state law, must be a minimum of 21 years of age.</p><p>• Must be and remain compliant with any and all legal or company regulations for working in the cannabis industry.</p><p>• Must successfully complete a comprehensive background check.</p><p><b>PHYSICAL REQUIREMENTS:</b></p><p>• Must be able to push, pull, move, and/or lift a minimum of 40lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistance</p><p>• Must be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stopping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasks</p><p>• Must be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater)</p><p>• Must have visual acuity with/without job aids to perform activities such as; reading, viewing a computer terminal, visual inspection involving small parts/details. Clarity of vision at 20 ft or more in day and night/dark conditions</p><p>• Must be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc. (Moderate noise)</p><p><b>WORK SCHEDULE:</b></p><p>• 40+ hours weekly with flexible hours depending on department needs. Must be available to work occasional evenings, weekends, and holidays</p><p>Equal Opportunity Employer l Trulieve Supports a Drug Free Workplace</p></div>","company":{"website":"trulieve.com","companyType":"Public/Established","name":"Trulieve","logoUrl":"/logos/trulieve-1d76a294c42e35e1fad949d6f74742d9.png"},"location":{"country":"United States","address":"Midway, FL, USA","city":"Midway","stateProvince":"FL"},"frontendLink":"/job-posting/trulieve/food-safety-quality-assurance-technician/54e698fd4670281d6c39577671bcfaba","title":"Food Safety Quality Assurance Technician","hash":"54e698fd4670281d6c39577671bcfaba","postingUrl":"https://jobs.leafwire.com/job/uf6gtj/food-safety-quality-assurance-technician/midway/fl/united-states"},{"employmentType":"Full-time, Permanent","postedOn":"10 days ago","description":"<div><p><i>Quality Assurance/Control Supervisor </i><br />Under the direction of the Quality Assurance Manager, the Quality Assurance/Control Supervisor is primarily responsible for the monitoring and quality control of cannabis production and processing within the facility. The role will also be responsible for ensuring compliance with the Cannabis Act and Good Production Practices (GPP). The Quality Assurance/Control Supervisor will be able to communicate with management and production team effectively. They will be energetic and a team player by excellence.</p><p><b>Job Duties: </b></p><ul><li>Ensure that Quality Assurance and Production Standard Operating Procedures are strictly followed and enforced.</li><li>Continuous SOP revisions, creation of new Standard Operating Procedure’s and protocols through the internal Quality Management Software.</li><li>Supporting in implementation and training of current SOP’s.</li><li>Update, develop and implement logs for Quality Assurance Operations.</li><li>Ensure compliance with Cannabis Act and Cannabis Regulations.</li><li>Familiar with Cannabis Regulations, Controlled Substances Act. Pest Control Act, Food and Drug Act and Ontario Health and Safety Act.</li><li>Collaborate with other departments to ensure compliance with standard operating procedures.</li><li>Implement GPP within the production environment, develop and implement quality documents.</li><li>Perform in-process QA inspections and ensure that all activities within production area are executed as per defined SOPs.</li><li>Conduct QC internal tests as ATP Swabs Testing, Moisture Content of in process/final product and create reports in compliance with companies’ policies, practices, and procedures.</li><li>Conduct inspection and approval of in-coming materials for production and ensure they are by approved by Quality before usage.</li><li>Perform product sampling and coordinate product testing with the approved testing lab.</li><li>Assist in development of Corrective and Preventative Actions as per production process.</li><li>Perform any other tasks assigned by the management.</li><li>Familiar with Quality Management Software-Microsoft Enterprise Cloud.</li><li>Develop an internal calibration program of equipment in Good Production Practices areas and maintain external calibration data and documentation.</li><li>Develop and assist in internal auditing/inspection program.</li></ul><p><b>Requirements: </b></p><ul><li>1-5 years of work experience in a quality assurance role in pharmaceutical, food, cosmetics or related industry.</li><li>Post-secondary degree or diploma in biological science (chemistry, plant biology, pharmacology).</li><li>1+ years working in the cannabis industry.</li><li>Cannabis Act and other cannabis regulations knowledge is an asset.</li><li>Experience with an organization regulated by Health Canada or experience in a similarly regulated environment (GPP, GMP, GAP).</li><li>Ability to follow strict operating procedures.</li><li>Ability to work individually as well as part of a team.</li><li>Ability to adapt to new technologies.</li><li>Dedication to safety measures and best practices.</li><li>Ability to prioritize and manage conflicting demands.</li><li><b>Must have, or be able to obtain a HEALTH CANADA Security Clearance. Those with current security clearance will be given priority for the role.</b></li></ul><p><b>Job Conditions: </b></p><ul><li>Will be in contact with Cannabis and its components/derivatives.</li><li>Use of required personal protective equipment.</li></ul><p>Job Types: Full-time, Permanent</p><p>Salary: $40,000.00-$60,000.00 per year</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Disability insurance</li><li>Extended health care</li><li>Life insurance</li><li>On-site parking</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Day shift</li><li>Monday to Friday</li><li>On call</li><li>Weekends</li></ul><p>Education:</p><ul><li>Bachelor's Degree (required)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 1 year (required)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private","name":"THPC"},"location":{"country":"Canada","address":"Brantford, ON","city":"Brantford","stateProvince":"ON"},"frontendLink":"/job-posting/thpc/quality-control-supervisor/55291565431a8013b419f17c21067a3f","title":"Quality Control Supervisor","hash":"55291565431a8013b419f17c21067a3f","postingUrl":"https://ca.indeed.com/job/quality-control-supervisor-4b07a7f3d3811245"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>Job Title: Quality Assurance Technician</p><p>Department: Quality Assurance</p><p>Reports to: QA Supervisor or Team Lead</p><p>FLSA Status: Regular Full-Time</p><p>Salary: Hourly</p><p>Location: Midway, Fl</p><p>Role Summary</p><p>The Quality Assurance Technician is responsible for conducting visual scans on products in effort to assure quality and safety of products intended for consumers. QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on. Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans.</p><p><b>Key Duties and Responsibilities:</b></p><p>• Conduct visual inspections of cannabis for organic and inorganic adulterants and defects.</p><p>• Document inspection results by completing reports and logs and inputting data into quality database.</p><p>• Keep equipment (i.e. scales, tools, etc) in good, working order.</p><p>• Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulations</p><p>• Maintains and ensures that proper PPE is utilized and changed out regularly, or as needed</p><p>• Provide Feedback as needed</p><p>• Performs other duties as required</p><p><b>SKILLS AND QUALIFICATIONS:</b></p><p>• High School Diploma or GED</p><p>• Detail Oriented</p><p>• Coachable and a willingness to learn</p><p>• Ability to work in a fast-paced environment</p><p>• Ability to focus and avoid distractions</p><p>• Comfortable operating digital scales</p><p>• Basic computer knowledge</p><p>• Basic math and reading comprehension</p><p>• Organizational skills</p><p><b>ADDITIONAL REQUIREMENTS:</b></p><p>• Florida Driver's License or ability to obtain one.</p><p>• Per state law, must be a minimum of 21 years of age.</p><p>• Must be and remain compliant with any and all legal or company regulations for working in the cannabis industry.</p><p>• Must successfully complete a comprehensive background check.</p><p><b>PHYSICAL REQUIREMENTS:</b></p><p>• Must be able to push, pull, move, and/or lift a minimum of 40lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistance</p><p>• Must be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stopping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasks</p><p>• Must be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater)</p><p>• Must have visual acuity with/without job aids to perform activities such as; reading, viewing a computer terminal, visual inspection involving small parts/details. Clarity of vision at 20 ft or more in day and night/dark conditions</p><p>• Must be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc. (Moderate noise)</p><p><b>WORK SCHEDULE:</b></p><p>• 40+ hours weekly with flexible hours depending on department needs. Must be available to work occasional evenings, weekends, and holidays</p><p>Equal Opportunity Employer l Trulieve Supports a Drug Free Workplace</p></div>","company":{"companyType":"Public/Established","name":"Trulieve, INC","logoUrl":"/logos/trulieve-1d76a294c42e35e1fad949d6f74742d9.png"},"location":{"country":"United States","address":"Midway, FL, USA","city":"Midway","stateProvince":"FL"},"frontendLink":"/job-posting/trulieve-inc/quality-assurance-technician-day-shift/a19073b36a8273d9428f16a376937bcb","title":"Quality Assurance Technician - DAY Shift","hash":"a19073b36a8273d9428f16a376937bcb","postingUrl":"https://www.glassdoor.com/job-listing/quality-assurance-technician-day-shift-trulieve-JV_IC1154372_KO0,38_KE39,47.htm?jl=4028985272"},{"employmentType":"Full-time","postedOn":"10 days ago","description":"<div><p>Reporting to the CEO and other senior-level management, the Quality Assurance Person (QAP) is the Quality Assurance Manager within the licensed site. The QAP is responsible for the verification and validation of quality assurance, ensuring that cannabis products produced meet the organization’s objectives for quality, safety, regulatory, and customer expectations in accordance with the Cannabis Act and relevant regulations.</p><p>The QAP will advise on, establish and monitor quality management systems and coordinate activities to meet production process and product quality standards for the outdoor cultivation and processing facility.</p><p>This role will require being onsite in Whitehorse, Seasonally (May-November) with year-round QAP responsibility. Relocation will be supported for this position.</p><p><b>Responsibilities:</b></p><p>• Manage the licensed site’s Quality Assurance Department and lead in developing, reviewing, and maintaining SOPs &amp; quality management programs and projects to ensure compliance under the Cannabis Act/Regulations. Work cross-departmentally to implement SOPs (i.e. operations, regulatory, security).</p><p>• Develop training programs around SOPs pertaining to GPP and record-keeping compliance.</p><p>• Create quality control programs/systems for cannabis storage.</p><p>• Develop programs around GPP &amp; record-keeping methods for sanitation of premises, equipment, cleanliness, hygienic behavior of personnel, and facility maintenance.</p><p>• Establish and maintain record-keeping systems and ensure employee adherence to proper documentation practices.</p><p>• Conduct testing on each lot or batch of cannabis prior to release for sale; ensure testing is conducted using validated methods, investigating deviations and out-of-spec results.</p><p>• Develop and perform internal audits regularly to determine quality assurance compliance according to Cannabis Regulations.</p><p>• Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary.</p><p>• Maintain current knowledge of best practices for the provisions of the Cannabis Act and Cannabis Regulations that apply to the license holder.</p><p><b>Required Responsibilities as per Cannabis Regulations:</b></p><p>• Function as QAP to support in all matters relating to Good Production Practices (GPP) and record-keeping compliance during Health Canada inspections.</p><p>• Review and approve methods and procedures pertaining to Cannabis Regulations within the licensed site.</p><p>• Investigate complaints regarding the quality of cannabis production and ensure immediate corrective action when necessary; take corrective and preventative measures.</p><p>• Ensure cannabis quality meets standards prior to release for sale.</p><p>• Submit, secure and maintain a valid security clearance.</p><p><b>Qualifications:</b></p><p>• Degree in Chemistry, Biology, Pharmacology or Food Science, obtained or recognized by a Canadian university.</p><p>• 5+ years’ senior management experience in Quality Assurance/Control in a production environment.</p><p>• Valid HC security clearance (or ability to obtain one).</p><p>• Solid ERP, eQMS, CTLS reporting experience.</p><p>• Proven knowledge and experience in the stated responsibilities of the position (i.e. Food, Pharma, NHP).</p><p>• Previous experience as a stand-alone QA/QC resource having direct responsibility for determining strategic objectives to meet quality with given resources and carry out tactical execution.</p><p>• Preferred experience with cGMP, GAP, GLP, HACCP, ISO, and FDA</p></div>","company":{"companyType":"Private/Startup","name":"Cannabis At Work","logoUrl":"/logos/cannabis-at-work-8ae63b190226a7031617f4393f916a20.jpeg"},"location":{"country":"Canada","address":"Whitehorse, YT","city":"Whitehorse","stateProvince":"YT"},"frontendLink":"/job-posting/cannabis-at-work/quality-assurance-person/e9aa83314b15b327959f16e08d2a8c07","title":"Quality Assurance Person","hash":"e9aa83314b15b327959f16e08d2a8c07","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-person-at-cannabis-at-work-2519093629"},{"employmentType":"Full-time","postedOn":"10 days ago","description":"<div><p><b>Summary: </b></p><p>The Junior Quality Assurance Person will be responsible for assisting in the coordination of work to ensure the successful implementation of Cannabis Act, Cannabis Regulations, Good Manufacturing Practices (GMP) and Good Production Practices (GPP) production standards in pursuance of regulatory compliance and achievement of business goals. The QAP will work hand in hand with production, maintenance, facilities and shipping teams to ensure that quality standards are recognized, implemented, enhanced and maintained throughout all of production operations.</p><p><b>Key Responsibilities: </b></p><ul><li>Provides oversight on the performance of all Quality Assurance (QA) personnel, practices, and procedures</li><li>Serves as the Health Canada Compliance Manager and one of the primary contracts for Health Canada</li><li>Initiates the development and ongoing amendment of the organization’s Standard Operating Procedures (SOPS)</li><li>Serves as the internal compliance auditor ensuring the organization’s compliance with all regulatory rules and regulations</li><li>Ensures that the QA practices at each of the organization’s facilities align with the company’s business plan and GMP/GPP standards</li><li>Develops and executes product quality and yield improvement strategies</li><li>Assures regulatory requirements are embodied in all of the organization’s policies, directives, practices, processes and forms</li><li>Establishes and maintains product quality documentation by writing and updating quality assurance procedures</li><li>Establishes the following quality and reliability standards by studying their respective requirements, processes, and procedures:</li><li>Raw material standards</li></ul><p>o In-process product inspection standards<br />o Standards for the disposition of finished products<br />o Rework standards</p><ul><li>Maintains and improves product quality by enforcing QA policies and procedures and government requirements; completing product, company, system, and compliance audits; investigating customer complaints; and collaborating with members of senior management to develop new product and engineering designs as well as manufacturing and training methods</li><li>Develops QA plans by conducting hazard analyses; identifying critical control points and preventative measures; establishing critical limits, monitoring procedures, corrective actions and verification procedures</li><li>Prepares product and process quality reports by collecting, analyzing and summarizing information and trends</li><li>Assists in regulatory submission activities from the development/investigational stage through to filing, approval, and post market submissions</li><li>Develops regulatory strategies for current and future programs in collaboration with other senior management</li><li>Provides expertise and support to regulatory inspections including quality representation on all activities</li><li>Develops, updates, and maintains quality systems and manuals that comply with the Cannabis Regulations, Cannabis Act, and GMP/GPP standards</li><li>Investigates product non-conformances; reviews material, document findings and responses for complaints. Manages product holds, reprocessing actions, and final disposition processes for non-compliant resources</li><li>Enforces regulatory requirements in addition to reading and being familiar with the organization’s security directives</li><li>Directs activities of the Quality Assurance department which support the company’s quality vision</li><li>Maintains QA staff by working the Human Resources Manager to recruit, select, orientate, and train of the department employees</li><li>Participates in developing quality metrics and goals, leading efforts in rolling them out to the organization’s facilities</li><li>Provides guidance on production processes where applicable, including troubleshooting, GMP/GPP compliance, and control of contaminants</li><li>Communicates with Operations and Production Technology Manager and relevant facility staff including Master Growers and Quality Assurance personnel</li><li>Ensure investigation and annual product review are conducted in a compliant matter</li></ul><p><b>Qualifications: </b></p><ul><li>BSc/MSc in Chemistry/Biochemistry/Biology/Food or similar discipline. MSc is preferred.</li><li>3-5 years of experience in a QA/Regulatory manufacturing environment.</li><li>Existing CTLS security clearance for QAP.</li><li>Experience in managing Quality Management Systems and creating Preventative Control Plans</li><li>Strong understanding of Health Canada, and GMP/GPP requirements for pharmaceutical, health, food processing, and cannabis products.</li></ul><p>Job Type: Full-time</p><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Choice Growers","logoUrl":"/logos/choice-cannabis-727bb8f333cd8f62c23ce3298e046e32.png"},"location":{"country":"Canada","address":"Strathmore, AB","city":"Strathmore","stateProvince":"AB"},"frontendLink":"/job-posting/choice-growers/junior-quality-assurance-person/f3ab881b92f46fcdf1b8e4576032dca1","title":"Junior Quality Assurance Person","hash":"f3ab881b92f46fcdf1b8e4576032dca1","postingUrl":"https://ca.indeed.com/job/junior-quality-assurance-person-c3464f7c888c1048"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p><b>Quality Assurance Technician - NIGHT ShiftDescriptionJob Title:</b></p><p><b>Quality Assurance Technician - Nights 12 Hour Rotating ShiftDepartment:</b></p><p><b>Quality AssuranceReports to:</b></p><p><b>QA Supervisor or Team LeadFLSA Status:</b></p><p><b>Regular Full-Time Salary:</b></p><p><b>HourlyLocation:</b></p><p>Midway, FlRole SummaryThe Quality Assurance Technician is responsible for conducting visual scans on products in effort to assure quality and safety of products intended for consumers.</p><p>QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on.</p><p><b>Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans.Key Duties and Responsibilities:</b></p><p>Conduct visual inspections of cannabis for organic and inorganic adulterants and defects.Document inspection results by completing reports and logs and inputting data into quality database.Keep equipment (i.e.</p><p><b>scales, tools, etc) in good, working order.Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulationsMaintains and ensures that proper PPE is utilized and changed out regularly, or as neededProvide Feedback as neededPerforms other duties as requiredPosition RequirementsSKILLS AND QUALIFICATIONS:</b></p><p><b>High School Diploma or GEDDetail OrientedCoachable and a willingness to learnAbility to work in a fast-paced environmentAbility to focus and avoid distractionsComfortable operating digital scalesBasic computer knowledgeBasic math and reading comprehensionOrganizational skillsADDITIONAL REQUIREMENTS:</b></p><p><b>Florida Driver's License or ability to obtain one.Per state law, must be a minimum of 21 years of age.Must be and remain compliant with any and all legal or company regulations for working in the cannabis industry.Must successfully complete a comprehensive background check.PHYSICAL REQUIREMENTS:</b></p><p>Must be able to push, pull, move, and/or lift a minimum of 40lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistanceMust be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stopping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasksMust be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater)Must have visual acuity with/without job aids to perform activities such as; reading, viewing a computer terminal, visual inspection involving small parts/details.</p><p>Clarity of vision at 20 ft or more in day and night/dark conditionsMust be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc.</p><p><b>(Moderate noise)WORK SCHEDULE:</b></p><p>40+ hours weekly with flexible hours depending on department needs.</p><p>Must be available to work occasional evenings, weekends, and holidaysEqual Opportunity Employer l Trulieve Supports a Drug Free WorkplaceShiftNights PositionQuality Assurance Technician DivisionTrulieve, INC Number of Openings8 Req NumberPRO-20-00087 Open Date1/26/2021 LocationMidway EOE StatementWe are an equal employment opportunity employer.</p><p>All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.</p><p>Marital StatusNone Specified Payroll CodeNone Specified PayNone Specified EmailNone Specified EmpI9DateNone Specified I-9 StatusNone Specified VisaNumberNone Specified Visa TypeNone Specified VisaExpiresNone Specified SuperVFlgNone Specified HoursPerWkNone Specified Compensation Plan IdNone Specified supervisorUIDNone Specified This position is currently accepting applications</p></div>","company":{"website":"trulieve.com","companyType":"Public/Established","name":"Trulieve Cannabis","logoUrl":"/logos/trulieve-1d76a294c42e35e1fad949d6f74742d9.png"},"location":{"country":"United States","address":"Midway, FL, USA","city":"Midway","stateProvince":"FL"},"frontendLink":"/job-posting/trulieve-cannabis/quality-assurance-technician-night-shift/e687de145bec4509a58c84abfd01a3e4","title":"Quality Assurance Technician - NIGHT Shift","hash":"e687de145bec4509a58c84abfd01a3e4","postingUrl":"https://www.jobilize.com/amp/job/quality-assurance-technician-night-shift-midway-trulieve-cannabis"},{"postedOn":"2 days ago","description":"<div><div><p><b>The Company</b></p><p>Open Book Extracts (OBX) is a sustainable hemp-derived cannabinoid company in the recently legalized U.S. hemp industry. The company possesses a strong leadership team with proven success in building high-growth mission-driven businesses. We are seeking talented leaders with an entrepreneurial mindset who are passionate about innovating, improving lives, and building a positive and collaborative company culture in this nascent and fast-growing sector.</p><p><b>The Position</b></p><p>The Associate Scientist will prepare, run and analyze samples for the Quality Control Laboratory utilizing HPLC and GC. In addition, the Associate Scientist will also assist QA/QC with documentation and other related tasks such as label verification and internal audits.</p><p><b>Responsibilities and Duties</b></p><ul><li>Prepare, run and analyze samples as needed using HPLC</li><li>Prepare, run and analyze samples as needed using Headspace GC-FID</li><li>Record analytical results and communicate information across functional teams</li><li>Basic troubleshooting of all analytical instrumentation and equipment</li><li>Work together with supervisor to maintain production timelines</li><li>Maintain a clean and organized work environment</li><li>Read and follow standard operating procedures and department protocols</li><li>Additional tasks as assigned by management for production and processing</li><li>Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.</li></ul><p><b>Skills and Abilities</b></p><ul><li>Previous experience with chromatography techniques</li><li>High degree of attention to detail and self-directed</li><li>High degree of mechanical aptitude</li><li>Effectively manage time by balancing multiple tasks simultaneously</li><li>Effective communication skills</li><li>Flexibility to work days/evenings/weekends depending on production schedules</li><li>Work effectively and cooperatively with others</li><li>Must be able to meet production standards in a fast-paced work environment by performing tasks quickly and efficiently</li><li>Understanding of proper and safe handling of hazardous materials</li><li>Strong documentation and computer skills</li><li>Attention to detail</li><li>Thoroughness</li></ul><p><b>Education and Experience:</b></p><ul><li>B.S. in science or related field</li><li>Experience with HPLC techniques and running analysis required</li></ul><p><b>Additional Requirements:</b></p><ul><li>This is a full-time position based out of Roxboro, NC</li><li>Flexibility to work days/evenings/weekends depending on production schedules required</li><li>Compensation commensurate with experience.</li><li>Background and reference checks required.</li></ul><p><b>Physical Demands and Working Environment:</b></p><ul><li>May be required to stand and/or walk for extended periods of time. Must be able to lift, carry and balance up to 50 pounds</li><li>While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions.</li><li>Working in limited climate-controlled facilities and experience extreme heat or cold</li><li>Work with heavy fumes, plants, airborne particles and chemicals</li><li>Must be comfortable working with and around heavy machinery</li><li>May experience moderately high noise levels</li></ul><p></p><p><b>EQUAL EMPLOYMENT OPPORTUNITY STATEMENT</b></p><p>Open Book Extracts is proud to be an equal opportunity employer. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.</p></div></div>","company":{"companyType":"Private/Established","name":"Open Book Extracts","logoUrl":"/logos/open-book-extracts-9adc75d85be33cc6d2bb6de76bfe6348.jpeg"},"location":{"country":"United States","address":"Durham, NC","city":"Durham","stateProvince":"NC"},"frontendLink":"/job-posting/open-book-extracts/qc-associate-scientist/2523163b86079e6da64cafce48d142f6","title":"QC Associate Scientist","hash":"2523163b86079e6da64cafce48d142f6","postingUrl":"https://www.indeed.com/job/qc-associate-scientist-ff5a72d24cd21edb"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p>Job titleQuality Assurance Manager Reports toChief Quality &amp; Compliance OfficerEssential Duties and Responsibilities:The Quality Assurance Manager will be the Head of Quality of the Zenabis Stellarton site in Nova Scotia, and a key member of the Site Leadership Team with dotted line reporting to the Director, Facility Operations. In this role you will be a critical leader of the Quality function, and responsible for Operational Quality, Quality Control and Quality Systems &amp; Compliance teams. You will undertake the broadest possible involvement in every aspect of cannabis production and testing, and Site operations related to the quality of products produced, and you will drive improvement activities including the development and maintenance of comprehensive quality metrics. The incumbent is responsible for the release of all products and to assure they have been produced from approved processes in conformance to all applicable regulatory requirements and Company policies.The position will partner with the manufacturing and R&amp;D organizations and support teams to make recommendations, set goals, and implement solutions for process improvements. Another key component of your role will be leveraging your ability to effectively lead a team and facilitate the learning and development opportunities for their team and the greater organization. Core CompetenciesDemonstrated subject matter expertise and knowledge of the principles and concepts of a Quality Management System (QMS)Experience leading regulatory inspections and audits.Extensive experience managing a Quality function with specifically Quality Assurance and Quality Control activitiesStrong knowledge of the Cannabis regulations, GPP and GMP standardsProven ability to lead change through an organization.Key Duties and ResponsibilitiesManages and coordinates all Quality related activities at the Stellarton site in Stellarton, Nova Scotia.Ensures compliance of QMS with Cannabis Regulations and Good Production Practices.Develops and implements programs to establish and maintain quality standards of existing products, as well as developing programs to focus employees on quality improvement. Implements policies, procedures and methods to check product, material, components and/or quality and improve same.Provides Quality leadership and direction to support business operations and develop of the site quality strategy.Provides focus on the quality status and performance of the Site by instilling a culture of quality and continuous improvement.Assures the implementation and alignment of the QMS and compliance to the pertinent national and/or global regulations.Accountable for the release of all products and to assure they have been produced from approved processes in conformance to all applicable regulatory requirements and Company policies.Ensures that all necessary testing is carried out and the associated records evaluated, in accordance with approved specifications, sampling instructions, test methods and other relevant procedures.Plans, directs, and coordinates all Quality operation activities to assure production plans are met.Responsible for day-to-day management, setting objectives, coaching and developing employees, and performance appraisal.Defines team organization and roles and responsibilities.Drives important negotiations and influences stakeholders internally.Supports interaction with strategic customers for quality requirements, incident handling and quality performance.Support interaction with regulatory authorities.Ensure that periodic internal inspections are completed to maintain the site in a compliant state.Approve signatory for major changes and New Product Introduction (NPI) reviews.Lead and manage critical quality incidents, interact with authorities and supports the Quality Operations.Perform gap assessments and lead the site implementation of corporate Quality policies.Participate in the recruitment and development of Quality staff, ensuring all team members have appropriate goals and objectives set.Actively manage the performance and development of teams using available tools and proceduresQualificationsBSc in Biological Sciences/ Pharmacy or Science related technical discipline.5+ years of hands-on experience in Quality with managerial experienceA minimum of 2 years at manager level or higher leading quality groups in a life science, GMP regulated industry.Proven experience developing teams.Experience with common continuous improvement tools (e.g., Six Sigma)Excellent written and verbal communication/ presentation skills and organizational skillsLogical in thought and detail focused.Analytical approach to problem solving and decision making.Demonstrated leadership and management experience working with cross functional teams on complex projects.Excellent negotiation skillsExperience working in a start-up Site is considered an asset</p></div>","company":{"website":"zenabis.com","companyType":"Public/Established","name":"Zenabis","logoUrl":"/logos/zenabis-8de6b1511ca7bedbbfb66faf06991126.jpeg"},"location":{"country":"Canada","address":"Stellarton, NS (+1 other)","city":"Stellarton","stateProvince":"NS"},"frontendLink":"/job-posting/zenabis/quality/2edaef8205b76ccae4bb532f3262011d","title":"Quality ...","hash":"2edaef8205b76ccae4bb532f3262011d","postingUrl":"https://ca.trabajo.org/job-850-20210506-8eb04dec0a99c019bdaf15cb04eeeea6"},{"employmentType":"Full-time","postedOn":"12 days ago","description":"<div><p>Adecco is currently looking to hire a Quality Assurance Associate for our cannabis client in Grimsby, ON. This is for an immediate start for minimum one month for $19.00/hour. The role will also be responsible for ensuring compliance with various regulations and as itpertains to the Cannabis industry as well as Good Production and ManufacturingPractices (GPP/GMP).ESSENTIAL FUNCTIONS ? Ensure that all standard operating procedures are being strictly followed at alltimes? Ensure compliance with Cannabis Regulations (CR)? Help implement and maintain GPP? Collaborate with other departments to ensure compliance with standardoperating procedures? Perform internal QA audits that are compliant with corporate policies, practices,and procedures? Adopt and incorporate quality methods into everyday work? Identify relevant QA training needs and opportunities? Conduct tests and create reports in compliance with corporate policies, practices,and procedures? Assist with the maintenance of QA monitoring programs, including audits,controls, and other qualifiers? Conduct risk analysis, verification, validation activities, and formal designreviews, as applicable? Support processes of suppliers and service providers? Ensure that refuse and cannabis products are managed or destroyed inaccordance with Cannabis Regulations (CR)? Complete inspection reports on production equipment, sanitation practices, andproduction areas? Train staff on operating procedures and GPP? Recommend corrective action? Adhere to all occupational health and safety regulations? Other duties as assignedROLE REQUIREMENTS/ABILITIES Experience / Education ? At least three years of work experience in a quality assurance role inpharmaceutical, food, or related industry? Postsecondary degree or diploma in biological science (chemistry, biology,pharmacology)? Cannabis or greenhouse industry experience would be considered an assetSkills &amp; Abilities? Knowledge of The Cannabis Act and its supporting regulations are an asset? Experience with an organization regulated by HACCP Canada or experience in asimilarly regulated environment (GMP, GAP, GPP)? Ability to follow strict operating procedures? Ability to work individually as well as part of a team? Ability to adapt to new technology? Dedication to safety measures and best practices? Ability to prioritize and manage conflicting demands? Ability to effectively communicate both verbally and in writing? High level of integrity and work ethic? Must have own transportation as we are not on a public transportation routeWorking Conditions ? Constant exposure to the smell of cannabis? Manual dexterity required to use desktop computer? Working in a busy environment with frequent interruptions? Use of required personal protective equipmentAccommodation will be provided in all parts of the hiring process as required under Adecco’s Employment Accommodation policy. Applicants will need to make their needs known in advance to their Adecco representative.I am authorized to work in Canada for any employer.* Yes No Upload or attach document from Your device Dropbox Google Drive Or Enter you work experience including both job title and job duties. Attaching your resume provides our consultants a better understanding of your work history and helps improve placement opportunities. Job Title Warehouse manager Job Duties Write about the work you’ve done and any special skills you have. I agree to the Terms of use and Application agreement.* You must agree to the Terms of use and Application agreement to proceed. Adecco is looking to hire a Sanitation Associate for our cannabis client in Grimsby, ON. This role is for an immediate start for $16/hour. The Sanitation Associate will be responsible for keeping production buildings and office building in... Adecco is currently hiring a Warehouse Associates in Burlington . The pay rate for this role is $15.00+ per hour. Please apply below as soon as possible if you are interested. Responsibilities: Receive and inspect inbound product according to... General Labourer Interested in getting paid weekly? If so, it’s all possible with this General Labourer job in St. Catharines, ON. Adecco is currently hiring for a temporary, part-time to full time General Labourer to work a n ongoing</p></div>","company":{"website":"adecco.ca","companyType":"Public/Established","name":"Adecco Canada","logoUrl":"/logos/adecco-a6e8d4caff6004eecbacd479e51def08.png"},"location":{"country":"Canada","address":"Grimsby, ON","city":"Grimsby","stateProvince":"ON"},"frontendLink":"/job-posting/adecco-canada/quality-assurance-associate/4287c8663a1fa492b8869c05fd625eff","title":"Quality Assurance Associate","hash":"4287c8663a1fa492b8869c05fd625eff","postingUrl":"https://ca.trabajo.org/job-649-20210503-927ca4783ac8fe4a680516d3adba8c2a"},{"employmentType":"Full-time","postedOn":"12 days ago","description":"<div><p>Aurora is a global leader in the cannabis industry serving both the medical and consumer markets. Headquartered in Edmonton, Alberta, Aurora is a pioneer in global cannabis dedicated to helping people improve their lives. The Company's brand portfolio includes Aurora, Aurora Drift, San Rafael '71, Daily Special, AltaVie, MedReleaf, CanniMed, Whistler, and Reliva CBD. Providing customers with innovative, high-quality cannabis products, Aurora's brands continue to break through as industry leaders in the medical, performance, wellness and recreational markets wherever they are launched. QUALITY ASSURANCE ASSOCIATE - WMMC Whistler Medical Marijuana Corp. a wholly owned subsidiary of Aurora Cannabis Inc. is currently recruiting for a Quality Assurance Associates to join our Pemberton and Whistler Facility, located in BC. The incumbent will report directly to the Manager, Quality Assurance this position will be responsible for the following: DUTIES: Represent QA as an ambassador for Cannabis Regulations, regulatory compliance with respect to GMP and company SOPs Implementation and continuous improvement of quality procedures Conduct training sessions for staff related to SOPs and general operational procedures (GMP/GPP). Perform Annual Product Review. Track metrics around compliance and efficiency and recommend measures to improve productivity and product quality. Participate in self inspection process. Conduct sanitation and pest control review to ensure compliance. Complete secondary batch review and all required follow up. CAPA review and approval, including documentation and investigation of non-conformances leading to identification of the root cause; Assigning and implementing an effective corrective and preventative action to promote continuous improvement. Responsible for compiling complaint summaries and necessary investigations. Responsible for quality assurance aspects of raw material control system. Work closely with production to ensure compliance is maintained. Assist manufacturing in drafting and writing SOPs that comply with the ACMPR and GMP. Participate in both internal and external audits as required. Assist VP Product Development and Quality Assurance as required in oversight of the facilities compliance. REQUIREMENTS 3-5 years' experience in the Quality Assurance Field Degree or diploma in a science related field Experience working in a regulated environment, pharmaceuticals, or natural health product manufacturing environment is preferred Understanding of Quality Management Systems including: batch record review, batch release, document control, change control, deviations, investigations and CAPA Fluency in MS Office is mandatory Competency of technological writing (SOPs, Annual Reports, Investigation Summary) Ability to work independently, with a strong attention to detail Ability to multitask and adapt to an evolving environment Ability to both speak and write clearly in English Whistler Medical Marijuana Corp. a wholly owned subsidiary of Aurora Cannabis Inc. is an Equal Opportunity Employer</p></div>","company":{"website":"auroramj.com","companyType":"Public/Established","name":"Aurora Cannabis","logoUrl":"/logos/aurora-cannabis-5846417b31dc1080e3c3b4583c3f2096.png"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/aurora-cannabis/quality-assurance-associate-wmmc/104cf6d86209f39c30597233d7b4a56e","title":"Quality Assurance Associate - WMMC","hash":"104cf6d86209f39c30597233d7b4a56e","postingUrl":"https://ca.trabajo.org/job-617-20210504-d307551b9405a1794410174d0c1e1b42"},{"postedOn":"11 hours ago","description":"<div><div><p><b>Who we are…</b></p><p>C3 Industries is led by a passionate, creative, and hardworking team of cannabis cultivation and processing experts. We produce and sell the highest quality, indoor cannabis flower and extracted products (<i>Cloud Cover Cannabis</i>) at our state-of-the-art facilities and retail storefronts (<i>High Profile Boutique Cannabis)</i> throughout Michigan and Oregon, with active expansion underway within Missouri and Massachusetts markets and communities.</p><p>At C3I our product is cannabis, but our most important asset is our people. We believe in hiring locally, offering competitive compensation packages, and giving our employees an opportunity to learn and grow. As a company, we are committed to being active corporate citizens and community members and celebrate diversity and inclusion.</p><p><b>We are looking for a Shift Lead</b><b> to join the new High Profile - Cape Girardeau team that can help guide patients through the process of understanding, selecting and acquiring cannabis products.</b></p><p><b>In this role you will….</b></p><ul><li>Provide the highest level of customer service by making the patient's experience the priority.</li><li>Assist patients to better understand product offerings and benefit.</li><li>Educate patients on cannabis properties and selection of proper genetics according to their desired effect, relief for patients' aliments or per request.</li><li>Serve as a role model for store employees in sales generation and customer service by making the customer experience the priority.</li><li>Handle customer complaints in a professional manner; handle escalated manners when Store Manager or Assistant Manager are not present.</li><li>Maintain product knowledge and keep up on current cannabis trends.</li><li>Accurately use and maintain Point of Sale (POS) system.</li><li>Comply with company cash handling policies and perform daily cash management responsibilities and compliance reporting per company policy.</li><li>Utilize down time productively to ensure sales floor is properly stocked for team members and next shift; Delegate and confirm team members are completing shift duties.</li><li>Open and close the store, assist with intake of product, inventory counts, and daily cash balancing.</li><li>Split tips, within company guidelines, among team members at the end of the business day when Store Manager is not present.</li><li>Contribute in management and store meetings, offering suggestions for employee development, sales opportunities, and organizational improvements.</li></ul><p><b>Skills and experience you have...</b></p><ul><li>3+ years' customer service experience, High school diploma or General Education Diploma (GED)</li><li>Experience opening and closing a retail store or restaurant preferred.</li><li>Experience with POS systems, and cash handling practices.</li><li>Commitment to reaching Key Performance Indicators on a regular basis.</li><li>Effective multi-tasker with demonstrated ability to prioritize tasks.</li><li>Ability to work independently with little or no direct supervision.</li><li>Demonstrate strong oral and written communication skills; ability to correspond in a professional and businesslike manner.</li><li>Knowledge of state and local regulations preferred.</li><li>Ability to pass a background check and is 21 years of age. Must obtain AGENT ID permit.</li></ul><p><b>You should apply if...</b></p><ul><li>You have an unwavering sense of accuracy with the ability to interpret ordinances and regulations.</li><li>You have a passion for the cannabis industry and are excited about working in a fast-paced start up.</li><li>You are detailed orientated and are comfortable doing whatever it takes to get the job done.</li></ul><div>Our mission is to share our love of cannabis with the world. If you're interested in being part of our journey, we'd love to hear from you!<br /><br /><ul><li><i>C3 Industries is not seeking to work with nor accepting resumes from recruitment or staffing agencies at this time. Thank you.</i></li></ul></div></div></div>","company":{"companyType":"Private/Established","name":"C3 Industries","logoUrl":"/logos/c3-industries-b10b21c6c8de56d113c9debefa664c78.png"},"location":{"country":"United States","address":"Cape Girardeau, MO","city":"Cape Girardeau","stateProvince":"MO"},"frontendLink":"/job-posting/c3-industries/retail-shift-lead/71830e7c0a43fdeee5f9fc9e48acd494","title":"Retail Shift Lead","hash":"71830e7c0a43fdeee5f9fc9e48acd494","postingUrl":"https://www.indeed.com/job/retail-shift-lead-0fe68e706a7bcb14"},{"employmentType":"Full-time","postedOn":"21 hours ago","description":"<div><p>Who we are…</p><p>C3 Industries is led by a passionate, creative, and hardworking team of cannabis cultivation and processing experts. We produce and sell the highest quality, indoor cannabis flower and extracted products (Cloud Cover Cannabis) at our state-of-the-art facilities and retail storefronts (High Profile Boutique Cannabis) throughout Michigan and Oregon, with active expansion underway within Missouri and Massachusetts markets and communities.</p><p>At C3I our product is cannabis, but our most important asset is our people. We believe in hiring locally, offering competitive compensation packages, and giving our employees an opportunity to learn and grow. As a company, we are committed to being active corporate citizens and community members and celebrate diversity and inclusion.</p><p>We are looking for a Shift Lead to join the new High Profile - Cape Girardeau team that can help guide patients through the process of understanding, selecting and acquiring cannabis products.</p><p>In this role you will….</p><p>• Provide the highest level of customer service by making the patient’s experience the priority.</p><p>• Assist patients to better understand product offerings and benefit.</p><p>• Educate patients on cannabis properties and selection of proper genetics according to their desired effect, relief for patients’ aliments or per request.</p><p>• Serve as a role model for store employees in sales generation and customer service by making the customer experience the priority.</p><p>• Handle customer complaints in a professional manner; handle escalated manners when Store Manager or Assistant Manager are not present.</p><p>• Maintain product knowledge and keep up on current cannabis trends.</p><p>• Accurately use and maintain Point of Sale (POS) system.</p><p>• Comply with company cash handling policies and perform daily cash management responsibilities and compliance reporting per company policy.</p><p>• Utilize down time productively to ensure sales floor is properly stocked for team members and next shift; Delegate and confirm team members are completing shift duties.</p><p>• Open and close the store, assist with intake of product, inventory counts, and daily cash balancing.</p><p>• Split tips, within company guidelines, among team members at the end of the business day when Store Manager is not present.</p><p>• Contribute in management and store meetings, offering suggestions for employee development, sales opportunities, and organizational improvements.</p><p><b>Skills and experience you have</b></p><p>• 3+ years’ customer service experience, High school diploma or General Education Diploma (GED)</p><p>• Experience opening and closing a retail store or restaurant preferred.</p><p>• Experience with POS systems, and cash handling practices.</p><p>• Commitment to reaching Key Performance Indicators on a regular basis.</p><p>• Effective multi-tasker with demonstrated ability to prioritize tasks.</p><p>• Ability to work independently with little or no direct supervision.</p><p>• Demonstrate strong oral and written communication skills; ability to correspond in a professional and businesslike manner.</p><p>• Knowledge of state and local regulations preferred.</p><p>• Ability to pass a background check and is 21 years of age. Must obtain AGENT ID permit.</p><p>You should apply if</p><p>• You have an unwavering sense of accuracy with the ability to interpret ordinances and regulations.</p><p>• You have a passion for the cannabis industry and are excited about working in a fast-paced start up.</p><p>• You are detailed orientated and are comfortable doing whatever it takes to get the job done.</p><p>Our mission is to share our love of cannabis with the world. If you’re interested in being part of our journey, we’d love to hear from you!</p><p>• C3 Industries is not seeking to work with nor accepting resumes from recruitment or staffing agencies at this time. Thank you.</p><p>By submitting your interest in this job, you agree to receive text notifications with additional steps to complete your job application. You will receive up to 6 messages from the number \"63879\". Message &amp; data rates may apply. Please refer to our privacy policy for more information</p></div>","company":{"companyType":"Public/Established","name":"High Profile Cannabis","logoUrl":"/logos/high-profile-cannabis-8ecd239c1004f093ff2525fccfc62cd1.jpeg"},"location":{"country":"United States","address":"Cape Girardeau, MO, USA","city":"Cape Girardeau","stateProvince":"MO"},"frontendLink":"/job-posting/high-profile-cannabis/retail-shift-lead/06695a6da0a12f844def809fb9a7b791","title":"Retail Shift Lead","hash":"06695a6da0a12f844def809fb9a7b791","postingUrl":"https://high-profile-cannabis-1.talentify.io/job/retail-shift-lead-cape-girardeau-missouri-high-profile-cannabis-89fbd5e7cf11-retail-shift-lead"},{"employmentType":"Full-time","postedOn":"2 days ago","description":"<div><p>Everyone is welcome here. Each of us is unique, and that's what makes us amazing. We believe in inclusiveness and celebrating each person's individuality, because there's power in bringing people with different points of view and life experiences together. That's why we provide equal employment opportunities (EEO). All applicants are considered regardless of race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, or sexual orientation. So, bring yourself and your best ideas; when we feel safe and comfortable being ourselves, there's no limit to what we can achieve. IN A NUTSHELL… The Lead Guide provides exceptional service and a high-quality experience for the Goodblend customers. In addition, the successful candidate must bring a positive presence, creating a collaborative work environment on the sales floor and provide excellent service to meet and exceed the stores financial goals. In addition, the Lead Guide will act as the stores Training Ambassador and assist with new employee, new launch and continued education and skill development of the team. Finally, the Lead Guide will assume the role of Manager on Duty as needed and be responsible for operational task follow through, opening, closing, banking and security of the store. This role is with Goodblend, one of the renowned retail brands under the Parallel umbrella. Parallel is one of the largest multi-state cannabis companies in the world, owning and operating in five markets; Florida (Surterra Wellness), Massachusetts (NETA), Pennsylvania (Goodblend), Nevada (The Apothecary Shoppe) and Texas (Surterra Wellness). If you enjoy companies that are growing, moving fast, and constantly challenging themselves to achieve more, then Parallel is for you. We work hard, lean on each other, and are passionate about a pretty ambitious vision … pioneering a new paradigm of what well-being can be for all people, everywhere. For more information, visit www.liveparallel.com. WHAT YOU WILL BE DOING Service * Prioritize time and energies in store to join the staff on the selling floor; coaching and developing the team; and leading by example. * Positive representative of the Goodblend brand delivering the full Goodblend customer service experience, catering to the customers' needs. * Work in collaboration with Manager to enhance company culture by celebrating training successes and encouraging continued education through positive reinforcement and team building. * Develops knowledge of trends in industry to provide the best service possible and share with the team. * Responds to all customer concerns and acts when necessary to resolve conflicts. * Serves as a role-model and resource for store staff concerning products and services, policies and procedures, industry news, and changes in regulations. Operations * Fulfill Manager on Duty responsibilities, including all opening and closing responsibilities, banking responsibilities, managing down time to be productive, maintaining cleanliness standards * Must adhere to all company policies and procedures. Immediately report any variances to a Manager or the HR team. * Maintain knowledge of all applicable state and local laws, as well as documentation processes in accordance with the State of Pennsylvania. * Maintain caregiver paperwork in accordance with the State of Pennsylvania, maintain tracking in system and communicating changes to physicians. * Completes opening and closing responsibilities accurately and efficiently and ensures cash handling standards are met and company funds are secured. * Assists in execution of visual displays, merchandising and marketing standards ensuring the store is consistently replenished. * Assists in the preparation and completion of accurate physical inventory as assigned. * Assists with non-sell tasks as assigned by Management and as part of the daily responsibilities. * Use the POS accurately and train all Guides on POS in addition to other operational tasks. * Arrives to work on time and consistently follows the Goodblend personal appearance guidelines. * Follows all safety and emergency procedures. * Perform additional duties as assigned. Leadership * Contributes to a productive and dynamic environment by connecting with employees, customers, and the community. * Acts with professionalism and respect in all interactions with customers, co-workers, Manager and team, and always ensuring customer service standards are met and prioritized and the sales floor is a welcoming environment. Education * Closely monitor, educate, and coach all new team members during their first two weeks. * Provide coaching and education to all team members on product and cannabis knowledge. * Provide training to ensure all store processes align with SOP's and safe practices. * Collaborate with Managers to evaluate and review strengths and opportunities for new and existing team members. Assist Managers in developing a plan to improve performance. * Provide information to Manager regarding team completion of assigned GZ courses. * Provide feedback to Training Team and make recommendations for future development and/or current program improvement. EXPERIENCE AND SKILLS YOU'LL BRING * 2 years retail experience, previous sales experience (Required) * Excellent customer service, communication and organizational skills * Ability to multi-task and build relationships * Flexibility and the ability to handle change in a positive manner * Demonstrated ability to support business growth and exhibit professional behavior * Have and maintain flexible availability * Must have open flexibility to work during peak traffic times including evenings, weekends and holidays * Age 21 or over (Required) * High School Diploma or equivalent (Required) * Valid Government-Issued Photo ID (Required) YOU WILL BE SUCCESSFUL IF YOU… * Are self-motivated; micro-managing isn't fun for anyone * Roll your sleeves up and do the work; strategy is important, but so is getting stuff done * Can work fast and be flexible; our industry is always changing * Play nice with others; we collaborate with each other a lot * Think creatively; sometimes, the \"traditional\" solution isn't the best one WHAT YOU GET * Consistent, reliable benefits; Full medical/vision/dental, 401k with a possible company match, access to company-sponsored well-being programs * Balance and flexibility; paid time off, paid parental leave, flexible work arrangements * Financial opportunity; an incentive program that provides opportunity to earn cash AND equity in a fast-growing company and industry * Employee discount * Chance to make a difference; Employee Relief Fund, community volunteerism opportunities through Benevity PHYSICAL REQUIREMENTS * Able to lift, push and pull up to 50 pounds * Able to stand on your feet for up to 8 hours PARALLEL IS UNITED BY OUR VISION, MISSION, &amp; VALUES Our Vision - why we exist - is to pioneer well-being and improve the quality of life for humanity through the benefits of cannabinoids. Our Mission - how we will do this - is to build a leading, global well-being company through the best talent, our values, trusted and recognized brands, science and technology-based innovation, and a relentless focus on execution and continuous improvement. Our Values - Integrity | Collaboration | Alignment | Intentionality | Accountability | Agility We are an Equal Opportunity Employer. We embrace and encourage our employees' differences in age, color, disability, ethnicity, gender identity or expression, language, national origin, physical and mental ability, political affiliation, race, religion, sexual orientation, socioeconomic status, veteran status, and other characteristics that make our employees unique</p></div>","company":{"companyType":"Private/Established","name":"Surterra Holdings","logoUrl":"/logos/surterra-holdings-36438f9065d6c02f268a36670ac6dcfa.jpeg"},"location":{"country":"United States","address":"Erie, PA, USA","city":"Erie","stateProvince":"PA"},"frontendLink":"/job-posting/surterra-holdings/lead-guide-retail/a160f58b228a0c27fbaafcd5419f4ee8","title":"Lead Guide - Retail","hash":"a160f58b228a0c27fbaafcd5419f4ee8","postingUrl":"https://us.trabajo.org/job-640-20210513-a22f4949416afac77e4a216b7ddbe07d"},{"employmentType":"Full-time","postedOn":"2 days ago","description":"<div><p>Who we are…</p><p>C3 Industries is led by a passionate, creative, and hardworking team of cannabis cultivation and processing experts. We produce and sell the highest quality, indoor cannabis flower and extracted products (Cloud Cover Cannabis) at our state-of-the-art facilities and retail storefronts (High Profile Boutique Cannabis) throughout Michigan and Oregon, with active expansion underway within Missouri and Massachusetts markets and communities.</p><p>At C3I our product is cannabis, but our most important asset is our people. We believe in hiring locally, offering competitive compensation packages, and giving our employees an opportunity to learn and grow. As a company, we are committed to being active corporate citizens and community members and celebrate diversity and inclusion.</p><p>We are looking for a Shift Lead to join the new High Profile - Kalamazoo team that can help guide patients through the process of understanding, selecting and acquiring cannabis products.</p><p>In this role you will….</p><p>• Provide the highest level of customer service by making the patient’s experience the priority.</p><p>• Assist patients to better understand product offerings and benefit.</p><p>• Educate patients on cannabis properties and selection of proper genetics according to their desired effect, relief for patients’ aliments or per request.</p><p>• Serve as a role model for store employees in sales generation and customer service by making the customer experience the priority.</p><p>• Handle customer complaints in a professional manner; handle escalated manners when Store Manager or Assistant Manager are not present.</p><p>• Maintain product knowledge and keep up on current cannabis trends.</p><p>• Accurately use and maintain Point of Sale (POS) system.</p><p>• Comply with company cash handling policies and perform daily cash management responsibilities and compliance reporting per company policy.</p><p>• Utilize down time productively to ensure sales floor is properly stocked for team members and next shift; Delegate and confirm team members are completing shift duties.</p><p>• Open and close the store, assist with intake of product, inventory counts, and daily cash balancing.</p><p>• Split tips, within company guidelines, among team members at the end of the business day when Store Manager is not present.</p><p>• Contribute in management and store meetings, offering suggestions for employee development, sales opportunities, and organizational improvements.</p><p><b>Skills and experience you have</b></p><p>• 3+ years’ customer service experience, High school diploma or General Education Diploma (GED)</p><p>• Experience opening and closing a retail store or restaurant preferred.</p><p>• Experience with POS systems, and cash handling practices.</p><p>• Commitment to reaching Key Performance Indicators on a regular basis.</p><p>• Effective multi-tasker with demonstrated ability to prioritize tasks.</p><p>• Ability to work independently with little or no direct supervision.</p><p>• Demonstrate strong oral and written communication skills; ability to correspond in a professional and businesslike manner.</p><p>• Knowledge of state and local regulations preferred.</p><p>• Ability to pass a background check and is 21 years of age.</p><p>You should apply if</p><p>• You have an unwavering sense of accuracy with the ability to interpret ordinances and regulations.</p><p>• You have a passion for the cannabis industry and are excited about working in a fast-paced start up.</p><p>• You are detailed orientated and are comfortable doing whatever it takes to get the job done.</p><p>Our mission is to share our love of cannabis with the world. If you’re interested in being part of our journey, we’d love to hear from you!</p><p>• C3 Industries is not seeking to work with nor accepting resumes from recruitment or staffing agencies at this time. Thank you.</p><p>By submitting your interest in this job, you agree to receive text notifications with additional steps to complete your job application. You will receive up to 6 messages from the number \"63879\". Message &amp; data rates may apply. Please refer to our privacy policy for more information</p></div>","company":{"companyType":"Public/Established","name":"High Profile Cannabis","logoUrl":"/logos/high-profile-cannabis-8ecd239c1004f093ff2525fccfc62cd1.jpeg"},"location":{"country":"United States","address":"Kalamazoo, MI, USA","city":"Kalamazoo","stateProvince":"MI"},"frontendLink":"/job-posting/high-profile-cannabis/retail-shift-lead/b474952b0c9500b26bc8988381869fcb","title":"Retail Shift Lead","hash":"b474952b0c9500b26bc8988381869fcb","postingUrl":"https://high-profile-cannabis-1.talentify.io/job/retail-shift-lead-kalamazoo-michigan-high-profile-cannabis-4cbea5f60c82-retail-shift-lead"},{"postedOn":"10 hours ago","description":"<div><div><div><h2><b>Duties</b></h2><h3><b>Summary</b></h3><div><p>You will serve as an Electrical Engineer in the Facility Management and Sustainment Division of the Facilities, Maintenance &amp; Logistics Management Department at Naval Computer and Telecommunications Area Master Station, Pacific of (NCTAMS PACIFIC).</p><br /></div><h3><b>Responsibilities</b></h3><div><ul><li>You will provide electrical guidance and oversee the balancing of power during the planning, installation, modification or renovation phases.</li><li>You will provide consultation to NCTAMS PAC and subordinate activities within the Pacific Region AOR to resolve difficult issues/problems related to power, air conditioning, facilities and high-altitude electromagnetic pulse (HEMP) protection.</li><li>You will provide input on command publications, instruction guidance/criteria and will be the focal point/advisor for the issues, interpretation of facilities regulations and problems that cannot be resolved at the local level.</li><li>You will be responsible for Electrical Power Plant property and accounting of all NCTAMS PAC owned Class II assets.</li><li>You will be responsible for branch correspondence, memoranda and other reports required by higher officials, other tenants and commands related to the maintenance, repair and alteration of all NCTAMS facilities.</li><li>You will initiate work requests, monitor progress, engineering and architectural service request, status reports on all activity projects, prepare funding justifications, assemble data and backup information to support correspondence responses.</li></ul></div><div><h3><b>Travel Required</b></h3><p>Occasional travel - You may be expected to travel for this position.</p></div><div><div><h5><b>Supervisory status</b></h5><p>No</p></div><div><h5><b>Promotion Potential</b></h5><p>13</p></div></div></div><ul><li><div><h4><b>Job family (Series)</b></h4><p>0850 Electrical Engineering</p><div><h4><b>Similar jobs</b></h4><ul><li>Electrical And Electronics Engineers</li><li>Electrical Engineers</li><li>Electrical Systems Engineers</li><li>Engineers, Electrical</li><li>Engineers, Electrical Systems</li><li>Engineers, Power Distribution</li></ul></div></div></li></ul><ul><li><p>Requirements</p><div><h2><b>Requirements</b></h2><h3><b>Conditions of Employment</b></h3><ul><li>This is a Sensitive Compartmented Information (SCI) position.</li><li>Must be a US Citizen.</li><li>Must be determined suitable for federal employment.</li><li>Must participate in the direct deposit pay program.</li><li>New employees to the Department of the Navy will be required to successfully pass the E-Verify employment verification check. To learn more about E-Verify, including your rights and responsibilities, visit e-verify.gov</li><li>Within the Department of Defense (DoD), the appointment of retired military members within 180 days immediately following retirement date to a civilian position is subject to the provisions of 5 United States Code 3326.</li><li>Males born after 12-31-59 must be registered for Selective Service.</li><li>You will be required to obtain and maintain an Top Secret SCI interim and/or final security clearance prior to entrance on duty. Failure to obtain and maintain the required level of clearance may result in the withdrawal of a job offer or removal.</li><li>Successful completion of a pre-employment drug test (including marijuana) is required. A tentative offer of employment will be rescinded if you fail to report to the drug test appointment or pass the test. You will be subject to random testing.</li><li>You will be required to obtain and maintain a valid driver's license.</li><li>You are subject to a polygraph examination.</li><li>You will be required to perform some travel away from the normal duty station.</li></ul><div><h3><b>Qualifications</b></h3><div>Applicants must meet the following B<b>asic Education</b> requirements of the Office of Personnel Management (OPM) Qualifications Standards Manual:<br /><br />Successful completion of a professional engineering degree. To be acceptable, the program must: (1) lead to a bachelor's degree in a school of engineering with at least one program accredited by ABET; or (2) include differential and integral calculus and courses (more advanced than first-year physics and chemistry) in five of the following seven areas of engineering science or physics: (a) statics, dynamics; (b) strength of materials (stress-strain relationships); (c) fluid mechanics, hydraulics; (d) thermodynamics; (e) electrical fields and circuits; (f) nature and properties of materials (relating particle and aggregate structure to properties); and (g) any other comparable area of fundamental engineering science or physics, such as optics, heat transfer, soil mechanics, or electronics<br /><br /><b>OR</b><br /><br />Combination of education and experience - college-level education, training, and/or technical experience that furnished (1) a thorough knowledge of the physical and mathematical sciences underlying engineering, and (2) a good understanding, both theoretical and practical, of the engineering sciences and techniques and their applications to one of the branches of engineering. The adequacy of such background must be demonstrated by one of the following:<br /><br />1. Professional registration or licensure - Current registration as an Engineer Intern (EI), Engineer in Training (EIT)1, or licensure as a Professional Engineer (PE) by any State, the District of Columbia, Guam, or Puerto Rico. Absent other means of qualifying under this standard, those applicants who achieved such registration by means other than written test (e.g., State grandfather or eminence provisions) are eligible only for positions that are within or closely related to the specialty field of their registration. For example, an applicant who attains registration through a State Board's eminence provision as a manufacturing engineer typically would be rated eligible only for manufacturing engineering positions.<br />2. Written Test - Evidence of having successfully passed the Fundamentals of Engineering (FE)2 examination or any other written test required for professional registration by an engineering licensure board in the various States, the District of Columbia, Guam, and Puerto Rico.<br />3. Specified academic courses - Successful completion of at least 60 semester hours of courses in the physical, mathematical, and engineering sciences and that included the courses specified in the basic requirements under paragraph A. The courses must be fully acceptable toward meeting the requirements of an engineering program as described in paragraph A.<br />4. Related curriculum - Successful completion of a curriculum leading to a bachelor's degree in an appropriate scientific field, e.g., engineering technology, physics, chemistry, architecture, computer science, mathematics, hydrology, or geology, may be accepted in lieu of a bachelor's degree in engineering, provided the applicant has had at least 1 year of professional engineering experience acquired under professional engineering supervision and guidance. Ordinarily there should be either an established plan of intensive training to develop professional engineering competence, or several years of prior professional engineering-type experience, e.g., in interdisciplinary positions. (The above examples of related curricula are not all-inclusive.)<br /><br /><b>In addition to the Basic Education Requirements for this position, you must have directly applicable experience that demonstrates the possession of knowledge, skills, abilities, and competencies necessary for immediate success in the position.</b> Qualifying experience may have been acquired in any public or private sector job, but will clearly demonstrate past experience in the application of the particular competencies or knowledge, skills and abilities necessary to successfully perform the duties of the position. Such experience is typically in or directly relates to the work of the position to be filled.<b> Qualifying experience would be demonstrated by:</b><br /><br />Working with Communications Stations and Data Center Planning, design, construction and maintenance;<br /><br />Utilizing electrical power engineering, operations and maintenance of emergency generators, uninterruptible power supplies (UPS), breakers and related control systems to plan work;<br /><br />Utilizing advance techniques of electrical engineering in requirements for complex electrical distribution systems serving Communications Stations and Data Centers;<br /><br />Budgeting, programming and acquisitions using annual funds for the operation and maintenance of electrical power systems;<br /><br />Formulating and development of supporting documentation, in order to plan and program repair, construction, site preparation projects involving the electrical distribution system, emergency generators, UPS. Antennas and Communications-Electronic (C-E) system installations.<br /><br />This position is within the Work Category Professional at Work Level Senior III, GG-0850-13.<br /><br />https://www.opm.gov/policy-data-oversight/classification-qualifications/general-schedule-qualification-standards/0800/electrical-engineering-series-0850/<br /><br />Additional qualifications information can be found from the following Department of Defense website: https://dodcio.defense.gov/Cyber-Workforce/CES.aspx</div></div><div><h3><b>Education</b></h3><p>Applicants must meet the following B<b>asic Education</b> requirements of the Office of Personnel Management (OPM) Qualifications Standards Manual:<br /><br />Successful completion of a professional engineering degree. To be acceptable, the program must: (1) lead to a bachelor's degree in a school of engineering with at least one program accredited by ABET; or (2) include differential and integral calculus and courses (more advanced than first-year physics and chemistry) in five of the following seven areas of engineering science or physics: (a) statics, dynamics; (b) strength of materials (stress-strain relationships); (c) fluid mechanics, hydraulics; (d) thermodynamics; (e) electrical fields and circuits; (f) nature and properties of materials (relating particle and aggregate structure to properties); and (g) any other comparable area of fundamental engineering science or physics, such as optics, heat transfer, soil mechanics, or electronics<br /><br /><b>OR</b><br /><br />Combination of education and experience - college-level education, training, and/or technical experience that furnished (1) a thorough knowledge of the physical and mathematical sciences underlying engineering, and (2) a good understanding, both theoretical and practical, of the engineering sciences and techniques and their applications to one of the branches of engineering. The adequacy of such background must be demonstrated by one of the following:<br /><br />1. Professional registration or licensure - Current registration as an Engineer Intern (EI), Engineer in Training (EIT)1, or licensure as a Professional Engineer (PE) by any State, the District of Columbia, Guam, or Puerto Rico. Absent other means of qualifying under this standard, those applicants who achieved such registration by means other than written test (e.g., State grandfather or eminence provisions) are eligible only for positions that are within or closely related to the specialty field of their registration. For example, an applicant who attains registration through a State Board's eminence provision as a manufacturing engineer typically would be rated eligible only for manufacturing engineering positions.<br />2. Written Test - Evidence of having successfully passed the Fundamentals of Engineering (FE)2 examination or any other written test required for professional registration by an engineering licensure board in the various States, the District of Columbia, Guam, and Puerto Rico.<br />3. Specified academic courses - Successful completion of at least 60 semester hours of courses in the physical, mathematical, and engineering sciences and that included the courses specified in the basic requirements under paragraph A. The courses must be fully acceptable toward meeting the requirements of an engineering program as described in paragraph A.<br />4. Related curriculum - Successful completion of a curriculum leading to a bachelor's degree in an appropriate scientific field, e.g., engineering technology, physics, chemistry, architecture, computer science, mathematics, hydrology, or geology, may be accepted in lieu of a bachelor's degree in engineering, provided the applicant has had at least 1 year of professional engineering experience acquired under professional engineering supervision and guidance. Ordinarily there should be either an established plan of intensive training to develop professional engineering competence, or several years of prior professional engineering-type experience, e.g., in interdisciplinary positions. (The above examples of related curricula are not all-inclusive.)<br /><br />Note: An applicant who meets the basic requirements as specified in A or B above, except as noted under B.1., may qualify for positions in any branch of engineering unless selective factors indicate otherwise.</p></div><div><h3><b>Additional information</b></h3><div><p>This position is a DoD Cyber Excepted Service (CES) personnel system position in the Excepted Service under 10 U.S.C. 1599f.<br /><br />Additional vacancies may be filled by this announcement.<br /><br />Recruitment incentives may be authorized to eligible new hires.<br /><br />A relocation incentive is generally a single payment intended to offset some of the relocation costs experienced by the selectee. A relocation incentive may be authorized.<br /><br />A tentative offer of employment will be rescinded if the selectee fails to meet the pre-employment requirements, including failure to report to any of the scheduled appointments.<br /><br />If you are unable to apply online and request information about the Alternate Application process, please contact the Department of Navy's Employment Information Center.<br /><br />Federal annuitant information: The selection of an annuitant is subject to the Department of Defense and Department of the Navy policy on the employment of annuitants. Policy information may be found at: http://www.secnav.navy.mil/donhr/Documents/CivilianJobs/FedCivAnnuitants.pdf<br /><br />The Cyber Interagency Transfer Authority (CITA) permits movement of CES employees appointed under Section 1599f of Title 10 U.S.C. and excepted service employees appointed under Schedule A, Section 213.3106(b)(11) of Title 5 CFR, info cyber workforce positions in the competitive service and movement of competitive service employees into DoD Cyber Workforce positions within the Military Departments and Defense Agencies.<br /><br />This position is in the excepted service and does not confer competitive status.<br /><br />DoD Components with CES positions apply Veterans' Preference to preference eligible candidates as defined by Section 2108 of Title 5 U.S.C., in accordance with the procedures provided in DoD Instruction 1400.25, Volume 3005, \"CES Employment and Placement.\" If you are a veteran claiming veterans' preference, as defined by Section 2108 of Title 5 U.S.C., you must submit documents verifying your eligibility with your application package.</p><br /></div></div><div><h3><b>How You Will Be Evaluated</b></h3><div><p>You will be evaluated for this job based on how well you meet the qualifications above.</p><p>In order to qualify for this position, your resume must be provided sufficient experience and/or education, knowledge, skills, and abilities to perform the duties of the specific position for which you are being considered. Your resume is the key means we have for evaluating your skills, knowledge, and abilities as they relate to this position. Therefore, we encourage you to be clear and specific when describing your experience.<br /><br />When the application process is complete, we will review your resume to ensure you meet the hiring eligibility and qualification requirements listed in this announcement. You will be rated based on the information provided in your resume and responses to the Occupational Questionnaire, along with your supporting documentation to determine your ability.<br /><br />If selected, you may be required to provide supporting documentation.<br /><br />If after reviewing your resume and supporting documentation, a determination is made that you inflated your qualifications and/or experience, your score may be adjusted to more accurately reflect your abilities or you may be found ineligible/not qualified.<br /><br />Please follow all instructions carefully. Errors or omissions may be affect your rating or consideration for employment.<br /><br />All qualifications requirements must be met by the closing date of this announcement.<br /><br />Experience refers to paid and unpaid experience, including volunteer work done through National Service programs (e.g., professional, philanthropic, religious, spiritual, community, student, social). Volunteer work helps build critical competencies, knowledge, and skills and can provide valuable training and experience that translates directly to paid employment.<br /></p></div><p></p><div><h3><b>Background checks and security clearance</b></h3><div><div><h5><b>Security clearance</b></h5><p>Sensitive Compartmented Information</p></div><div><h5><b>Drug test required</b></h5><p>Yes</p></div></div><div><div><h5><b>Position sensitivity and risk</b></h5><p>Special-Sensitive (SS)/High Risk</p></div><div><h5><b>Trust determination process</b></h5><p>National security</p></div></div></div></div></div></li></ul><ul><li><p>Required Documents</p><div><h2><b>Required Documents</b></h2><div><p><b>You are required to provide documentation that supports the eligibility and qualification claims made in your resume and assessment questionnaire</b>. You must submit the applicable documents listed here and those listed with the eligibilities you select in the announcement questionnaire with your application package. Applicants who do not provide supporting documentation that fully support their claims will not be referred to the hiring manager. Cover letter is optional. <b>A complete resume is required.</b> Your resume must show relevant experience, job title, duties and accomplishments. Your resume must show complete information for each job entry to support minimum qualifications. The following information should be provided in your resume, but it is acceptable to provide elsewhere in your application package: employer's name, starting and end dates (Mo/Yr), hours per week, and pay plan, series and grade level (e.g. GS-0201-09) for relevant federal experience.TIP: A good way to ensure you include all essential information is to use the Resume Builder in USAJOBS to create your resume.<br /><br /><b>Are you claiming membership in any professional organizations, or possession of a license, certificate or credentials? </b>Check the <b>Conditions of Employment </b>section above to see if any are required. If you claim membership, license, certification, or credentials, you must submit a copy of said document in your application package.<br /><br /><b>Are you using education as a substitute for some or all of the experience requirement? Is there a basic education requirement for this position?</b> Check the <b>Education</b> section above to see what is allowed and what is required. Any claims you make in your resume or assessment questionnaire regarding education or degrees MUST be supported by submitting with your application official or unofficial transcripts or a list of courses, grades earned, completion dates, and quarter and semester hours earned issued from your school. While unofficial transcripts are acceptable for initial application, an official transcript will ultimately be required if you are selected for the position. You may submit a copy your degree(s) if specific coursework does not have to be verified.<br /><br /><b>Are you a veteran claiming 5-point veterans' preference</b> or <b>claiming sole survivorship preference? </b>You must submit a copy of your latest DD-214 Certificate of Release or Discharge from Active Duty (any copy that shows all dates of service, as well as character of service [Honorable, General, etc.] is acceptable) OR a VA letter that shows dates of service or service connected disability AND character of service. If you have more than one DD-214 for multiple periods of active duty service, submit a copy for each period of service. If you were issued a DD-215 to amend aforementioned information on the DD-214 you must submit that too. If you are not sure of your preference eligibility, visit the Department of Labor's website: Veterans' Preference Advisor<br /><br /><b>Are you a disabled veteran or claiming 10-point veterans' preference?</b><br />If you are eligible to claim 10 point veterans preference you must submit a DD-214 Certificate of Release or Discharge from Active Duty as described above for 5-point preference.<br /><br />You must also provide the applicable supporting documentation of your disability (e.g. disability letter from the VA) as described on Standard Form-15 (SF-15). http://www.opm.gov/forms/pdf_fill/SF15.pdf.<br /><br /><b>Are you an active duty service member?</b> Active Duty Service Members are required to submit a statement of service printed on command letterhead and signed by the command. The statement of service must provide the branch of service, rate/rank, all dates of service, the expected date of discharge and anticipated character of service (Honorable, General, etc.).<br /><br />Documents submitted as part of the application package, to include supplemental documents, may be shared beyond the Human Resources Office. Some supplemental documents contain personal information such as SSN and DOB and some documents such as military orders and marriage certificates may contain personal information for someone other than you. You may sanitize these documents to remove said personal information before you submit your application. You must provide an un-sanitized version of the documents if you are selected.</p><div><h4><b>If you are relying on your education to meet qualification requirements:</b></h4><p>Education must be accredited by an accrediting institution recognized by the U.S. Department of Education in order for it to be credited towards qualifications. Therefore, provide only the attendance and/or degrees from schools accredited by accrediting institutions recognized by the U.S. Department of Education.</p><p>Failure to provide all of the required information as stated in this vacancy announcement may result in an ineligible rating or may affect the overall rating.</p></div></div></div></li></ul><ul><li><p>Benefits</p><div><h2><b>Benefits</b></h2><div><p>A career with the U.S. Government provides employees with a comprehensive benefits package. As a federal employee, you and your family will have access to a range of benefits that are designed to make your federal career very rewarding. Opens in a new windowLearn more about federal benefits.</p><p></p><p>Review our benefits</p><div><p>Eligibility for benefits depends on the type of position you hold and whether your position is full-time, part-time, or intermittent. Contact the hiring agency for more information on the specific benefits offered.</p></div></div></div></li></ul></div><p></p><br /><div>Help<h3><b>This job is open to</b></h3><ul><li><div><h4><b>The public</b></h4><p>U.S. citizens, nationals or those who owe allegiance to the U.S.</p></div></li></ul><div><h4><b>Clarification from the agency</b></h4><p>U.S. Citizens</p></div></div></div>","company":{"companyType":"Government","name":"US United States Fleet Forces Command","logoUrl":"/logos/us-united-states-fleet-forces-command-13ace0a83b45c204eb1e9d3bc5d5ff7c.png"},"location":{"country":"United States","address":"Wahiawā, HI","city":"Wahiawā","stateProvince":"HI"},"frontendLink":"/job-posting/us-united-states-fleet-forces-command/electrical-engineer/53dc7326b6b65228f6b3d24490f302f3","title":"ELECTRICAL ENGINEER","hash":"53dc7326b6b65228f6b3d24490f302f3","postingUrl":"https://www.indeed.com/job/electrical-engineer-bed6fd278bf56d19"},{"employmentType":"Full-time","postedOn":"10 hours ago","description":"<div><p><b><i>The Company </i></b></p><p>Isolate Extraction Systems Inc. (IES) designs, manufactures and services safe, high quality, food-grade super-critical CO2 extraction machines backed by deep expertise and customer satisfaction. A recognized market leader in botanical and hemp/cannabis extraction, we continue to develop state of the art technology and procedures to manufacture the most advanced equipment with a focus on safety, efficiency, reliability, and ease of use. Our extractors are 100% automated using proprietary in-house designed software and built in the USA. We are committed to ensuring our customers’ long-term success through ongoing relationships and continuous improvements. Founded in 2012, IES has recently expanded to Upstate NY to be part of the P1 Ventures private equity firm.</p><p><b><i>Role &amp; Responsibilities </i></b></p><p>IES is looking for a motivated and collaborative manufacturing engineer to add to our engineering team. This role will work closely with the engineering and production teams to develop and optimize production processes and documentation, be actively involved with drawings and revisions, and assist with new product development of prototypes into production models. With a focus on Lean Manufacturing, the manufacturing engineer will work with the team to standardize and continuously improve production processes. The person in this role will also have the opportunity to be part of setting up new production facility sites. This role will primarily be based in Lousiville, CO, with some travel to our production plant in Upstate NY.</p><p><i>Duties include but are not limited to: </i></p><ul><li>Implement production process improvements to existing and future product lines</li></ul><ul><li>Facilitate transition of R&amp;D prototypes units to full-scale production models</li></ul><ul><li>Measure production cell performance and cycle times</li></ul><ul><li>Implement and maintain ECO and deviation documentation</li></ul><ul><li>Management of product line CAD models and manufacturing blueprints</li></ul><ul><li>Create Standard Work Instruction for production employees</li></ul><ul><li>Maintaining revision control throughout multiple parts, sub-assemblies, and complex assemblies.</li></ul><ul><li>Maintain vendor supplied drawings and manage submittal packages</li></ul><ul><li>Develop tools to standardize complex assemblies in a production environment</li></ul><ul><li>Assist in setting up new production facility sites</li></ul><ul><li>Provide weekly progress reports to management</li></ul><p><i>Qualifications </i></p><ul><li>Bachelor’s degree in engineering</li></ul><ul><li>5+ years of engineering experience</li></ul><ul><li>Ability to travel 25-50% of the time</li></ul><ul><li>Strong AutoCAD Inventor skills</li></ul><ul><li>Extreme attention to detail</li></ul><ul><li>Strong GD&amp;T knowledge base</li></ul><ul><li>Confidence and ability to communicate your ideas clearly to fellow employees</li></ul><ul><li>Strong understanding of mechanical assemblies and fabrication</li></ul><ul><li>Strong communication and organizational skills</li></ul><ul><li>Intermediate or advanced MS Office (Excel, Word, Outlook)</li></ul><ul><li>Ability to manage multiple tasks and priorities with frequent interruptions</li></ul><ul><li>Ability to work effectively and efficiently with internal customers and company personnel with diverse backgrounds and abilities</li></ul><ul><li>Self-motivated to continuously improve</li></ul><p>Job Type: Full-time</p><p>Pay: $70,000.00 - $85,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li></ul><p>Schedule:</p><ul><li>Monday to Friday</li></ul><p>Education:</p><ul><li>Bachelor's (Required)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Isolate Extraction Systems","logoUrl":"/logos/isolate-extraction-systems-80275a8ea106e7a3914f5b60d0e64b3e.png"},"location":{"country":"United States","address":"Louisville, CO 80027","city":"Louisville","stateProvince":"CO"},"frontendLink":"/job-posting/isolate-extraction-systems/manufacturing-engineer/d01db235fa6b183617d39434e3a5530f","title":"Manufacturing Engineer","hash":"d01db235fa6b183617d39434e3a5530f","postingUrl":"https://www.indeed.com/job/manufacturing-engineer-162559f013f990c3"}]