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Quality Engineer

iAnthus Capital Holliston, MA, USA $67k - $110k - Full-time
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Mayflower Medicinals, Inc (MMI) is part of a larger, well-capitalized network of companies brought together to support best-in-class licensed cannabis cultivators, processors and dispensaries throughout the United States. We are a patient first focused organization providing top quality medical cannabis in a compassionate, warm environment. We aim to be an employer of choice and as such offer a robust compensation package including competitive salary, full medical benefits, and employee discounts!

Summary

The Quality Engineer I is a technical professional position, reporting to the Quality Manager. The Quality Engineer will be focused on defining, measuring, improving and maintaining product quality through improvements in our production processes, equipment and employee skills. In this regard, they will be the subject matter expert and authority at their site or region on all matters that are quality related.

A qualified candidate will be analytical, have extensive cross-functional experience, is a seasoned operator, influencer, and collaborator, and will have a track record of operating within a mature manufacturing system.

Essential Responsibilities

• Work with the Manager to define quality metrics: specific, measurable and relevant.

• Establish quality control points -- throughout the cultivation and processing system -- for the above metrics

• Lead a cross functional team to identify quality improving projects and then drive the top projects to deliver results

• Evaluate proposed process or equipment changes for potential impact on quality

• Be the site’s or region’s subject matter expert on quality control and assurance

• Work with Manager to develop and/or enhance manufacturing processes and controls and the capturing of quality control data.

• Work with the Manager to select and implement a software-based platform for capturing and dashboarding quality control metrics. This may include but is not limited to developing within the ERP, the data capturing methods and tools necessary to report status upwards. As needed, this will include the deployment of data capturing sensors and test equipment.

• Drive the investigation of out-of-control processes, identify root cause and implement improvements to significantly reduce the frequency and/or impact of future occurrences

• As needed, provide due diligence support with respect to any acquisition of a new operation. This would include but not be limited to the evaluation of the scope and span of quality systems.

• Keep informed of the best quality practices within and without iAnthus and drive the adoption of them

• Establish a cadence for communicating in a timely and concise way the status of metrics, projects, issues, etc.

• Ensure a safe work environment and a culture that embraces safe work habits, understanding of the risks, compliance with regulations, and prioritizing corrective action of any identified safety hazards or risks

• Ensure Team Members have the tools, knowledge, and equipment required to do their jobs

• Ensure that the Quality systems, testing and compliance of all company products facilitates brand leadership and exceeds legal requirements and leads to delighted customers.

Education and Skills Requirements

• Must be at least 21 years old

• A bachelor’s degree in Engineering or Science with appropriate training in manufacturing and quality control methods preferred.

• An exception to the B.S. degree will be considered when a candidate presents a great attitude and aptitude to learn analytical skills that are common to quality professionals (e.g., basic statistics, SPC, spreadsheet usage, experiment design, etc.)

• Green belt certification in Lean Manufacturing or a basic introductory course and equivalent experience

• Minimum of 2 years of industrial experience where quality was part of the culture

• Minimum of 2 years’ experience as a team leader or Supervisor

• Project management experience which includes being proficient with project management tools such as Microsoft Project.

• An effective and persuasive communicator that constantly strives for simplicity and clarity.

Physical and Environmental Requirements

• Ability to work a minimum of 10 hours a day and rotating shifts;

• Flexible schedule availability including nights, weekends and holidays;

• Ability to lift, push, and pull 50 pounds;

• Ability to sit, squat, bend, and kneel repetitively throughout a work day;

• Ability to stand for extended periods of time;

• Ability to use a ladder (up to 12 ft. extension) and general hardware tools needed for common repairs;

• Ability and willingness to work in the following conditions:

• General office environment;

• Extended computer usage;

• Extended phone usage including teleconferences, and

• Work environments that include exposure to, but not limited to, fumes, dust, odors, heights, indoor AC, no AC, motion, and noise.

MMI encourages applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. MMI believes in creating and sustaining a robust policy of inclusivity and diversity. MMI recognizes that diversity in the workforce is key to the integrity of a company’s commitment to its community. MMI’s Diversity & Inclusion Plan is designed to promote equity among minorities, women, veterans, people with disabilities, and people who identify as LGBTQ+. MMI will make every effort to employ and advance in employment qualified and diverse people at all levels within the company.

We value all team members by embracing their diverse talents, perspectives, and experiences, and fostering inclusion that inspires innovation, encourages respect and promotes unlimited success. Our goal is to attract and sustain a diverse workforce by recruiting, hiring, developing and retaining high-performing employees who work collaboratively to carry out the mission of MMI.

Individuals seeking employment with MMI that have any Criminal Offender Record Information remain eligible for employment subject to applicable law and regulation

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We are a patient first focused organization providing top quality medical cannabis in a compassionate, warm environment. We aim to be an employer of choice and as such offer a robust compensation package including competitive salary, full medical benefits, and employee discounts!</p><p><b>Summary</b></p><p>The Quality Engineer I is a technical professional position, reporting to the Quality Manager. The Quality Engineer will be focused on defining, measuring, improving and maintaining product quality through improvements in our production processes, equipment and employee skills. In this regard, they will be the subject matter expert and authority at their site or region on all matters that are quality related.</p><p>A qualified candidate will be analytical, have extensive cross-functional experience, is a seasoned operator, influencer, and collaborator, and will have a track record of operating within a mature manufacturing system.</p><p>Essential Responsibilities</p><p>• Work with the Manager to define quality metrics: specific, measurable and relevant.</p><p>• Establish quality control points -- throughout the cultivation and processing system -- for the above metrics</p><p>• Lead a cross functional team to identify quality improving projects and then drive the top projects to deliver results</p><p>• Evaluate proposed process or equipment changes for potential impact on quality</p><p>• Be the site’s or region’s subject matter expert on quality control and assurance</p><p>• Work with Manager to develop and/or enhance manufacturing processes and controls and the capturing of quality control data.</p><p>• Work with the Manager to select and implement a software-based platform for capturing and dashboarding quality control metrics. This may include but is not limited to developing within the ERP, the data capturing methods and tools necessary to report status upwards. As needed, this will include the deployment of data capturing sensors and test equipment.</p><p>• Drive the investigation of out-of-control processes, identify root cause and implement improvements to significantly reduce the frequency and/or impact of future occurrences</p><p>• As needed, provide due diligence support with respect to any acquisition of a new operation. This would include but not be limited to the evaluation of the scope and span of quality systems.</p><p>• Keep informed of the best quality practices within and without iAnthus and drive the adoption of them</p><p>• Establish a cadence for communicating in a timely and concise way the status of metrics, projects, issues, etc.</p><p>• Ensure a safe work environment and a culture that embraces safe work habits, understanding of the risks, compliance with regulations, and prioritizing corrective action of any identified safety hazards or risks</p><p>• Ensure Team Members have the tools, knowledge, and equipment required to do their jobs</p><p>• Ensure that the Quality systems, testing and compliance of all company products facilitates brand leadership and exceeds legal requirements and leads to delighted customers.</p><p>Education and Skills Requirements</p><p>• Must be at least 21 years old</p><p>• A bachelor’s degree in Engineering or Science with appropriate training in manufacturing and quality control methods preferred.</p><p>• An exception to the B.S. degree will be considered when a candidate presents a great attitude and aptitude to learn analytical skills that are common to quality professionals (e.g., basic statistics, SPC, spreadsheet usage, experiment design, etc.)</p><p>• Green belt certification in Lean Manufacturing or a basic introductory course and equivalent experience</p><p>• Minimum of 2 years of industrial experience where quality was part of the culture</p><p>• Minimum of 2 years’ experience as a team leader or Supervisor</p><p>• Project management experience which includes being proficient with project management tools such as Microsoft Project.</p><p>• An effective and persuasive communicator that constantly strives for simplicity and clarity.</p><p>Physical and Environmental Requirements</p><p>• Ability to work a minimum of 10 hours a day and rotating shifts;</p><p>• Flexible schedule availability including nights, weekends and holidays;</p><p>• Ability to lift, push, and pull 50 pounds;</p><p>• Ability to sit, squat, bend, and kneel repetitively throughout a work day;</p><p>• Ability to stand for extended periods of time;</p><p>• Ability to use a ladder (up to 12 ft. extension) and general hardware tools needed for common repairs;</p><p><b>• Ability and willingness to work in the following conditions:</b></p><p>• General office environment;</p><p>• Extended computer usage;</p><p>• Extended phone usage including teleconferences, and</p><p>• Work environments that include exposure to, but not limited to, fumes, dust, odors, heights, indoor AC, no AC, motion, and noise.</p><p>MMI encourages applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. MMI believes in creating and sustaining a robust policy of inclusivity and diversity. MMI recognizes that diversity in the workforce is key to the integrity of a company’s commitment to its community. MMI’s Diversity &amp; Inclusion Plan is designed to promote equity among minorities, women, veterans, people with disabilities, and people who identify as LGBTQ+. MMI will make every effort to employ and advance in employment qualified and diverse people at all levels within the company.</p><p>We value all team members by embracing their diverse talents, perspectives, and experiences, and fostering inclusion that inspires innovation, encourages respect and promotes unlimited success. Our goal is to attract and sustain a diverse workforce by recruiting, hiring, developing and retaining high-performing employees who work collaboratively to carry out the mission of MMI.</p><p>Individuals seeking employment with MMI that have any Criminal Offender Record Information remain eligible for employment subject to applicable law and regulation</p></div>","company":{"companyType":"Public/Established","name":"iAnthus Capital","logoUrl":"/logos/ianthus-capital-c36caf6d20991ec90c6c56824883f16e.png"},"location":{"country":"United States","address":"Holliston, MA, USA","city":"Holliston","stateProvince":"MA"},"frontendLink":"/job-posting/ianthus-capital/quality-engineer/c861c9e0fcecf524ba50fabd846efbd6","title":"Quality Engineer","category":"Medical & Healthcare","hash":"c861c9e0fcecf524ba50fabd846efbd6","postingUrl":"https://ianthuscapital.applytojob.com/apply/JBwAs5FobW/Quality-Engineer","salary":"$67k - $110k"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"2 days ago","description":"<div><div><p>Description</p><div>Driven by a love of plants, Pure Sunfarms is one of Canada’s largest, single-site, licensed producers of high-quality, greenhouse-grown cannabis based in BC’s Fraser Valley (Delta). We are proud to bring together individuals from a wide breadth of industries, backgrounds, and experiences, and promote a culture of belonging where everyone can truly be themselves – in every form of expression that is natural to them. This is our priority and guiding light at Pure Sunfarms, driving our uncompromising approach to quality and success within the Canadian recreational cannabis market. We believe our differences are our strengths, letting us look at cannabis in a whole new light.</div><div></div><div><br />Pure Sunfarms is looking for a Quality Assurance Technician to join a team of Quality, Regulatory and Research professionals. This is a dynamic role for anyone looking to gain a combination of knowledge/experience in cannabis cultivation/processing, quality management system and Cannabis Regulations. The QA Tech will primarily be responsible for the complaint management process and assist manager/director of QA to analyze the safety/quality/compliance of concerned products. The QA Tech will partner cross-functionally with internal stakeholders, including but not limited to Customer Care, Quality, Operations and Manufacturing, and external stakeholders including wholesale customer and co-manufacturing Licence holders.</div><div><p>Essential Functions</p><ul><li>Communicate any complaint information to relevant internal/external stakeholders</li><li>Partner closely with Quality/Production colleagues to investigate product quality concerns, perform root cause analysis</li><li>Initiate corrective action plans and coordinate with Quality/Production colleagues to address each action item. Follow up on any action items until completion</li><li>Highlight and identify trends to be further reviewed, investigated, or actioned by management</li><li>Ensure that complaints are investigated, resolved, and closed in a timely manner</li><li>Maintain Compliant documents, including but not limited to logging complaints into ERP system/provincial board portal, complete complaint reports, and update complaint status.</li><li>Assist with SOPs, CAPA (corrective action &amp; preventive action), change control, deviation related to complaint processes.</li></ul><p>Other Duties</p><ul><li>We work in a fast-paced environment, rolling up our sleeves to build something bigger than ourselves. Other duties may arise from time to time/most of the time and as a team, we look to support each other.</li></ul><p>Your Brand, Your Story</p><ul><li>We already know you love working with data and sample collection, but we want to know more about your strengths. You’re good at the following:</li><li>Bachelor’s Degree in Science or related field of study, AND/OR equivalent combination of education and experience</li><li>Knowledge of applicable federal and provincial legislation, acts and regulations for Cannabis would be an asset</li><li>Experience in developing SOPs, work instructions, and drafting technical reports</li><li>Experience in handling customer complaints, change control, CAPA.</li><li>QA work experience in a GMP environment would be an asset</li><li>Strong analytical, and problem-solving skills with a focus on details, while working in a dynamic, fast-paced environment</li><li>Proficient in the use of Microsoft Office (Word, Excel, PowerPoint, Outlook)</li><li>Demonstrated good verbal and written communication skills in English</li><li>Organizing and prioritizing your work to meet deadlines and can adapt to unexpected priorities</li><li>Exercising professional judgement and decision making</li><li>Must have the ability to obtain and pass a RCMP Criminal Record Check and maintain security clearance.</li></ul></div><p>Additional</p><div>At Pure Sunfarms, we are growing our team with the same care we devote to growing our plants. We’re proud of the diverse and inclusive culture that we’ve built and are excited to learn more about your experiences and how you can contribute to Pure Sunfarms and the cannabis industry.</div></div></div>","company":{"companyType":"Private/Established","name":"Pure Sunfarms Corporation","logoUrl":"/logos/pure-sunfarms-corporation-c66da2f25a44a5e7747d36cca5a40fc8.jpeg"},"location":{"country":"Canada","address":"Delta, BC","city":"Delta","stateProvince":"BC"},"frontendLink":"/job-posting/pure-sunfarms-corporation/quality-assurance-technician/30b1ebf580c83b4ae6a52923bf60cd7d","title":"Quality Assurance Technician","category":"Agriculture & Farming","hash":"30b1ebf580c83b4ae6a52923bf60cd7d","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-e93e8bd0c9771905"},{"employmentType":"Full-time, Permanent","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"2 days ago","description":"<div><p><b>Quality Assurance Associate</b></p><p><b>Reports To: </b>Quality Assurance Manager</p><p><b>Position Summary</b></p><p>The Quality Assurance Associate is responsible for providing support to the Quality Assurance team. S/he will assist with document management, data entry, and administrative support related to Quality Assurance. S/he will aid in the ongoing implementation and monitoring of the quality assurance systems.</p><p><b>Core Competencies</b></p><ul><li>Detail Oriented</li><li>Ethical</li><li>Regulatory Compliant</li><li>Team Player</li><li>Accountability</li><li>Analytical Thinking</li></ul><ul><li>Collaborative</li><li>Problem Solving</li><li>Communication</li><li>Understand SOP’s</li><li>Customer oriented</li><li>Work independently</li></ul><p><b>Job Duties</b></p><ul><li>Serve as an integral member of the Quality Assurance team, interact cross-functionally to ensure business objectives are aligned, and ensure that the organization meets its quality and business objectives</li><li>Assist in Quality Assurance activities and ensure compliance with Health Canada’s guidelines pertaining to production, processing, packaging, labeling, and shipping</li><li>Prepare and modify documents including correspondence, reports, drafts, memos, and emails</li><li>Scan, print, and photocopy QA documents</li><li>Create QA-related materials such as signs and logbooks</li><li>Complete basic data entry</li><li>Maintain accurate record keeping</li><li>Responsible for organizing and filing controlled documents</li><li>Prepare SOPs to be completed by staff during onboarding and after revisions</li><li>Assist with in-house and regulatory audits</li><li>Assist in the preparation of QA deliveries and facilitate shipments</li><li>Read and follow written and verbal work instructions</li></ul><p>· Ensure compliance with safe work practices, Standard Operating Procedures, and all applicable regulations</p><ul><li>Assist in any task the Head of Facilities designates as an immediate priority to preserve the physical or environmental security of the building, contents, or staff</li><li>Attend any training session designated by the Company</li><li>Other duties may be assigned from time to time</li></ul><p><b>Qualifications</b></p><ul><li>Bachelor of Science Degree (BSc) in applicable field.</li><li>2-5 years of work experience in a related field required.</li><li>Knowledge of GPP, GMP, ISO 9001, and Health Canada cannabis regulations.</li><li>Previous experience in either the cannabis or pharmaceutical industry an asset.</li><li>Laboratory experience an asset.</li><li>Knowledge and experience in chemistry, and pharmacology an asset.</li><li>Strong knowledge of MS Word, Excel, and Outlook.</li><li>Excellent analytical skills and above-average attention to detail.</li><li>Excellent time management and prioritization skills.</li><li>Capable of multitasking with minimal supervision.</li><li>Excellent English communication skills, both written and verbal.</li><li>Ability to complete a satisfactory criminal record check.</li><li>Reliable attendance is mandatory</li><li>Excellent workplace housekeeping is essential</li><li>Team worker able to co-exist with other staff and assist whenever able</li><li>Strong attention to detail</li><li>Able to work independently once given a task</li></ul><p><b>Working Conditions</b></p><ul><li>Available for work on the weekends as needed</li><li>PPE Required: Scrubs, gloves, hairnets, and safety shoes</li></ul><p>Application deadline: 2021-09-22</p><p>Expected start date: 2021-09-24</p><p>Job Types: Full-time, Permanent</p><p>Salary: $1.00 per year</p><p>Additional pay:</p><ul><li>Overtime pay</li></ul><p>Benefits:</p><ul><li>Dental care</li><li>Extended health care</li><li>On-site parking</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>Experience:</p><ul><li>Quality assurance: 2 years (preferred)</li><li>Cannabis Industry or Regulatory: 1 year (preferred)</li></ul></div>","company":{"name":"Heritage Cannabis Holdings- Voyage"},"location":{"country":"Canada","address":"Falkland, BC","city":"Falkland","stateProvince":"BC"},"frontendLink":"/job-posting/heritage-cannabis-holdings-voyage/quality-assurance-associate/271466ab6e69416c0c38ac0690445cb3","title":"Quality Assurance Associate","category":"Professional, Scientific, and Technical Services","hash":"271466ab6e69416c0c38ac0690445cb3","postingUrl":"https://ca.indeed.com/job/quality-assurance-associate-03bf4cd2e10164a7"},{"softSkills":["Analytical","Communication","Organization"],"benefits":null,"employmentType":"Full-time","values":["Accountability","Autonomy","Hard work"],"description":"<p><span style=\"color: rgba(0, 0, 0, 0.9);\">Velvet is a privately-owned company with a brokerage/agency model, representing Licensed Producers in the Cannabis industry in Canada. We represent our Licensed Producers at all levels of selling and marketing to government buyers and private retailers. We are looking for industry leaders to join us as we work to build the best cannabis agency in the industry.</span></p><p><br></p><p><span style=\"color: rgba(0, 0, 0, 0.9);\">As a Portfolio Brand Manager, you will report directly to the Vice President of Brand Portfolio and will act as the primary point of contact with the suppliers. We are looking for a person who loves challenges, is well educated when it comes to the cannabis industry and thrives in an entrepreneurial environment.</span></p><p><span style=\"color: rgba(0, 0, 0, 0.9);\"> </span></p><p><span style=\"color: rgba(0, 0, 0, 0.9);\">Responsibilities</span></p><p><br></p><ul><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Manage a portfolio of partner brands. Act as the key contact in Canada for these partners while building harmonious, value-based, business relationships with them.</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Develop and implement annual business plans in collaboration with the sales team to achieve expected sales and revenue targets.</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Define Key SKUs and priorities with the LPs</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Build annual forecast in collaboration with commercial sales director and LPs</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Develop sales and trade marketing activities to support sales</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Continuously review results versus annual plan, implementing corrective measures where necessary. Report back on progress monthly and quarterly to LPs.</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Compile and organize information from the suppliers for tenders.</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Overview the execution of sales & marketing tools as defined in the marketing plan</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Build presentation to guide the sales team</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Assist with the organization of different events (training, industry events, etc…)</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Analyse category data, gather competitive intelligence, and identify key consumer and marketing trends to make recommendations that will foster partner growth.</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Assist the Vice President and the Sales director with building presentations (product launch plan, retailers’ meetings, category review etc.)</span></li></ul><p><span style=\"color: rgba(0, 0, 0, 0.9);\"> </span></p><p><span style=\"color: rgba(0, 0, 0, 0.9);\">Education and experiences </span></p><p><span style=\"color: rgba(0, 0, 0, 0.9);\"> </span></p><ul><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Bachelor''s degree in business administration, marketing specialization or equivalent.</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Five (5) years of experience in marketing or trade marketing.</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Experience in cannabis or the alcoholic beverage industry an asset.</span></li></ul><p><span style=\"color: rgba(0, 0, 0, 0.9);\"> </span></p><p><span style=\"color: rgba(0, 0, 0, 0.9);\">Qualifications </span></p><p><br></p><ul><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Strong interpersonal skills</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Customer oriented</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Highly organized and attention to details</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Strong communication skills</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Ability to build strong presentations</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Ability to work under pressure</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Creative and innovative</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Autonomous and sense of initiative</span></li></ul><p><br></p><p><span style=\"color: rgba(0, 0, 0, 0.9);\">Technical skills</span></p><p><br></p><ul><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Bilingual (English and French), both written and oral.</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Excellent knowledge of Microsoft Office Suite, particularly Excel and Power Point</span></li><li><span style=\"color: rgba(0, 0, 0, 0.9);\">Knowledge and passion for cannabis is an asset</span></li></ul><p><br></p>","title":"Portfolio Brand Manager","salaries":null,"ccApplicationTypeInput":"[email protected]","function":["Data & Analytics","Professional Services","Project Management"],"postedOn":"5 days ago","company":{"website":"https://velvetmanagement.com/","companyType":"Startup","name":"Velvet Management Inc.","_id":"6015a011-1b96-4a6f-a16a-8879a9c03401","logoUrl":"/logos/velvet-management-inc-f5259d01208bc48be8dadb3ebc84649c.jpeg"},"location":{"country":"Canada","address":"Montreal, Quebec, Canada","city":"Montreal","stateProvince":"Quebec"},"frontendLink":"/job-posting/velvet-management-inc/portfolio-brand-manager/921489e51e8fa015f186336915076c87","category":["Retail"],"hardSkills":{"Sales":["Account Management","Microsoft Office"],"Business Development":["Business Intelligence"]},"hash":"921489e51e8fa015f186336915076c87","ccApplicationType":"email"},{"salaries":[{"salaryStart":"$79k","salaryEnd":"$170k","currency":"US","source":"LawCrossing.com","position":"General Counsel Chief Compliance Officer","type":"per year","url":"https://www.lawcrossing.com/salaries/q-general-counsel-chief-compliance-officer-l-Philadelphia-PA-jobs.html"},{"salaryStart":"$120k","salaryEnd":"$470k","currency":"US","source":"Glassdoor","position":"Legal Counsel And Chief Compliance Officer","type":"per year","url":"https://www.glassdoor.com/Salaries/new-york-city-legal-counsel-and-chief-compliance-officer-salary-SRCH_IL.0,13_IM615_KO14,56.htm"},{"salaryStart":"$47k","salaryEnd":"$190k","currency":"US","source":"ZipRecruiter","position":"Chief Privacy Officer","type":"per year","url":"https://www.ziprecruiter.com/Salaries/Chief-Privacy-Officer-Salary-in-Philadelphia,PA"}],"employmentType":"Contractor","function":["Legal"],"postedOn":"3 days ago","description":"<div><p>Maitri Medicinals is a medical cannabis company located in Pennsylvania. Our mission is to cultivate, produce and dispense quality medical marijuana products for Pennsylvania patients who suffer from qualifying medical conditions and diseases.A growing Pennsylvania based Cannabis company is seeking Corporate Counsel to join our team. The Corporate Counsel reports directly to the CEO and is responsible for leading strategic legal and risk initiatives of the company. The candidate selected must be meticulously detail-oriented, motivated, and driven. The candidate must be flexible enough to adjust with a changing industry while balancing legal risks and business concerns.Responsibilities:Provide legal support to internal stakeholders including Sales, Vendor Relations, Finance, and Executive-level management.Legal point of contact for the company's customer and vendor contract needs.Structuring, drafting and negotiating a wide range of complex technology agreements including master services agreements, professional services agreements, sales orders, and non-disclosure agreements, and coordinate involvement of all necessary cross-functional business and technology constituents.Advise on contract status, legal risks, and the legal liabilities associated with different deals.Review, revise and negotiate a variety of other commercial and vendor agreements.Work with and advise executives within the Company on a variety of legal and compliance issues in both commercial and public sectors.Extensive knowledge of Federal, State and Local Employment LawsQualifications:J.D. and excellent academic credentialsMember in good standing of PA state bar associationHeavy emphasis on Employment LawExperience with Contract Law2+ years of corporate and transactional legal experience with Cannabis Business or relatedSignificant contract review and negotiation experienceAbility to work both collaboratively and independently as required by task, building and maintaining strong relationshipsExcellent organizational skills, ability to manage multiple projects at once, follow through and meet deadlinesUrgency and results focus to ensure timely and appropriate response to issues raised; andStrong written and oral communication skillsStrong analytical and computer skillsMaitri is an Equal Opportunity Employer. Maitri does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.Powered by JazzHR</p></div>","company":{"companyType":"Private/Growth","name":"Maitri Medicinals"},"location":{"country":"United States","address":"Lansdale, PA, USA","city":"Lansdale","stateProvince":"PA"},"frontendLink":"/job-posting/maitri-medicinals/corporate-counsel-and-compliance-officer/f8353d90c9a311ea44f389d796c510ab","title":"Corporate Counsel and Compliance Officer","category":"Medical & Healthcare","hash":"f8353d90c9a311ea44f389d796c510ab","postingUrl":"https://www.linkedin.com/jobs/view/corporate-counsel-and-compliance-officer-at-maitri-medicinals-2769167165","salary":"$79k - $170k"},{"salaries":[{"salaryStart":"$82k","salaryEnd":"$130k","currency":"US","source":"Salary.com","position":"Quality Assurance Manager","type":"per year","url":"https://www.salary.com/research/salary/benchmark/quality-assurance-manager-salary/tallahassee-fl"},{"salaryStart":"$27k","salaryEnd":"$73k","currency":"US","source":"ZipRecruiter","position":"Quality Assurance Specialist","type":"per year","url":"https://www.ziprecruiter.com/Salaries/Quality-Assurance-Specialist-Salary-in-Tallahassee,FL"},{"salaryStart":"$50k","salaryEnd":"$130k","currency":"US","source":"Glassdoor","position":"QA Manager","type":"per year","url":"https://www.glassdoor.com/Salaries/dothan-qa-manager-salary-SRCH_IL.0,6_IM241_KO7,17.htm"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"4 days ago","description":"<div><p>Quality Assurance LeadDescriptionJob Title: Quality Assurance LeadDepartment: Quality Assurance - CultivationReports to: Quality Assurance Supervisor- CultivationFLSA Status: Regular - Non-ExemptLocation: Quincy, FLRole Summary: The Quality Assurance Shift Lead-Cultivation will be responsible for facilitating workflow between Flower Tech's and QA Tech's. Along with ensuring each QA Tech has enough product to scan at any given time, the QA Lead will monitor quality of scans to ensure material is being properly and effectively separated as needed. The QA Lead work in conjunction with the Flower Tech Supervisor to ensure proper tracking of cleared and adulterated weight. Other duties and responsibilities will include, but not be limited to:Key Duties and ResponsibilitiesApproves incoming materials by confirming specifications; conducting visual scans on product scanned by QA TechsApproves finished products by confirming specifications; conducting visual scans and returning products for re-work; confirming re-work.Documents inspection results by completing reports and logs; summarizing re-work and waste; inputting data into quality database.Maintains a safe and healthy work environment by following cGMP Standard Operating Procedures; complying with legal regulations.Ensure product is scanned/handled in accordance with the proper Standard Operating Procedure's (SOP)Direct activities and resources of the quality department to meet company objective of producing highest quality product.Continuous Improvement to maximize product quality and minimize costs.Provide feedback as neededTrain employees as requiredTake active role in investigating and resolving problems related to quality.Performs other duties as required.Position RequirementsSKILLS AND QUALIFICATIONS:At minimum, a high school diploma.1-3 years' experience in the quality field or similar experience.Technical proficiency must be able to use computers and generate reports.Ability to analyze data and create and review processes.Excellent communication skills.A desire to help others achieve their best.Experience in a team lead position preferred.Must be able to lead projects/people, motivate associates and proactively anticipate and address issues.ADDITIONAL MINIMUM QUALIFICATIONS:High school diploma or equivalent requiredMust be a minimum of 21 years of ageMust have valid Florida Driver's Licenser or ability to obtain oneMust successfully complete a comprehensive background screeningPHYSICAL REQUIREMENTS:Must be able to push, pull, move, and/or lift a minimum of 50 lbs. 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. 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. (Moderate noise)WORK SCHEDULE:40+ hours weekly with flexible hours depending on department needs. Must be available to work occasional evenings, weekends, and holidaysEqual Opportunity Employer l Trulieve Supports a Drug Free WorkplaceFull-Time/Part-TimeFull-Time ShiftVarious Shifts Level 2 Background check requiredPositionQuality Assurance Lead DivisionTrulieve, INC Close DatePost Internal Days0 Number of Openings1 Number Filled0 Exempt/Non-ExemptNon-Exempt Req NumberCUL-21-00204 Open Date6/14/2021 LocationHigdon EOE StatementWe are an equal employment opportunity employer. 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. This position is currently accepting applications.</p><p>Associated topics: performance test, qa, quality assurance analyst, quality assurance engineer, quality assurance lead, software quality, software quality assurance, software quality assurance engineer, test, tester</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-lead/6b5a45937c47a1d65d0e02ddafc44998","title":"Quality Assurance Lead","category":"Medical & Healthcare","hash":"6b5a45937c47a1d65d0e02ddafc44998","postingUrl":"https://www.rapidinterviews.com/job/quality-assurance-lead-with-trulieve-cannabis-in-quincy-j2c-1779","salary":"$82k - $130k"},{"employmentType":"Full-time","function":["Legal"],"postedOn":"2 days ago","description":"<div><p>BeLeaf Medical is a vertically integrated Missouri medical cannabis company. BeLeaf is dedicated to providing Missouri patients consistent and high-quality medical marijuana in the forms of smokable flower, concentrates, and consumable products. BeLeaf owns Sinse, Phytos, and Swade brands, and partners with dispensaries throughout the state to broaden geographical reach. The Compliance Officer will be a key part of the Beleaf team.</p><p>Description</p><p>The Safety &amp; Compliance Officer advises and consults with managers and contractors to identify and resolve problems or conflicts, define areas for enhancements, cross-functional efficiencies, and improvement, and identify approaches and plans to meet/exceeds objectives. Make sure that Beleaf Medical conforms to contractual obligations, government regulations, and laws.</p><p>Duties/Responsibilities:</p><ul><li>Review and develop SOPs with department managers.</li><li>Maintain regulatory knowledge applicable to the position to include being the point of contact for DHSS.</li><li>Review contracts and prepare legal documents and notices.</li><li>Training facilitator for compliance and safety.</li><li>Initiate and organize OSHA training for employees.</li><li>Conduct risk assessment and enforce preventative measures.</li><li>Investigate any OSHA or worker’s comp reports, in cooperation with HR.</li><li>Implement and maintain site specific safety procedures.</li><li>Implement and maintain a safety drill protocol for all locations.</li><li>Lead the organizations performance improvement efforts as they relate to safety and compliance.</li><li>Maintain an up-to-date safety manual, including all necessary site-specific procedures.</li><li>Performs other related duties as assigned.</li></ul><p>Required Skills/Abilities:</p><ul><li>Excellent verbal and written communication skills.</li><li>Excellent organizational skills and attention to detail.</li></ul><ul><li>Excellent time management skills with a proven ability to meet deadlines.</li><li>Ability to function well in a high-paced and at times stressful environment.</li><li>Good knowledge of legal requirements and procedures.</li></ul><p>Education and Experience:</p><ul><li>Master’s degree in law, legal studies, or related field. J.D. degree preferred.</li><li>3-5 years’ experience in a compliance role</li></ul><p>Physical Requirements:</p><ul><li>Prolonged periods of sitting at a desk and working on a computer.</li><li>Must be able to lift up to 15 pounds at times.</li></ul><p>Please apply at: https://www.beleafmedical.com/careers</p><p>Job Type: Full-time</p><p>Pay: $95,000.00 - $100,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>Dental insurance</li><li>Flexible schedule</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>Monday to Friday</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul><p>Work Location: One location</p></div>","company":{"companyType":"Private/Established","name":"Beleaf Medical","logoUrl":"/logos/beleaf-medical-c4ea1279406fd18ae9dbfc4a20bf33c8.png"},"location":{"country":"United States","address":"Saint Charles, MO 63303","city":"Saint Charles","stateProvince":"MO"},"frontendLink":"/job-posting/beleaf-medical/compliance-officer/a57658b847129d31f2cab3c8e604c2a5","title":"Compliance Officer","category":"Agriculture & Farming","hash":"a57658b847129d31f2cab3c8e604c2a5","postingUrl":"https://www.indeed.com/job/compliance-officer-bb3feca53a3ba3fa"},{"function":["Legal"],"postedOn":"4 days ago","description":"<div><p></p><div><p>Maitri Medicinals is a medical cannabis company located in Pennsylvania. Our mission is to cultivate, produce and dispense quality medical marijuana products for Pennsylvania patients who suffer from qualifying medical conditions and diseases.</p><p>A growing Pennsylvania based Cannabis company is seeking Corporate Counsel to join our team. The Corporate Counsel reports directly to the CEO and is responsible for leading strategic legal and risk initiatives of the company. The candidate selected must be meticulously detail-oriented, motivated, and driven. The candidate must be flexible enough to adjust with a changing industry while balancing legal risks and business concerns.</p><p>Responsibilities:</p><ul><li>Provide legal support to internal stakeholders including Sales, Vendor Relations, Finance, and Executive-level management.</li><li>Legal point of contact for the company's customer and vendor contract needs.</li><li>Structuring, drafting and negotiating a wide range of complex technology agreements including master services agreements, professional services agreements, sales orders, and non-disclosure agreements, and coordinate involvement of all necessary cross-functional business and technology constituents.</li><li>Advise on contract status, legal risks, and the legal liabilities associated with different deals.</li><li>Review, revise and negotiate a variety of other commercial and vendor agreements.</li><li>Work with and advise executives within the Company on a variety of legal and compliance issues in both commercial and public sectors.</li><li>Extensive knowledge of Federal, State and Local Employment Laws</li></ul><p>Qualifications:</p><ul><li>J.D. and excellent academic credentials</li><li>Member in good standing of PA state bar association</li><li>Heavy emphasis on Employment Law</li><li>Experience with Contract Law</li><li>2+ years of corporate and transactional legal experience with Cannabis Business or related</li><li>Significant contract review and negotiation experience</li><li>Ability to work both collaboratively and independently as required by task, building and maintaining strong relationships</li><li>Excellent organizational skills, ability to manage multiple projects at once, follow through and meet deadlines</li><li>Urgency and results focus to ensure timely and appropriate response to issues raised; and</li><li>Strong written and oral communication skills</li><li>Strong analytical and computer skills</li></ul><p>Maitri is an Equal Opportunity Employer. Maitri does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.</p><p></p><p>qgvevmZM1v</p></div></div>","company":{"companyType":"Private/Growth","name":"Maitri Medicinals"},"location":{"country":"United States","address":"Pittsburgh, PA 15238","city":"Pittsburgh","stateProvince":"PA"},"frontendLink":"/job-posting/maitri-medicinals/corporate-counsel-and-compliance-officer/004775519b4a7f4fb5705ca7080cc927","title":"Corporate Counsel and Compliance Officer","category":"Medical & Healthcare","hash":"004775519b4a7f4fb5705ca7080cc927","postingUrl":"https://www.indeed.com/job/corporate-counsel-and-compliance-officer-f204dedff5c8a8ce"},{"employmentType":"Full-time, Permanent","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"3 days ago","description":"<div><p><b>QA Documentation Clerk</b></p><p>ZYUS is a Canadian-based, next-generation life sciences company leading scientific research and development in phyto-therapeutics. We are committed to delivering high-quality standardized therapeutic formulations that comply with Good Manufacturing Practices (GMP) to provide targeted relief for our patients.</p><p>We aim to shift the paradigm from conventional strategies to focus on improving our patients’ overall quality of life and well-being by harnessing the power of cannabinoids. With science as our driver, we can reimagine the potential of phyto-therapeutics by investing in medical research, clinical trials, and advanced process manufacturing. Together, we can establish phyto-therapeutics as a standard of care to restore health and manage disease.</p><p>At ZYUS, we are forging a new industry of phyto-therapeutics by elevating cannabinoid formulations as a standard of care and reimagining the potential of protein-based formulations – in pursuit of transformational impact on patient lives.</p><p><b>ZYUS. Advancing the science of well-being.</b></p><p>Join us on our mission.</p><p><b>Your Contribution </b></p><p>· Control document revisions and storage of documents, including SOP’s, Protocols, Product Batch Records, Deviations and Complaints.</p><p>· Track and update the SOP system to ensure adequate tools are available for appropriate training and understanding.</p><p>· Track training records of colleagues.</p><p>· Print, scan, and file documents/records.</p><p>· Review procedures, work instructions, protocols, and forms for format consistency.</p><p>· Perform records review.</p><p>· Retrieve documents as requested during inspectorate visits.</p><p>· All other duties as assigned.</p><p><b>What it Takes</b></p><p>· Secondary education, preferably a Diploma in a related field.</p><p>· Minimum of 1 year experience, preferably in a regulated manufacturing environment.</p><p>· Proficiency with Microsoft Office applications (Word, Excel, Outlook, etc.).</p><p>· Excellent organizational and analytical skills.</p><p>· Motivated individual with a high level of integrity.</p><p>· Excellent written and oral communication skills is required.</p><p>· Knowledge of quality assurance and the Cannabis Regulations, Food &amp; Drug Regulations, and Narcotic Control Regulations is an asset.</p><p>· Knowledge of Good Documentation Practice and Good manufacturing Practice (GMP) is an asset.</p><p><b>Benefits of Joining Our Team</b></p><p>At ZYUS, we care about our people. Our total rewards package includes comprehensive benefits, retirements savings, paid time off, on-going training and development opportunities.</p><p>Application deadline: 2021-11-05</p><p>Job Types: Full-time, Permanent</p><p>Additional pay:</p><ul><li>Bonus pay</li><li>Overtime pay</li></ul><p>Benefits:</p><ul><li>Company events</li><li>Dental care</li><li>Disability insurance</li><li>Employee assistance program</li><li>Employee stock purchase plan</li><li>Extended health care</li><li>Life insurance</li><li>On-site gym</li><li>On-site parking</li><li>Paid time off</li><li>Stock options</li><li>Store discount</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"name":"ZYUS Life Sciences Inc."},"location":{"country":"Canada","address":"Saskatoon, SK","city":"Saskatoon","stateProvince":"SK"},"frontendLink":"/job-posting/zyus-life-sciences-inc/quality-assurance-documentation-clerk/b9f40fbd78d5be8316d93030481756dd","title":"Quality Assurance Documentation Clerk","category":"Manufacturing","hash":"b9f40fbd78d5be8316d93030481756dd","postingUrl":"https://ca.indeed.com/job/quality-assurance-documentation-clerk-ab77de151671bde1"},{"employmentType":"Full-time, Permanent","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"4 days ago","description":"<div><p>The Quality Control Associate will report to the Quality Assurance Specialist and will be responsible for providing quality oversight for site manufacturing operations. The QC Associate will be accountable for in-process quality monitoring of cannabis production processes in strict compliance with the Cannabis Regulations and Good Production Practices.  </p><p>ABOUT US:</p><p>BZAM is as awesome as it sounds! We are an integrated cannabis company that stands for quality, innovation, and integrity. Our commitment to excellence, service and employee satisfaction is demonstrated in our agile and strategic approach to market entry and our investment in people. As an emerging company with accomplished teams in leadership, growing and manufacturing, our focus on revolutionizing the space is the cornerstone of our business and portfolio development.</p><p>YOUR RESPONSIBILITIES:</p><ul><li>Ensure that all production activities are carried out as per Standard Operating Procedures (SOP) and in compliance with GPP; </li></ul><ul><li>Perform documentation review (i.e. batch manufacturing and/or packaging records, etc.) with high attention to detail using working knowledge of quality concepts and internal procedures;  </li></ul><ul><li>Enforce procedural and GPP requirements including health and hygiene, gowning, sanitation and documentation practices; </li></ul><ul><li>Coordinate change control implementation perform risk and impact assessment; </li></ul><ul><li>Review status of process materials and ensure proper control, hold, release and transfer of materials; </li></ul><ul><li>Assist in receiving inspections, verifications of BOMS and balances; </li></ul><ul><li>Perform environmental verifications, pre-line clearance, and in-process checks;  </li></ul><ul><li>Ensure that cannabis is destroyed as per current approved SOPs and in line with the Cannabis Regulations; </li></ul><ul><li>Ensure appropriate sample collection and testing; </li></ul><ul><li>Coordinate calibration, maintenance and pest control activities; </li></ul><ul><li>Provide assistance in resolving technical problems, process deviations, quality investigations, and corrective actions;  </li></ul><ul><li>Verify logs, databases, trends, and other data to track and flag quality concerns and areas of improvement; and </li></ul><ul><li>Other duties as assigned by Quality Assurance Manager &amp; Quality Assurance Specialist as applicable.  </li></ul><p>WHAT YOU BRING:</p><ul><li>BSc. in Chemistry, Biology, Pharmacology, Food Science, Microbiology or Environmental Science;  </li></ul><ul><li>Strong ethics coupled with respect for the highest compliance standards; </li></ul><ul><li>Strong and current knowledge of Good Agricultural Practice, Good Manufacturing Practice, regulatory and environmental guidelines as per the Cannabis Regulations;  </li></ul><ul><li>Problem-solving and decision-making skills; </li></ul><ul><li>Computer proficiency including MS Office; and </li></ul><ul><li>Excellent communication skills. </li></ul><p> </p><p>You Are FOCUSED, DETAIL ORIENTED, ORGANIZED 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>YOUR EXPERIENCE:</p><ul><li>2-3 years’ experience within a Quality Control position;  </li></ul><ul><li>Proven knowledge and experience in the stated responsibilities of the position (i.e. Food, Pharma, NHP); </li></ul><ul><li>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; and </li></ul><ul><li>Preferred experience with cGMP, GAP, GLP, HACCP, ISO and FDA. </li></ul><p>WHAT WE OFFER:</p><ul><li>Competitive Compensation</li></ul><ul><li>Extended Health and Dental Group Benefits and Health Care Spending Account*</li></ul><ul><li>RRSP Matching Program and TFSA options*</li></ul><ul><li>Rapid growth and advancement potential</li></ul><ul><li>Learning and development opportunities</li></ul><ul><li>Dynamic and innovative environment</li></ul><ul><li>Exceptional culture</li></ul><p>*Eligible employees</p><p>BZAM Cannabis 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.</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>Schedule:</p><ul><li>10 hour shift</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 Control: 2 years (preferred)</li><li>cGMP, GAP, GLP, HACCP, ISO and FDA: 1 year (preferred)</li></ul><p>Work remotely:</p><ul><li>No</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-control-associate/8878a9465fd0ee02317b32ad37b44311","title":"Quality Control Associate","category":"Agriculture & Farming","hash":"8878a9465fd0ee02317b32ad37b44311","postingUrl":"https://ca.indeed.com/job/quality-control-associate-04628f5a9614aba4"},{"salaries":[{"salaryStart":"$52k","salaryEnd":"$93k","currency":"US","source":"Glassdoor","position":"Data Analyst","type":"per year","url":"https://www.glassdoor.com/Salaries/portland-data-analyst-salary-SRCH_IL.0,8_IM699_KO9,21.htm"},{"salaryStart":"$34k","salaryEnd":"$95k","currency":"US","source":"ZipRecruiter","position":"Data Analyst","type":"per year","url":"https://www.ziprecruiter.com/Salaries/Data-Analyst-Salary--in-Maine"},{"salaryStart":"$47k","salaryEnd":"$74k","currency":"US","source":"Salary.com","position":"Entry Business Data Analyst","type":"per year","url":"https://www.salary.com/research/salary/alternate/entry-business-data-analyst-salary/me"}],"employmentType":"Full-time","function":["Data & Analytics"],"postedOn":"3 days ago","description":"<div><p>Job Title: Data Analyst</p><p>Company Background</p><p>Since 2013 MCR Labs has been your partner in cannabis science. Our team is made up of researchers, chemists, and pharmaceutical scientists, but we’re also enthusiasts, cannasseurs, and members of the cannabis community. We support the community by providing anyone interested in or passionate about cannabis with access to analytical product testing as well as information to help guide their cultivation, consumption, or enjoyment of marijuana, hemp, and cannabis-derived products.</p><p>As the first independent cannabis testing laboratory to be certified by the state of Massachusetts, we are proud to offer analytical testing and R&amp;D services to MMJ and adult-use cannabis providers, patients, doctors, caregivers, or anyone crafting their own cannabis products. Our methods are ISO-17025 accredited, and we employ proven analytical practices developed in the pharmaceutical industry.</p><p>MCR Labs is always looking for quality candidates to join our team of scientists and administrative personnel. The cannabis industry is one of the fastest growing jobs sectors in the nation, which allows us to consistently hire talented individuals who will develop and grow within our industry!</p><p><b>Summary</b></p><p>Data analyst works to ensure all data being generated by the laboratory is accurate and of the highest quality. This position is remote but will work with our newest lab in Gardiner, Maine.</p><p>Duties And Responsibilities</p><p>• Analyzing data generated by the laboratory personnel and analytical instruments.</p><p>• Quality control checking of all data generated by the laboratory.</p><p>• Being able to spot outliers and investigate anomalous instances of data.</p><p>• Issues statements of conformity or opinions or interpretations when necessary</p><p>• Work with the laboratory and quality assurance to ensure client complaints or issues are resolved in a timely and professional manner.</p><p>• Interpret analytical data including chromatograms.</p><p>• Input data to database such as LIMS and METRC.</p><p>• Generating and sending reports to various clients.</p><p>• Review and validate data processed by other data analysts</p><p><b>Qualifications</b></p><p>• Exceptional analytical, organization, problem solving and time management skills.</p><p>• Must be trained on all policies related to data analysis and reporting.</p><p>• Detail-oriented</p><p>• Strong ability to multi-task</p><p>• Ability to handle and analyze large datasets</p><p>• Proficient in MS Office</p><p>• Good communication skills</p><p>• Ability to identify procedural inadequacies or errors and communicate with the department to resolve the issue Requirements</p><p>• Ability to work flexible hours</p><p>• Minimum of BA/BS, with an emphasis on STEM fields with 1 year of experience or 5 years of experience in analytical data processing.</p><p>• Fully understand the navigation of LIMS to assist other departments, including but not limited to Client Service, Scientific Operations, and Laboratory Operations</p><p>• Great familiarity with client specific trends to raise questions on outliers in their samples</p><p>• Must be at least 21 years of age</p><p>• Must be able to pass background check.</p><p>• Advance data analytical skills with Excel</p><p>• Able to work in with a team and independently</p><p>MCR Labs is an equal opportunity employer. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, age, disability, sexual orientation, gender identity, sex, national origin, protected veteran status, or any other basis protected by federal, state, or local law.</p><p>Powered by JazzHR</p></div>","company":{"companyType":"Private/Growth","name":"MCR Labs","logoUrl":"/logos/mcr-labs-aed09bd7c5f16aa5e7ebc524f087c747.jpeg"},"location":{"country":"United States","address":"Gardiner, ME, USA","city":"Gardiner","stateProvince":"ME"},"frontendLink":"/job-posting/mcr-labs/data-analyst/a6fb35be929eea1ad2cc003f05b3b3c2","title":"Data Analyst","category":"Medical & Healthcare","hash":"a6fb35be929eea1ad2cc003f05b3b3c2","postingUrl":"https://www.linkedin.com/jobs/view/data-analyst-at-mcr-labs-2769365875","salary":"$52k - $93k"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"4 days ago","description":"<div><div><p><b>Location:</b> Franklin, MA</p><p></p><p><b><br />PARALLEL</b></p><p></p><p><b><br />Everyone is welcome here</b>. 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.</p><p></p><p><br />So, bring yourself and your best ideas; when we feel safe and comfortable being ourselves, there’s no limit to what we can achieve.</p><p></p><p><b><br />IN A NUTSHELL…</b></p><p></p><p><br />This role is to help drive the teams towards the day’s goals and help them prioritize or switch gears when necessary. Inventory Specialists play a critical role in ensuring that all monitoring of inventory is compliant with all RMD regulations.</p><p></p><p><br />This role is with NETA, 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.<br /></p><p></p><br /><p><b>WHAT YOU WILL BE DOING</b></p><p></p><ul><li><br />Daily maintenance of menu decisions, product storage, intake, and continuous live tracking with internal systems.</li><li>Provide product expertise and knowledge to PSAs and explain the potential benefits of various type products and strains of medical marijuana, as well as methods of use.</li><li>Responsible for performing any quality control checks as directed by the Inventory Director, Supervisor, Coordinator, or Dispensary Manager.</li><li>Responsible for accepting, tracking and processing all returns that occur at the point of sale; and daily reconciliation process.</li><li>Accurately perform inventory management, including processing product deliveries and restocking sales stations.</li><li>Maintain organized and consistent stocking and packaging systems for both existing and new products.</li><li>Communicate information to dispensary operation teams regarding inventory locations and any changes throughout the day. EXPERIENCE AND SKILLS YOU’LL BRING</li></ul><p></p><p><b><br />Required</b></p><p></p><ul><li>Age 21 or over</li><li>High school Diploma or equivalent</li><li>Valid Government-Issued Photo ID</li></ul><p></p><p><b><br />Preferred</b></p><p></p><ul><li>Strong communication skills.</li><li>Prior experience with Seed to Sale Systems or Virtual Gateway software.</li><li>Demonstrated ability to address situations and problem solve.</li><li>Must have full time open availability, every weekend availability.</li><li>Strong attention to detail, organizational skills and time management abilities.</li><li>Proficiency in windows-based software and Internet navigation.<br /></li></ul><p></p><br /><p><b>PHYSICAL REQUIREMENTS</b></p><p></p><ul><li><br />Ability to lift up to 50 lbs on occasion.</li><li>Ability to be able to be in constant standing/moving position.</li><li>Constantly operates a computer and other office productivity machinery.</li><li>The person in this position frequently communicates with other employees/customers.<br /></li></ul><p></p><br /><p><b>YOU WILL BE SUCCESSFUL IF YOU…</b></p><p></p><ul><li><br />Are self-motivated; micro-managing isn’t fun for anyone</li><li>Roll your sleeves up and do the work; strategy is important, but so is getting stuff done</li><li>Can work fast and be flexible; our industry is always changing</li><li>Play nice with others; we collaborate with each other a lot</li><li>Think creatively; sometimes, the “traditional” solution isn’t the best one</li></ul><p></p><p><b><br />WHAT YOU GET</b></p><p></p><ul><li><br />Consistent, reliable benefits; Full medical/vision/dental, 401k with possibility of a company match, access to company-sponsored well-being programs</li><li>Personal growth; industry-leading leadership and professional development offerings</li><li>Balance and flexibility; paid time off, paid parental leave, flexible work arrangements</li><li>Belonging and voice; employee resource groups, product advisory councils, monthly opportunities to share feedback and discuss your employee experience</li><li>Chance to make a difference; Employee Relief Fund, community volunteerism through our Parallel Cares program</li><li>Equity opportunity; ability to share in both the short-term and the long-term financial success of Parallel</li><li>Employee discount</li></ul><p></p><p><b><br />PARALLEL IS UNITED BY OUR VISION, MISSION, &amp; VALUES</b></p><p></p><p><b><br />Our Vision – </b>why we exist – is to pioneer well-being and improve the quality of life for humanity through the benefits of cannabinoids.</p><p><b>Our Mission –</b> 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.</p><p><b>Our Values –</b> Integrity | Collaboration | Alignment | Intentionality | Accountability | Agility</p><p></p><p><b><br />We are an Equal Opportunity Employer.</b> 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><p></p><p><b><br />DISCLAIMER</b></p><p></p><p><br />Parallel reserves the right to change or assign other duties to this job description. Your employment with Parallel is a voluntary one and is subject to termination by you or Parallel at will, with or without cause, and with or without notice, at any time. Nothing in this document shall be interpreted to be in conflict with or to eliminate or modify in any way the employment-at-will status of Parallel associates.</p><br />Internal ID: 43912_20211019</div></div>","company":{"companyType":"Public/Growth","name":"Neta"},"location":{"country":"United States","address":"Franklin, MA 02038","city":"Franklin","stateProvince":"MA"},"frontendLink":"/job-posting/neta/2247-quality-assurance-specialist/0f3a0365b9daa95c6720e0d0710b7be7","title":"2247 - Quality Assurance Specialist","category":"Professional, Scientific, and Technical Services","hash":"0f3a0365b9daa95c6720e0d0710b7be7","postingUrl":"https://www.indeed.com/job/2247-quality-assurance-specialist-439fec5f850d27ca"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"3 days ago","description":"<div><p>Our Client specializes in manufacturing cannabis pre-rolls in their facility in GTA West. The Quality Assurance Specialist (Health Canada Security Clearance) supports operations through the implementation and management of quality systems. They are responsible for ensuring the cannabis products produced meet the organization's objectives for quality, safety, regulatory, and customer expectations in accordance with the Cannabis Act &amp; relevant regulations. Note: This position requires an active Health Canada Security Clearance. Responsibilities: Work closely with the Production Manager to oversee the site QA and assist in developing, reviewing, and maintaining SOPs, Quality Management Programs, and projects to ensure compliance under the Cannabis Act/Regulations. Manage production records and labeling records. Work cross-departmentally to implement &amp; maintain SOPs (i.e. Operations, Regulatory, Security). Perform record-keeping tasks and document updates. Collect and review production Quality documents. Perform review, inspection, and/or validation of new materials and equipment. Support release of products through batch record compilation and review. Maintain current knowledge of best practices for the provisions of the Cannabis Act and Cannabis Regulations that apply to the license holder. Qualifications: Valid security clearance (ACMPR or Cannabis Regulations) is a strong requirement. BSc Degree in Chemistry, Biology, Pharmacology, or Food Science, obtained or recognized by a Canadian University. 4 years experience in Quality Assurance/Control in a production environment. Previous Cannabis Industry experience preferred. Preferred knowledge of plant chemistry, extraction and formulation systems, and chromatographic techniques. 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></div>","company":{"companyType":"Private/Startup","name":"Cannabis At Work","logoUrl":"/logos/cannabis-at-work-8ae63b190226a7031617f4393f916a20.jpeg"},"location":{"country":"Canada","address":"Toronto, ON","city":"Toronto","stateProvince":"ON"},"frontendLink":"/job-posting/cannabis-at-work/quality-assurance-specialist-health-canada-security-clearance/ae1b15e55787ab1f6a8d2c95ad4f24c6","title":"Quality Assurance Specialist (Health Canada Security Clearance)","category":"Professional, Scientific, and Technical Services","hash":"ae1b15e55787ab1f6a8d2c95ad4f24c6","postingUrl":"https://www.recruit.net/job/quality-assurance-specialist-jobs/2B467811A49CD203"},{"employmentType":"Full-time","function":["Data & Analytics"],"postedOn":"4 days ago","description":"<div><p>Job Title: Data Analyst</p><p><b>Company Background:</b></p><p>Since 2013 MCR Labs has been your partner in cannabis science. Our team is made up of researchers, chemists, and pharmaceutical scientists, but we’re also enthusiasts, cannasseurs, and members of the cannabis community. We support the community by providing anyone interested in or passionate about cannabis with access to analytical product testing as well as information to help guide their cultivation, consumption, or enjoyment of marijuana, hemp, and cannabis-derived products.</p><p>As the first independent cannabis testing laboratory to be certified by the state of Massachusetts, we are proud to offer analytical testing and R&amp;D services to MMJ and adult-use cannabis providers, patients, doctors, caregivers, or anyone crafting their own cannabis products. Our methods are ISO-17025 accredited, and we employ proven analytical practices developed in the pharmaceutical industry.</p><p>MCR Labs is always looking for quality candidates to join our team of scientists and administrative personnel. The cannabis industry is one of the fastest growing jobs sectors in the nation, which allows us to consistently hire talented individuals who will develop and grow within our industry!</p><p><b>Summary:</b></p><p>Data analyst works to ensure all data being generated by the laboratory is accurate and of the highest quality. This position is remote but will work with our newest lab in Gardiner, Maine.</p><p><b>Duties and Responsibilities:</b></p><p>• Analyzing data generated by the laboratory personnel and analytical instruments.</p><p>• Quality control checking of all data generated by the laboratory.</p><p>• Being able to spot outliers and investigate anomalous instances of data.</p><p>• Issues statements of conformity or opinions or interpretations when necessary</p><p>• Work with the laboratory and quality assurance to ensure client complaints or issues are resolved in a timely and professional manner.</p><p>• Interpret analytical data including chromatograms.</p><p>• Input data to database such as LIMS and METRC.</p><p>• Generating and sending reports to various clients.</p><p>• Review and validate data processed by other data analysts</p><p><b>Qualifications:</b></p><p>• Exceptional analytical, organization, problem solving and time management skills.</p><p>• Must be trained on all policies related to data analysis and reporting.</p><p>• Detail-oriented</p><p>• Strong ability to multi-task</p><p>• Ability to handle and analyze large datasets</p><p>• Proficient in MS Office</p><p>• Good communication skills</p><p>• Ability to identify procedural inadequacies or errors and communicate with the department to resolve the issue Requirements</p><p>• Ability to work flexible hours</p><p>• Minimum of BA/BS, with an emphasis on STEM fields with 1 year of experience or 5 years of experience in analytical data processing.</p><p>• Fully understand the navigation of LIMS to assist other departments, including but not limited to Client Service, Scientific Operations, and Laboratory Operations</p><p>• Great familiarity with client specific trends to raise questions on outliers in their samples</p><p>• Must be at least 21 years of age</p><p>• Must be able to pass background check.</p><p>• Advance data analytical skills with Excel</p><p>• Able to work in with a team and independently</p><p>MCR Labs is an equal opportunity employer. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, age, disability, sexual orientation, gender identity, sex, national origin, protected veteran status, or any other basis protected by federal, state, or local law.</p><p>VQQ84RMGM8</p></div>","company":{"companyType":"Private/Growth","name":"MCR Labs","logoUrl":"/logos/mcr-labs-aed09bd7c5f16aa5e7ebc524f087c747.jpeg"},"location":{"country":"United States","address":"United States"},"frontendLink":"/job-posting/mcr-labs/data-analyst/88f6247d4a6c7259101a5084bb3ddc13","title":"Data Analyst","category":"Medical & Healthcare","hash":"88f6247d4a6c7259101a5084bb3ddc13","postingUrl":"https://jobs.laimoon.com/jobs/externalview/29003283"},{"function":["Data & Analytics"],"postedOn":"4 days ago","description":"<div><div><h1>Job Title: Data Analyst</h1><p><br /></p><h2>Company Background:</h2><p>Since 2013 MCR Labs has been your partner in cannabis science. Our team is made up of researchers, chemists, and pharmaceutical scientists, but we’re also enthusiasts, cannasseurs, and members of the cannabis community. We support the community by providing anyone interested in or passionate about cannabis with access to analytical product testing as well as information to help guide their cultivation, consumption, or enjoyment of marijuana, hemp, and cannabis-derived products.</p><p></p><p><br />As the first independent cannabis testing laboratory to be certified by the state of Massachusetts, we are proud to offer analytical testing and R&amp;D services to MMJ and adult-use cannabis providers, patients, doctors, caregivers, or anyone crafting their own cannabis products. Our methods are ISO-17025 accredited, and we employ proven analytical practices developed in the pharmaceutical industry.</p><p><br /></p><p>MCR Labs is always looking for quality candidates to join our team of scientists and administrative personnel. The cannabis industry is one of the fastest growing jobs sectors in the nation, which allows us to consistently hire talented individuals who will develop and grow within our industry!</p><p></p><h2><br />Summary:</h2><p>Data analyst works to ensure all data being generated by the laboratory is accurate and of the highest quality. This position is <b>remote</b> but will work with our newest lab in Gardiner, Maine.</p><p><br /></p><h2>Duties and Responsibilities:</h2><ul><li>Analyzing data generated by the laboratory personnel and analytical instruments.</li><li>Quality control checking of all data generated by the laboratory.</li><li>Being able to spot outliers and investigate anomalous instances of data.</li><li>Issues statements of conformity or opinions or interpretations when necessary</li><li>Work with the laboratory and quality assurance to ensure client complaints or issues are resolved in a timely and professional manner.</li><li>Interpret analytical data including chromatograms.</li><li>Input data to database such as LIMS and METRC.</li><li>Generating and sending reports to various clients.</li><li>Review and validate data processed by other data analysts</li></ul><h2><b></b></h2><h2>Qualifications:</h2><ul><li>Exceptional analytical, organization, problem solving and time management skills.</li><li>Must be trained on all policies related to data analysis and reporting.</li><li>Detail-oriented</li><li>Strong ability to multi-task</li><li>Ability to handle and analyze large datasets</li><li>Proficient in MS Office</li><li>Good communication skills</li><li>Ability to identify procedural inadequacies or errors and communicate with the department to resolve the issue Requirements</li><li>Ability to work flexible hours</li><li>Minimum of BA/BS, with an emphasis on STEM fields with 1 year of experience or 5 years of experience in analytical data processing.</li><li>Fully understand the navigation of LIMS to assist other departments, including but not limited to Client Service, Scientific Operations, and Laboratory Operations</li><li>Great familiarity with client specific trends to raise questions on outliers in their samples</li><li>Must be at least 21 years of age</li><li>Must be able to pass background check.</li><li>Advance data analytical skills with Excel</li><li>Able to work in with a team and independently</li></ul><p></p><p><i><br />MCR Labs is an equal opportunity employer. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, age, disability, sexual orientation, gender identity, sex, national origin, protected veteran status, or any other basis protected by federal, state, or local law.</i></p><p></p><p>VQQ84RMGM8</p></div></div>","company":{"companyType":"Private/Growth","name":"MCR Labs","logoUrl":"/logos/mcr-labs-aed09bd7c5f16aa5e7ebc524f087c747.jpeg"},"location":{"address":"Remote"},"frontendLink":"/job-posting/mcr-labs/data-analyst/da6cd7ddd81689f4431d440e4b22bbd9","title":"Data Analyst","category":"Medical & Healthcare","hash":"da6cd7ddd81689f4431d440e4b22bbd9","postingUrl":"https://www.indeed.com/job/data-analyst-ee095da3744fa33f"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"3 days ago","description":"<div><div><h2><b>The Role</b></h2><div>GTI is seeking a Quality and Compliance Specialist to join our cultivation facility. As a Quality and Compliance Specialist, you will be responsible for executing operational quality and compliance related activities at the facility associated with sampling and inspection of incoming material, in process, and finished products, documentation control, quality event investigation, compliance, and audit. 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. Uses experience and knowledge to influence processes, standards, and plans to improve compliance with internal and external standards.</div><h2><b>Responsibilities</b></h2><ul><li>Establish and perform incoming, in-process, and finished product sampling and inspection.</li><li>Reviews in-process batch documentation, logbooks, test results, and good documentation practices.</li><li>Assist site documentation control system. Ensure harmonization of 1GTI quality system.</li><li>Writes Quality Inspection SOPs and forms, including routing and/or approval of change request packages, as requested.</li><li>Facilitate State regulatory and/or 3rd party site inspections.</li><li>Monitor site's compliance to GTI corporate Quality System.</li><li>Assist in performing weekly internal audit to monitor site's compliance activities to State regulations</li><li>Segregation, control and disposition of non-conforming product.</li><li>Identify, recommend and perform quality training as needed.</li><li>Ensure maintenance and control of production quality records.</li><li>Assist production personnel in the investigation of root causes and corrective action of internal rejects, corrective/preventive action, out of control SPC points, and customer complaints.</li><li>Continually study the existing quality system and make recommendations for improvements.</li><li>Perform improvement projects as identified.</li><li>Collect quality data and report metrics to management.</li><li>Monitors compliance to established Good Manufacturing Practice (GMP) guidance.</li></ul><h2><b>Qualifications</b></h2><ul><li>Associates Degree required</li><li>Prior experience in regulated industry in healthcare, medical devices, pharmaceutical, consumer packaged goods (food), or cannabis is highly desired.</li><li>Highly desirable: FDA, GMP, SQF, and/or HACCP experience.</li><li>Strong experience with product sampling and inspection.</li><li>Ability to follow written procedures and monitor others for adherence to written procedures.</li><li>Ability to create or update written procedures with site operations personnel.</li><li>Strong written and verbal communication skills.</li><li>Strong attention to detail.</li><li>Must understand and comply with the rules, regulations, policies, and procedures of GTI.</li><li>Team player with strong interpersonal skills.</li><li>Open-minded self-starter with the ability to adapt and problem solve, as well manage multiple tasks concurrently.</li><li>Understanding of the Medical Marijuana laws, rules and regulations is preferred and the passion to further their understanding and knowledge of the industry and the laws.</li></ul><h2><b>Additional Requirements</b></h2><ul><li>A self-starter who brings the utmost level of integrity to the company.</li><li>A passion for quality assurance and quality control.</li><li>Must pass any and all required background checks</li><li>Must be and remain compliant with all legal or company regulations for working in the industry</li><li>Must possess valid driver's license</li><li>Must be a minimum of 21 years of age</li><li>Must be approved to receive an Agent badge</li></ul></div><p></p></div>","company":{"companyType":"Private/Established","name":"Green Thumb","logoUrl":"/logos/green-thumb-d605a1142745eee008e37bcb941371b1.jpeg"},"location":{"country":"United States","address":"Holyoke, MA","city":"Holyoke","stateProvince":"MA"},"frontendLink":"/job-posting/green-thumb/quality-and-amp-compliance-technician/fc13fee20336133485c57782b1f2e834","title":"Quality &amp; Compliance Technician","category":"Professional, Scientific, and Technical Services","hash":"fc13fee20336133485c57782b1f2e834","postingUrl":"https://www.indeed.com/job/quality-compliance-technician-929948cb6aef4a9e"},{"salaries":[{"salaryStart":"$46k","salaryEnd":"$110k","currency":"US","source":"Glassdoor","position":"QA Lead","type":"per year","url":"https://www.glassdoor.com/Salaries/portland-qa-lead-salary-SRCH_IL.0,8_IM700_KO9,16.htm"},{"salaryStart":"$66k","salaryEnd":"$110k","currency":"US","source":"Salary.com","position":"Test Lead","type":"per year","url":"https://www.salary.com/research/salary/posting/test-lead-salary/portland-or"},{"salaryStart":"$25k","salaryEnd":"$48k","currency":"US","source":"ZipRecruiter","position":"Quality Assurance Technician","type":"per year","url":"https://www.ziprecruiter.com/Salaries/Quality-Assurance-Technician-Salary-in-Portland,OR"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"7 days ago","description":"<div><p>Phylos is a crop science company using modern molecular genetics and computational biology to breed the next generation of hemp and cannabis. Since 2014 we have supported grower success with genetic testing products offering unparalleled accuracy and reliability. We are a new generation of plant scientists, transforming the hemp and cannabis industries with elite seeds and clones. By leveraging our deep expertise in the cannabis genome, we are unlocking the potential of this plant to be grown at scale, providing cultivators in every region with the varieties, tools, and expertise to drive business growth. POSITION SUMMARY: As the Quality Lead, you will be assisting in all aspects of Quality systems development, execution, and continuous improvement. You will work in collaboration with cross-functional teams to improve and implement processes while meeting regulatory compliance standards and company goals. You are a proactive, solutions oriented thinker and you love finding ways to standardize and improve processes. This position is temporarily remote. RESPONSIBILITIES: Perform analysis of products, deviations, process changes, CAPAs, technology transfers, and other metrics to identify trends and provide recommendations to Quality Management for continuous improvement. Draft, review, approve, and maintain controlled documents, validation plans, change controls, equipment inspections, safety documentation, and scientific reports as needed. Assist in all aspects of Quality Systems development and in program execution and enhancement. Provide direction, motivation, and leadership to the Quality Team as recommended by Quality Management. Assess customer requirements and ensure that these are met. Respond to customer inquiries or complaints as needed. Assist in monitoring/validating current and new internal procedures for accuracy and efficiency. Lead weekly Quality team meetings and provide project updates to Quality management. Schedule, conduct, and analyze findings for internal audits where applicable, to ensure compliance to current SOPs, processes, and/or regulatory requirements. Compile monthly, quarterly, and annual metrics relating to Quality for Quality Management review. Assist with training programs for new employees and maintain training records. Design and provide recurring training on quality procedures and company best practices as needed. Review and suggest new software and tools to reduce waste, facilitate continuous improvement, encourage cross-functional workflows QC all internal software deploys for SIMS to ensure accuracy. Pro-actively encourages continuous improvement and daily problem-solving initiatives to increase operational effectiveness and efficiency. Responsible for organizing and maintaining the testing schedule for Seed Co., certification renewal, and international shipment documentation records. QUALIFICATIONS: BS/BA in Biology, Agriculture, Chemistry and/or other related fields preferred. 3 years of professional experience in Quality Assurance. Knowledge of ISO 9001, ISO 17025, GMP, and GLP preferred. Ability to develop and follow protocols, policies and procedures with exactness. Strong communication and organizational skills with ability to work on multiple priorities at once with high attention to detail. Proven experience in implementing processes in collaboration with cross functional teams. Strong analytical and technical writing skills. Current experience with MS Office, Google Suite, and Smartsheet or similar project management system. Ability to sit and stand for prolonged periods. Ability to perform repetitive motions with hands and arms. Comfortable in a fast-paced environment. Must be a self-starter demonstrating initiative with the ability to work in an independent and organized manner. Working knowledge of Quality systems required. We have been honored to receive inquiries for our positions from all over the world. In order to have the best possible outcome in the hiring process, we would like to make sure that you are aware that: 1. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. 2. Given the current status of cannabis in the US, if you are not a US citizen, there is a possibility that this association may jeopardize the status of your VISA, and/or your ability to exit and reenter the United States. If this is a concern for you, please contact your immigration attorney regarding this potential risk prior to proceeding with your application Monthly updates with the latest news, events, and helpful resources</p></div>","company":{"website":"phylos.bio","name":"Phylos Bioscience, Inc."},"location":{"country":"United States","address":"Portland, OR, USA","city":"Portland","stateProvince":"OR"},"frontendLink":"/job-posting/phylos-bioscience-inc/quality-lead/a3a869c65897833266f7cdd1a99945ac","title":"Quality Lead","category":"Agriculture & Farming","hash":"a3a869c65897833266f7cdd1a99945ac","postingUrl":"https://www.recruit.net/job/quality-lead-jobs/BD739AE6430AC649","salary":"$46k - $110k"},{"salaries":[{"salaryStart":"$32","salaryEnd":"$49","currency":"","source":"ERI Economic Research Institute","position":"Quality Assurance Specialist","type":"per hour","url":"https://www.erieri.com/salary/job/quality-assurance-specialist/canada/ontario/chatham-kent"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"6 days ago","description":"<div><p>Quality Assurance Associate - Processing Leamington ON. Monday-Friday 11 : 00PM-7 : 30AM About Tilray Tilray is a global pioneer in cannabis research, cultivation, processing and distribution currently serving tens of thousands of patients in ten countries spanning five continents.</p><p>Looking to develop your career at the forefront of a rapidly expanding industry? Job Summary : Reporting to the Quality Assurance Supervisor, this position will be responsible for supporting Tilray's Quality Assurance team in the cultivation department.</p><p>As industry leaders committed to offering clean, safe, and pure cannabis products, we engage in a collaborative culture that is fast paced, dynamic and highly motivating.</p><p>If you’re looking to thrive in a new, rapidly growing and innovative space, we would love to hear from you. We are currently seeking a strong leader to join our Quality team.</p><p>This position will be Monday-Friday with some required Saturdays on a rotational swing shift of 6 : 30AM-3 00PM &amp; 3 : 00PM-11 : 30PM.</p><p><b>Your day-to-day responsibilities will consist of :</b></p><p>• Continually monitor processing areas for GPP regulatory requirements under the Cannabis Act and Cannabis Regulations and their associated regulations such as those for Natural Health Products.</p><p>• Assist all functional departments on establishing systems to eliminate GACP / GPP gaps that relate to Processing and manufacturing</p><p>• Support and maintain systems to ensure quality of products as defined through internal Good Production Practices and established Standard Operating Procedures.</p><p>• Communicate, educate and support the quality requirements to all operational departments.</p><p>• Create, review and maintain Standard Operational Procedures, investigate non-conformances / deviations and customer complaints as it relates to quality.</p><p>• Participate in the initiation and writing of change controls to controlled documents as needed to ensure defined quality objectives are met</p><p>• Coordinate and conduct new hire and ongoing GPP / GACP training.</p><p>• Read, understand and follow safe work procedures</p><p>• Other duties as assigned</p><p><b>To be successful in this position you will have the following :</b></p><p>• A combination of bachelor’s degree in science related field and / or technical Diploma from an accredited post-secondary institution.</p><p>• Quality experience in a horticulture, food or health product environment is preferred</p><p>• Knowledge of plant science, pest management, GPP / GACP (Good Production Practices / Good Agricultural and Collection Practices) or GMP (Good manufacturing Practices) would be considered an asset</p><p>• Superior communication and writing skills</p><p>• Self-starter, critical thinker and team oriented</p><p>• High work ethic standards are a must</p><p>• Exceptional attention to detail</p><p>• Candidates must be able to work swing shift hours (two weeks days 6 : 30 am-3 : 00 pm, two weeks afternoons 8 : 30am-5 : 00pm).</p><p>Weekend coverage may be required.</p><p>Due to the nature of the business and working with controlled substances, all new employees will be required to complete a background check prior to starting work.</p><p>This may include : verifying work references, validating all credentials and criminal record checks.</p><p>It is a requirement that the selected Candidate be legally eligible to work in Canada at the time an offer is presented.</p><p>Internal Candidates : For any internal applicants, we ask that you bring a hard copy of your resume with a supporting cover letter to the Human Resources Office, send a direct email to our Talent Acquisition Specialist or apply online at https : / / www.</p><p>tilray.com / careers Note : The statements above are intended to describe the general nature and level of work being performed by people assigned to the job.</p><p>They are not constructed to be an exhaustive list of responsibilities, duties and skills required of personnel in the job.</p><p>Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer.</p><p>Tilray is committed to providing an accessible and barrier-free environment. Please advise Human Resources if you require accommodation during any part of the recruitment process</p></div>","company":{"website":"tilray.com","companyType":"Public/Established","name":"Tilray","logoUrl":"/logos/tilray-7a827f507c4afad3caee3c003054401d.png"},"location":{"country":"Canada","address":"Leamington, ON","city":"Leamington","stateProvince":"ON"},"frontendLink":"/job-posting/tilray/quality-assurance-associate/1016eb997ca610f5e9b1d904c4f6b748","title":"Quality Assurance Associate","category":"Medical & Healthcare","hash":"1016eb997ca610f5e9b1d904c4f6b748","postingUrl":"https://ca.talent.com/view?id=02f198da6b98","salary":"$32 - $49"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"6 days ago","description":"<div><p>Quality Assurance Associate - Processing Leamington ON.</p><p>Monday-Friday 11:00PM-7:30AM</p><p>About Tilray</p><p>Tilray is a global pioneer in cannabis research, cultivation, processing and distribution currently serving tens of thousands of patients in ten countries spanning five continents.</p><p>Looking to develop your career at the forefront of a rapidly expanding industry?</p><p><b>Job Summary:</b></p><p>Reporting to the Quality Assurance Supervisor, this position will be responsible for supporting Tilray's Quality Assurance team in the cultivation department. As industry leaders committed to offering clean, safe, and pure cannabis products, we engage in a collaborative culture that is fast paced, dynamic and highly motivating. If you’re looking to thrive in a new, rapidly growing and innovative space, we would love to hear from you. We are currently seeking a strong leader to join our Quality team. This position will be Monday-Friday with some required Saturdays on a rotational swing shift of 6:30AM-3:00PM 3:00PM-11:30PM.</p><p><b>Your day-to-day responsibilities will consist of:</b></p><p>• Continually monitor processing areas for GPP regulatory requirements under the Cannabis Act and Cannabis Regulations and their associated regulations such as those for Natural Health Products.</p><p>• Assist all functional departments on establishing systems to eliminate GACP/GPP gaps that relate to Processing and manufacturing</p><p>• Support and maintain systems to ensure quality of products as defined through internal Good Production Practices and established Standard Operating Procedures.</p><p>• Communicate, educate and support the quality requirements to all operational departments.</p><p>• Create, review and maintain Standard Operational Procedures, investigate non-conformances/deviations and customer complaints as it relates to quality.</p><p>• Participate in the initiation and writing of change controls to controlled documents as needed to ensure defined quality objectives are met</p><p>• Coordinate and conduct new hire and ongoing GPP/GACP training.</p><p>• Read, understand and follow safe work procedures</p><p>• Other duties as assigned</p><p><b>To be successful in this position you will have the following:</b></p><p>• A combination of bachelor’s degree in science related field and/or technical Diploma from an accredited post-secondary institution.</p><p>• Quality experience in a horticulture, food or health product environment is preferred</p><p>• Knowledge of plant science, pest management, GPP/GACP (Good Production Practices/Good Agricultural and Collection Practices) or GMP (Good manufacturing Practices) would be considered an asset</p><p>• Superior communication and writing skills</p><p>• Self-starter, critical thinker and team oriented</p><p>• High work ethic standards are a must</p><p>• Exceptional attention to detail</p><p>• Candidates must be able to work swing shift hours (two weeks days 6:30 am-3:00 pm, two weeks afternoons 8:30am-5:00pm). Weekend coverage may be required.</p><p>• Due to the nature of the business and working with controlled substances, all new employees will be required to complete a background check prior to starting work. This may include: verifying work references, validating all credentials and criminal record checks.</p><p>• It is a requirement that the selected Candidate be legally eligible to work in Canada at the time an offer is presented.</p><p>Internal Candidates: For any internal applicants, we ask that you bring a hard copy of your resume with a supporting cover letter to the Human Resources Office, send a direct email to our Talent Acquisition Specialist or apply online at https://www.tilray.com/careers</p><p>Note: The statements above are intended to describe the general nature and level of work being performed by people assigned to the job. They are not constructed to be an exhaustive list of responsibilities, duties and skills required of personnel in the job. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer. Tilray is committed to providing an accessible and barrier-free environment. Please advise Human Resources if you require accommodation during any part of the recruitment process</p></div>","company":{"website":"tilray.com","companyType":"Public/Established","name":"Tilray","logoUrl":"/logos/tilray-7a827f507c4afad3caee3c003054401d.png"},"location":{"country":"Canada","address":"Leamington, ON","city":"Leamington","stateProvince":"ON"},"frontendLink":"/job-posting/tilray/quality-assurance-associate-midnights/8142efbc942057795fa065651affcd6a","title":"Quality Assurance Associate (Midnights)","category":"Medical & Healthcare","hash":"8142efbc942057795fa065651affcd6a","postingUrl":"https://www.ziprecruiter.com/c/Tilray/Job/Quality-Assurance-Associate-(Midnights)/-in-Leamington,ON?jid=ec33ec97b92a3af3"},{"employmentType":"Contractor","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"6 days ago","description":"<div><p>Quality Assurance Associate - Processing Leamington ON.</p><p>Monday-Friday 11:00PM-7:30AM</p><p>About Tilray</p><p>Tilray is a global pioneer in cannabis research, cultivation, processing and distribution currently serving tens of thousands of patients in ten countries spanning five continents.</p><p>Looking to develop your career at the forefront of a rapidly expanding industry?</p><p><b>Job Summary</b></p><p>Reporting to the Quality Assurance Supervisor, this position will be responsible for supporting Tilray's Quality Assurance team in the cultivation department. As industry leaders committed to offering clean, safe, and pure cannabis products, we engage in a collaborative culture that is fast paced, dynamic and highly motivating. If you’re looking to thrive in a new, rapidly growing and innovative space, we would love to hear from you. We are currently seeking a strong leader to join our Quality team. This position will be Monday-Friday with some required Saturdays on a rotational swing shift of 6:30AM-3:00PM 3:00PM-11:30PM.</p><p>Your Day-to-day Responsibilities Will Consist Of</p><p>• Continually monitor processing areas for GPP regulatory requirements under the Cannabis Act and Cannabis Regulations and their associated regulations such as those for Natural Health Products.</p><p>• Assist all functional departments on establishing systems to eliminate GACP/GPP gaps that relate to Processing and manufacturing</p><p>• Support and maintain systems to ensure quality of products as defined through internal Good Production Practices and established Standard Operating Procedures.</p><p>• Communicate, educate and support the quality requirements to all operational departments.</p><p>• Create, review and maintain Standard Operational Procedures, investigate non-conformances/deviations and customer complaints as it relates to quality.</p><p>• Participate in the initiation and writing of change controls to controlled documents as needed to ensure defined quality objectives are met</p><p>• Coordinate and conduct new hire and ongoing GPP/GACP training.</p><p>• Read, understand and follow safe work procedures</p><p>• Other duties as assigned</p><p><b>To be successful in this position you will have the following:</b></p><p>• A combination of bachelor’s degree in science related field and/or technical Diploma from an accredited post-secondary institution.</p><p>• Quality experience in a horticulture, food or health product environment is preferred</p><p>• Knowledge of plant science, pest management, GPP/GACP (Good Production Practices/Good Agricultural and Collection Practices) or GMP (Good manufacturing Practices) would be considered an asset</p><p>• Superior communication and writing skills</p><p>• Self-starter, critical thinker and team oriented</p><p>• High work ethic standards are a must</p><p>• Exceptional attention to detail</p><p>• Candidates must be able to work swing shift hours (two weeks days 6:30 am-3:00 pm, two weeks afternoons 8:30am-5:00pm). Weekend coverage may be required.</p><p>• Due to the nature of the business and working with controlled substances, all new employees will be required to complete a background check prior to starting work. This may include: verifying work references, validating all credentials and criminal record checks.</p><p>• It is a requirement that the selected Candidate be legally eligible to work in Canada at the time an offer is presented.</p><p>Internal Candidates: For any internal applicants, we ask that you bring a hard copy of your resume with a supporting cover letter to the Human Resources Office, send a direct email to our Talent Acquisition Specialist or apply online at https://www.tilray.com/careers</p><p>Note: The statements above are intended to describe the general nature and level of work being performed by people assigned to the job. They are not constructed to be an exhaustive list of responsibilities, duties and skills required of personnel in the job. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer. Tilray is committed to providing an accessible and barrier-free environment. Please advise Human Resources if you require accommodation during any part of the recruitment process</p></div>","company":{"website":"tilray.com","companyType":"Public/Established","name":"Tilray","logoUrl":"/logos/tilray-7a827f507c4afad3caee3c003054401d.png"},"location":{"country":"Canada","address":"Staples, ON","city":"Staples","stateProvince":"ON"},"frontendLink":"/job-posting/tilray/quality-assurance-associate-midnights/732dde43e13843fde509843580486f38","title":"Quality Assurance Associate (Midnights)","category":"Medical & Healthcare","hash":"732dde43e13843fde509843580486f38","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-associate-midnights-at-tilray-2766129149"},{"salaries":[{"salaryStart":"$21k","salaryEnd":"$99k","currency":"US","source":"ZipRecruiter","position":"Business Analyst Internship","type":"per year","url":"https://www.ziprecruiter.com/Salaries/Business-Analyst-Internship-Salary--in-Florida"},{"salaryStart":"$42k","salaryEnd":"$94k","currency":"US","source":"Glassdoor","position":"Data Analyst","type":"per year","url":"https://www.glassdoor.com/Salaries/miami-data-analyst-salary-SRCH_IL.0,5_IC1154170_KO6,18.htm"}],"employmentType":"Internship","function":["Data & Analytics"],"postedOn":"5 days ago","description":"<div><p>Business Analyst Intern</p><p><b>Job Description</b></p><p>Springbig is the leading SaaS marketing technology platform serving retailers and brands in the rapidly growing cannabis industry throughout the U.S.</p><p>and Canada.</p><p>We serve in excess of 1,000 clients across 2,300 locations and our clients communications using the Springbig platform access more than 37 million consumers making Springbig the leading company in our sector.</p><p>We have been ranked in the top 100 fastest growing companies in the prestigious Inc.5000 list for two consecutive years, ranking 69th in the recently released 2021 list.</p><p>Springbig recently launched a new platform, Brands by Springbig.</p><p>This is also a SaaS platform, and it allows cannabis brands to collaborate with our dispensary clients to send engaging SMS campaigns to the dispensarys database of consumers.</p><p>A brand can use this platform to place an advertisement on top of hundreds of thousands of text messages and drive their products sell-through like never before This gives brands direct access to consumers in a way theyve never had before and an unprecedented reporting on campaign attribution.</p><p>Our headquarters are in Boca Raton, FL where the majority of our 160 employees are located, and we have additional office locations in Seattle, WA and Toronto, Canada.</p><p><b>Position Overview:</b></p><p>As a Business Analyst Intern at our company, you will be responsible for providing support and collaborating across departments.</p><p>Youll wear multiple hats, turn ambiguity into details, and continuously find opportunities to improve performance and increase reliability.</p><p><b>Minimum Qualifications:</b></p><p>Junior or senior level student enrolled in an accredited university and pursuing a graduate or undergraduate degree. Non-STEM students are encouraged to apply Minimum 3.0 GPA on a 4.0 scale.</p><p><b>Demonstrated knowledge in one or more of the following technologies:</b></p><p>SQL, Jira, Confluence, Tableu, PostgreSQL, and are an eager learner. Strong foundation in technology, leadership, problem solving, analytical thinking, and multi- tasking abilities. Good verbal and written communication skills.</p><p><b>Roles and Responsibilities:</b></p><p>Provide support and work closely with the team to acquire a deep understanding of the features and product and to identify gaps and other missing details.</p><p>Cooperate, collaborate, and strive to specify consistency of the user experience in order to optimize customers interaction with our software.</p><p>Assist with concepts as input, develop and document detailed specifications for implementation of complex features and products. Assist with generating specifications that are complete, easy to understand, and estimate by both the Development and QA Teams. Develop and continually improve Springbigs standards for requirements, specifications, and test plans. Participate in the final feature and product acceptance to make sure that they were built as specified.</p><p><b>Our current stack:</b></p><p>Rails 6 rspec sidekiq</p></div>","company":{"website":"springbig.com","companyType":"Private/Growth","name":"springbig","logoUrl":"/logos/springbig-ece1da006b5db2789f59c7e97e45f937.jpeg"},"location":{"country":"United States","address":"Boca Raton, FL, USA","city":"Boca Raton","stateProvince":"FL"},"frontendLink":"/job-posting/springbig/business-analyst-intern/082077144ca70a6b05bbc865267ce494","title":"Business Analyst Intern","category":"Information Technology & Services","hash":"082077144ca70a6b05bbc865267ce494","postingUrl":"https://us.bebee.com/job/20211020-9975afc185749139dff185052921bdf7","salary":"$21k - $99k"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"4 days ago","description":"<div><div><h2><b>The Role</b></h2><div>The purpose of this position is to ensure the successful quality and compliance management operations at our Oglesby, IL cultivation facility. This position will play a key role in developing, implementing, and upgrading quality assurance policies and standard operating procedures, as well as compliance, development, and implementation of HACCP programs, product quality tracking systems, FDA standards, ingredient management programs, allergen and sanitization management programs, product safety practices, internal and external audits, etc. This position will also ensure compliance with all GTI corporate operating procedures, as well as applicable federal, state, county, and municipal laws, regulations, ordinances, and regulations.</div><h2><b>Responsibilities</b></h2><ul><li>Supports the Quality Department and ensure all employees understand and follow all standard operating procedures (SOPs)</li><li>Define, implement, and improve the Quality Management System including development of process and product testing to ensure quality standards are met and oversee determination of finished product disposition</li><li>Partner with management to lead quality initiatives that develop and maintain a high performing, scalable, and compliant quality system</li><li>Implement, maintain, and audit sanitation and quality control practices that ensure the safety and quality of cannabis including purity and consistency</li><li>Implement HACCP, allergen, and sanitization management programs</li><li>Review and approve decisions about whether to investigate a cannabis product complaint and review and approve the findings and follow-up action of any investigation performed</li><li>Perform or oversee routine audits of compliance processes to assure accuracy and thoroughness of completion</li><li>Participate in State regulatory compliance inspections, investigate and resolve compliance concerns, issues, or violations</li><li>Analyze facility trends to assess potential areas of continued non-compliance</li><li>Publish monthly metrics focused on facility current QA/QC progress</li><li>Routinely reviews monthly corporate QA/QC documentation and assures that all areas of concern are addressed appropriately according to corporate policy and regulatory standards</li><li>Write Quality SOPs or other standards as necessary</li><li>Promote awareness and responsibility through training and regular communication throughout the facility</li><li>Fosters a high-performance culture through active leadership and create a strong sense of accountability within the Quality Department</li><li>Perform assigned Quality Inspections</li><li>Expected to adhere to safe work practices, follow GMP and HACCP guidelines, maintain sanitary conditions and ensure that product quality is maintained. Report to management any conditions or practices that may adversely affect product safety, product quality or personnel safety</li><li>Maintain a positive work atmosphere by acting and communicating in a manner so that you get along with customers, clients, co-workers and management</li><li>May make decisions and perform the job responsibilities of the Quality &amp; Compliance Manager in their absence</li></ul><h2><b>Qualifications</b></h2><ul><li>Associate degree in Food Science, Biology, Chemistry, or a related field required, Bachelor's Degree in Food Science, Biology, Chemistry, or a related field preferred</li><li>3+ years of regulatory compliance management including interfacing with regulators and inspectors</li><li>5+ years work experience with a proven track record of building and developing QA/QC processes and systems</li><li>Must have the knowledge and skills required to work in a fast paced and challenging environment</li><li>Must be able to work variable day shifts dependent on business need</li><li>Knowledge of the GMP, HACCP and Environmental sanitation programs</li><li>Experience with SQF, ISO, GMP, ASQ, HACCP, PCQI or similar certification experience preferred</li><li>QMS auditor or similar certification preferred</li><li>Possess a strong knowledge of sanitary design, specification, and implementation of food\\pharmaceutical processing systems</li><li>Ability to deliver specific organizational goals and effectively develop, grow, and manage a diverse multisite team to achieve objectives</li><li>Track record of engaging teams and creating a collaborative culture</li><li>Excellent verbal, written and presentation skills</li><li>Exceptional computer skills in Microsoft® Office Suite (Access, Excel, Outlook, PowerPoint, Publisher, Word)</li><li>Strong detail-oriented and resourceful mindset</li></ul><h2><b>Additional Requirements</b></h2><ul><li>Must pass any and all required background checks</li><li>Must be and remain compliant with all legal or company regulations for working in the industry</li><li>Must possess valid driver's license</li><li>Must be a minimum of 21 years of age</li><li>Must be approved to receive an Agent badge</li></ul></div></div>","company":{"companyType":"Private/Established","name":"Green Thumb","logoUrl":"/logos/green-thumb-d605a1142745eee008e37bcb941371b1.jpeg"},"location":{"country":"United States","address":"Oglesby, IL","city":"Oglesby","stateProvince":"IL"},"frontendLink":"/job-posting/green-thumb/quality-and-amp-compliance-technician/0daf1a352aec9c97d4c91293d7710f28","title":"Quality &amp; Compliance Technician","category":"Professional, Scientific, and Technical Services","hash":"0daf1a352aec9c97d4c91293d7710f28","postingUrl":"https://www.indeed.com/job/quality-compliance-technician-440ad78cf410f95c"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"5 days ago","description":"<div><p>Our Client specializes in manufacturing cannabis pre-rolls in their facility in GTA West. The Quality Assurance Specialist (Health Canada Security Clearance) supports operations through the implementation and management of quality systems. They are responsible for ensuring the cannabis products produced meet the organization's objectives for quality, safety, regulatory, and customer expectations in accordance with the Cannabis Act &amp; relevant regulations.</p><p>• *Note: This position requires an active Health Canada Security Clearance.**</p><p><b>Responsibilities:</b></p><p>• Work closely with the Production Manager to oversee the site QA and assist in developing, reviewing, and maintaining SOPs, Quality Management Programs, and projects to ensure compliance under the Cannabis Act/Regulations.</p><p>• Manage production records and labeling records.</p><p>• Work cross-departmentally to implement &amp; maintain SOPs (i.e. Operations, Regulatory, Security).</p><p>• Perform record-keeping tasks and document updates.</p><p>• Collect and review production Quality documents.</p><p>• Perform review, inspection, and/or validation of new materials and equipment.</p><p>• Support release of products through batch record compilation and review.</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>Qualifications:</b></p><p>• Valid security clearance (ACMPR or Cannabis Regulations) is a strong requirement.</p><p>• BSc Degree in Chemistry, Biology, Pharmacology, or Food Science, obtained or recognized by a Canadian University.</p><p>• 4+ years experience in Quality Assurance/Control in a production environment.</p><p>• Previous Cannabis Industry experience preferred.</p><p>• Preferred knowledge of plant chemistry, extraction and formulation systems, and chromatographic techniques.</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></div>","company":{"companyType":"Private/Startup","name":"Cannabis At Work","logoUrl":"/logos/cannabis-at-work-8ae63b190226a7031617f4393f916a20.jpeg"},"location":{"country":"Canada","address":"Regional Municipality of Durham, ON","city":"Regional Municipality Of Durham","stateProvince":"ON"},"frontendLink":"/job-posting/cannabis-at-work/quality-assurance-specialist-health-canada-security-clearance/135e7b4c7109208f437e51863798f4eb","title":"Quality Assurance Specialist (Health Canada Security Clearance)","category":"Professional, Scientific, and Technical Services","hash":"135e7b4c7109208f437e51863798f4eb","postingUrl":"https://www.adzuna.ca/details/2564180142"},{"salaries":[{"salaryStart":"$90k","salaryEnd":"$160k","currency":"US","source":"ZipRecruiter","position":"Remote Data Engineer","type":"per year","url":"https://www.ziprecruiter.com/Salaries/Remote-Data-Engineer-Salary-in-Irvine,CA"}],"employmentType":"Full-time","function":["Engineering","Data & Analytics"],"postedOn":"12 days ago","description":"<div><p>Overview:Weedmaps’ mission is to power a transparent and inclusive global cannabis economy. Through our industry-leading marketplace, we connect the cannabis market’s highest value and intent consumers with the best dispensaries and brands in the world and provide cannabis retailers with the suite of operational tools they need to efficiently run their businesses.Weedmaps is looking for a Data Engineer to help architect, design, build and maintain our data platform. You'll be joining our Data Engineering team where you'll play a key role in driving engineering excellence in support of our business goals.The impact you'll make: Develop and maintain ETL data pipelines, integrating a wide range of data sources to support business applications and internal analytics needs. Create repeatable solution patterns and standards for relevant data management capabilities to ensure data consistency and accuracy, while maintaining SLA requirements.Perform technology and product assessments to drive required infrastructure needs to meet scalability, availability, security and concurrency needs.Cross team collaboration with Product, Analytics and Engineering teams, participate in all phases of SDLC - product requirement gathering, design, development and support. What you've accomplished: 3+ years of Data/Software EngineeringStrong knowledge of data warehousing and data modeling concepts.Experience building data integration pipelines, familiarity with ETL, ELT, Change Data Capture (CDC), Streaming and other data processing patterns.Experience with Airflow or similar workflow management solutions.Coding proficiency in at least one modern programming language, Python preferred.Experience with AWS, good understanding of data services offered and ability to recommend cost effective solutions in and out of the boxStrong knowledge of various relational and non-relational database systems, proficiency at least with one (Postgres, ElasticSearch, Redshift, MongoDB, etc), experience with structured and semi structured data.Experience with streams and event driven patterns is a plus.Excellent documentation and communication skills. Bonus Points: Snowflake Data Warehouse experienceStreamSets or experience with other major ETL tools Our Benefits: 100% paid employee monthly Medical, Dental and Vision premiums AND 80% paid dependent monthly premiums HMO (California residents only) and PPO option offered through United Healthcare Company-paid $50,000 in Basic Life/AD&amp;D (Accidental Death and Dismemberment) coverage401(k) Retirement Plan: 100% match on the first 1%. 50% match from 2-6% of employee contributions3 weeks PTO (accrued) and 5 sick days (immediate)Supplemental, voluntary benefits Kindbody (family planning/fertility) including up to $10,000 towards cash-pay servicesGoodly (Student Loan Repayment/529 Education Savings) including a company contribution of up to $1,000/year Flexible Spending Accounts (Medical, Dependent, Transit and Parking)Voluntary Life InsuranceCritical IllnessAccident InsuranceShort- and long-term disabilityPet Insurance Paid parental leaveDuring current work-from-home: Reimbursements for home office setup and monthly WiFi Our Culture: 11 company-paid holidaysCatered lunch and snacks provided when working in the office Snack boxes sent straight to your door when you work-from-home Casual work environment, read no fancy clothes required, but you are free to dress to the nines!Monthly virtual happy hoursQuarterly all-hands meetings</p></div>","company":{"website":"weedmaps.com","companyType":"Private/Established","name":"Weedmaps","logoUrl":"/logos/weedmaps-91e1d872260508afeaf6f1955f0ae1bf.jpeg"},"location":{"country":"United States","address":"Irvine, CA, USA","city":"Irvine","stateProvince":"CA"},"frontendLink":"/job-posting/weedmaps/data-engineer-remote/fd5e5dcdd9fc1c53aa5d60073ab3d920","title":"Data Engineer (Remote)","category":"Information Technology & Services","hash":"fd5e5dcdd9fc1c53aa5d60073ab3d920","postingUrl":"https://b-jobz.com/us/web/jobposting/10d311e45239","salary":"$90k - $160k"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"6 days ago","description":"<div><p>Our Client has a licensed processing facility in Dauphin, Manitoba, and has a focus on extraction from industrial hemp. The Quality Assurance Person (Health Canada Security Clearance) will ensure that the product produced meets the company's objectives for purity, quality, and security. The Quality Assurance Person must have the ability to meet both external and internal regulatory requirements including legal compliance and customer expectations. The Quality Assurance Person is accountable for the ongoing monitoring of the quality assurance and control systems in compliance with Health Canada Regulations.</p><p>• *Note: This position requires an active Health Canada Security Clearance.**</p><p><b>Responsibilities:</b></p><p>• Ensures that all processing activities are carried out as per Standard Operating Procedures (SOP), at all times.</p><p>• Collaborate with other relevant departments such as operations and marketing to ensure compliance with Health Canada regulations and guidelines.</p><p>• Must ensure that all technical documents at the site in use are current. All the master documents such as site policy documents and Standard Operating Procedures (SOP) must be controlled and secured in accordance with Good Documentation Practices.</p><p>• Review quality agreements with 3rd party customers/external vendors to ensure compliance.</p><p>• Responsible for managing and coordinating staff, creating department efficiencies, and providing leadership support.</p><p>• Must be able to communicate effectively to all levels of management.</p><p>• Managing quality standards, methods, and procedures for inspecting, testing, and evaluating the precision, accuracy, and reliability of company products.</p><p>• Responsible for managing compliance of manufacturing and production processes with internal and external safety, quality, and regulatory standards/requirements for worldwide distributions.</p><p>• Assures compliance to in-house and/or external specifications and standards, such as GMP, GGP, GPP, GDP, ACMPR, etc.</p><p>• Designs methods and procedures for inspecting testing and evaluating the precision and accuracy of production processes, production equipment, and finished products.</p><p>• Performs internal audits, and vendor evaluation audits on a regular basis to determine quality qualifications. Actively participates in external audits such as Health Canada Inspections.</p><p>• Performs analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary.</p><p>• Assists product support areas in gathering and analyzing data.</p><p>• Participates in the reviewing of engineering designs to contribute quality requirements and considerations.</p><p>• Other duties as assigned by Leadership.</p><p><b>Core Competencies:</b></p><p>• Working experience as a Quality Assurance Manager in a cGMP, HACCP, GAP regulated environment with proficiency in documentation and analytical testing.</p><p>• Strong leadership qualities, ability to liaise with internal and external departments.</p><p><b>Qualifications:</b></p><p>• BSc in Biological Sciences/ Pharmacy/ Food (preferred) or post-secondary diploma in Science-related technical discipline.</p><p>• Previous Health Canada Security Clearance and work experience with a Canadian Licensed Producer (LP) is considered as an asset.</p><p>• 5 or more years of experience in Quality Assurance/ Quality Control Department as a supervisor or manager position.</p><p>• Previous experience with inspecting methods in the design, fabrication, and production of medical cannabis is an asset.</p><p>• Previous experience operating in a fast-paced organizational environment.</p><p>• Demonstrated project planning and management capabilities; experience with change management.</p><p>• Previous experience as stand-alone QA/QC resource; direct responsibility for determining the strategy to meet quality objectives with the available resources as well as tactical execution</p></div>","company":{"companyType":"Private/Startup","name":"Cannabis At Work","logoUrl":"/logos/cannabis-at-work-8ae63b190226a7031617f4393f916a20.jpeg"},"location":{"country":"Canada","address":"Dauphin, MB","city":"Dauphin","stateProvince":"MB"},"frontendLink":"/job-posting/cannabis-at-work/quality-assurance-person-health-canada-security-clearance/3399542dd3eaf491421122f63fba9991","title":"Quality Assurance Person (Health Canada Security Clearance)","category":"Professional, Scientific, and Technical Services","hash":"3399542dd3eaf491421122f63fba9991","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-person-health-canada-security-clearance-at-cannabis-at-work-2755975572"},{"employmentType":"Full-time","function":["Data & Analytics"],"postedOn":"5 days ago","description":"<div><p>Lyonleaf is home to some of the most innovative, caring, and passionate employees in the cannabis industry. Together, we form a united front to advance our goal of closing the gap in patients’ needs for standardized medical cannabis.</p><p>Lyonleaf’s mission is to elevate the medicinal value of cannabis, through data and science, to consistently serve our patients. The three pillars that guide all our decisions are that we are patient centric, scientific, and caring about employee wellness.</p><p>If you are looking for an opportunity where you can truly make a difference in bettering people’s lives, we want to hear from you.</p><p>Reporting to our Product Analyst, we are looking for a detail-oriented team player to join our Business Intelligence department as our<i><b> Data Collection Technician</b></i> responsible for collecting all cultivation data.</p><p>WHAT WILL YOUR DAYS LOOK LIKE?</p><ul><li>Working in cannabis production rooms gathering various sets of data: morphology, lab samples, light readings, and more.</li></ul><ul><li>Collect, validate, and enter data into our online database, and report any discrepancies.</li></ul><ul><li>Daily reports to our Product Analyst.</li></ul><ul><li>Strict adherence to procedures and practices according to SOP’s.</li></ul><ul><li>Maintain concise daily records and ensure documentation is accessible and organized in compliance with company SOPs and Health Canada regulations.</li></ul><ul><li>Working hours are 10:00am-6:00pm.</li></ul><ul><li>Other duties as assigned.</li></ul><p>WHAT WILL YOU BRING TO THE TABLE?</p><ul><li>High School Diploma</li></ul><ul><li>1+ years experience in data entry, agriculture, or another similar role.</li></ul><ul><li>Experience using pH meters, PAR meters, anemometers, IR sensors, etc.</li></ul><ul><li>Passionate about data, science, and cannabis.</li></ul><ul><li>Excellent organizational and time management skills.</li></ul><ul><li>Team player and excellent independent worker.</li></ul><ul><li>Attention to detail is imperative to success in this role.</li></ul><ul><li>Ability to complete repetitive tasks in a timely manner.</li></ul><ul><li>Strong technology and computer skills: Microsoft Excel and database entry.</li></ul><ul><li>Additional experience in data analytics, SQL, Tableau, etc. is an asset.</li></ul><ul><li>Experience in a Health Canada licensed cannabis production facility is an asset.</li></ul><p>Job Type: Full-time</p><p>Salary: $16.00-$18.00 per hour</p><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Experience:</p><ul><li>Data Entry: 1 year (preferred)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"LyonLeaf","logoUrl":"/logos/lyonleaf-cannabis-inc-3846e7594816b1e11802eddc2b590a3b.png"},"location":{"country":"Canada","address":"Montréal, QC","city":"MontréAl","stateProvince":"QC"},"frontendLink":"/job-posting/lyonleaf/data-collection/72d22db6f551d2c2b6a5353a35e88878","title":"Data collection","category":"Medical & Healthcare","hash":"72d22db6f551d2c2b6a5353a35e88878","postingUrl":"https://ca.indeed.com/job/data-collection-34810bf4093cabcf"},{"function":["Legal"],"postedOn":"2 days ago","description":"<div><div><h2><b>The Role</b></h2><p>As a Licensing Specialist at Green Thumb Industries Inc., you will be responsible for drafting and submitting license renewal applications across the business as well as tracking all operational licenses across the business. You will collaborate with the compliance and legal teams, as well as cross-functionally, on all projects related to licensing. Our ideal candidate is one with applicable experience in licensing who is comfortable working with ambiguity and invigorated by the challenge of licensing in a new and highly regulated industry!</p><h2><b>Responsibilities</b></h2><ul><li>Initiate operational license renewals and organize materials for submission to state regulatory agencies</li><li>Track operational license renewals post-submission and process monthly status report for senior staff</li><li>Provide physical copies of operational licenses and operational license-related data for vendor requests and new market application submissions</li><li>Notify regulatory agencies of ownership changes</li><li>Maintain an up-to-date database and records of all state operational licenses/permits for all retail and wholesale facilities</li><li>Maintain an up-to-date/secure database of all principal officer and entity data for licensing purposes</li><li>Ensure facilities receive all operational licenses in a timely manner to post on-site</li><li>Work with outside counsel as needed, for operational license renewals, principal officer registrations, M&amp;A, and ownership updates</li><li>Distribute regulator inquiries to appropriate internal points of contact, gather responses and submit back to regulators accordingly</li><li>Participate in cross-departmental projects and provide expertise on all things related to operational licenses as needed</li><li>Additional roles and responsibilities as assigned</li></ul><h2><b>Qualifications</b></h2><ul><li>4+ years experience in licensing, highly regulated industry experience preferred</li><li>A minimum of 2 years in cannabis industry preferred</li><li>Bachelors degree or equivalent work experience required</li><li>Paralegal certification preferred</li><li>Notary of the public preferred</li><li>Highly motivated, self-directed, innovative and able to work independently or among teams with keen judgement, common sense and resourcefulness</li><li>Comfortable working with a degree of ambiguity</li><li> Adapts and thrives in a demanding, fast-paced environment</li><li>Operates with a high level of professionalism and integrity, including dealing with confidential information</li><li>Must have a solid understanding of the laws, rules and regulations applicable to the cannabis industry and passion to further your understanding and knowledge of the industry and the laws</li></ul><h2><b>Additional Requirements</b></h2><ul><li>Must pass any and all required background checks</li><li>Must be and remain compliant with all legal or company regulations for working in the industry</li><li>Must possess valid driver's license</li><li>Must be a minimum of 21 years of age</li><li>Must be approved by state badging agency to work in cannabis industry</li></ul></div></div>","company":{"companyType":"Private/Established","name":"Green Thumb","logoUrl":"/logos/green-thumb-d605a1142745eee008e37bcb941371b1.jpeg"},"location":{"country":"United States","address":"Chicago, IL","city":"Chicago","stateProvince":"IL"},"frontendLink":"/job-posting/green-thumb/compliance-specialist-licensing/ea2d9b0b746aa3aad61c20dc61abb24e","title":"Compliance Specialist, Licensing","category":"Professional, Scientific, and Technical Services","hash":"ea2d9b0b746aa3aad61c20dc61abb24e","postingUrl":"https://www.indeed.com/job/compliance-specialist-licensing-e8f621b9253d3c62"},{"salaries":[{"salaryStart":"$57k","salaryEnd":"$93k","currency":"","source":"PayScale","position":"Software Quality Assurance (SQA) Lead Tester","type":"per year","url":"https://www.payscale.com/research/CA/Job=Software_Quality_Assurance_(SQA)_Lead_Tester/Salary/8242f4ef/Toronto-ON"},{"salaryStart":"$50k","salaryEnd":"$63k","currency":"","source":"Glassdoor","position":"QA Analyst","type":"per year","url":"https://www.glassdoor.ca/Salary/LifeWorks-QA-Analyst-Toronto-Salaries-EJI_IE443726.0,9_KO10,20_IL.21,28_IM976.htm"},{"salaryStart":"$46","salaryEnd":"$73","currency":"","source":"ERI Economic Research Institute","position":"Quality Assurance Manager","type":"per hour","url":"https://www.erieri.com/salary/job/quality-assurance-manager/canada/ontario/burlington"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"9 days ago","description":"<div><p>Quality Assurance Person (QAP) Location: Bradford, ON Overview: Reporting to the Manager, Quality Assurance the Quality Assurance Person is responsible for Good Production Practices (GPP) according to Health Canada and Good Manufacturing Practices within the corporate Quality Management System (QMS). Integrate, over-see, maintain, and report actual conformance status in the following areas: GMP, GPP Compliance, Training and Awareness Batch Release, both Domestic and International Internal Audit Program QAP Task Transfer Monitoring Recall Program Pest Control Program Clinical Trials Preventive Control Plan, as assigned Product Development and/or Operations Trials, as assigned Provide technical guidance and oversight in partnership with the Quality Assurance Manager in the following areas: Product Compliance External Audits Annual Product Quality Review Preventive Control Plans Quality Risk Management Product Non-conformance or OOS Primary Job Responsibilities: Assess, interpret, and ensure compliance with applicable regulations and/or other governing bodies Assess cannabis and controlled material test methods to ensure compliance for intended market Inform Quality Manager and/or Department of critical regulatory changes, or potential gaps Co-lead Health Canada and/or other external audits in partnership with QAM Provide technical directive and decision making in partnership with the QAM Review and approval of all controlled documents related to product/process Assure the release of Cannabis Products according to SOPs for all markets Collaborate with Quality Assurance Specialist as needed to ensure effective Stability program Support product recall in conjunction with Quality Assurance, Control, and other stakeholders Review Pest Control Reports Monthly review and sign-off of complaints Sign-off of NCR or CAPA with direct impact to Product Quality Sign-off complaints, non-conformances, CAPAs, pest control reports, changes related to GPP etc., Stays up to date on technical Quality Assurance practices within the industry and abroad Maintain security and confidentiality of all aspects of the business Adhere to Aurora SOPs and comply with Health Canada Cannabis Act and EU GMP as applicable Other duties as required Job Requirements: Bachelor’s, Master’s Degree in Science, Pharmacology, Medical Laboratory and/or combined work experience. Security cleared individual according to Canadian Cannabis Act and regulations Currently or previously a Health Canada approved Quality Assurance Person or Alternate Quality Assurance Person (considered an asset) A minimum three to five years of quality assurance experience preferred, preferred technical quality with experience releasing batches Keeps up with scientific knowledge, compliance and industry demands Demonstrated ability to work with others as a member of a team. Knowledge of health and safety standards and compliance. Strong communication and interpersonal skills required to communicate with the department supervisors and workers to insure seamless and transparent evaluation of in-process data and operations. Demonstrated ability to understand and execute verbal and written instructions. Proficiency to prioritize activities. Demonstrated problem solving skills and attention to detail. Capability to maintain both physical and mental fitness and alertness. Position requires ability to work at various levels of height and move freely and independently throughout all areas and levels of the building (including climbing stairs) to work in areas of production, labs, offices and others as required. We would like to thank all applications for their interest but only those selected for an interview will be contacted. Aurora is an equal opportunity employer. At Aurora, we are committed to do business inclusively and accommodate applicants with disabilities. If you require accommodation (including, but not limited to, an accessible interview site, alternate format of job posting) during the recruitment and selection process, please let our Recruitment team know</p></div>","company":{"website":"auroramj.com","companyType":"Public/Established","name":"Aurora Cannabis","logoUrl":"/logos/aurora-cannabis-5846417b31dc1080e3c3b4583c3f2096.png"},"location":{"country":"Canada","address":"Bradford West Gwillimbury, ON","city":"Bradford West Gwillimbury","stateProvince":"ON"},"frontendLink":"/job-posting/aurora-cannabis/quality-assurance-person/e84bcc392d67c304d2c23882e04d632c","title":"Quality Assurance Person","category":"Medical & Healthcare","hash":"e84bcc392d67c304d2c23882e04d632c","postingUrl":"https://www.rapidinterviews.com/job/quality-assurance-person-with-aurora-cannabis-in-bradford-west-gwillimbury-tal-0307","salary":"$57k - $93k"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"9 days ago","description":"<div><p><b>Technician, Quality Assurance - Fenwick</b></p><p><b>Who We Are</b><br />Winner of 7 Canadian Cannabis Awards - Including Best Licensed Producer 2018! This quite possibly is the best company to work for in the world!<br />CannTrust - a front-runner in the cannabis industry, is a federally regulated licensed producer, publicly traded, and a proudly Canadian company. CannTrust is leading the Canadian and global market in producing standardized cannabis products. CannTrust is ready for Cannabis 2.0 and is currently developing new products that span the medical, recreational, beauty, wellness, and pet markets.<br />CannTrust is committed to research and innovation, as well as contributing to the growing body of evidence-based research regarding the use and efficacy of cannabis. Its product development teams along with its global pharma partner, are diligently innovating and developing products that will make it easier for patients to use medical cannabis. CannTrust supports ongoing patient education about medical cannabis and has a compassionate use program to support patients with financial needs.</p><p><b>Who You Are</b><br />The ideal candidate is an agile, business savvy individual who is committed to getting better everyday. You are a passionate influencer with strong communication skills, who is open to giving and receiving feedback. You are customer-centric with an ability to act as a mentor amongst your peers. Of course, you also deliver consistent results by aligning yourself with CannTrust values.</p><p><b>Roles &amp; Responsibilities</b></p><ul><li>Ensure quality and compliance processes within Grow areas, Harvest, Dry/Cure rooms, Manual Groom area, production, and packaging of dried Cannabis</li></ul><ul><li>Support to manage day-to-day operations in compliance with CannTrust quality system requirements and Good Manufacturing Practices and support the implementation of process efficiencies.</li></ul><ul><li>Ensure through shop floor presence and knowledge transfer, that there is in-depth GMP understanding as it pertains to operations and that issues are identified and dealt with through close contact with cross-functional departments</li></ul><ul><li>Perform shop floor process walkabouts and facilities shop floor walkabouts; support operations to remediate issues that are identified</li></ul><ul><li>Perform batch record review in real time on the shop floor</li></ul><ul><li>Perform spot checks, sampling, line clearance, sanitation verification and in process testing</li></ul><ul><li>Assist with deviation and out of specification investigations, corrective and preventative actions, and change controls as required</li></ul><ul><li>Ensure inspection/audit readiness at all times and contribute to GMP inspections and follow up correspondence</li></ul><ul><li>Perform audits in conjunction with the Internal Auditor</li></ul><ul><li>Support operational activities as related to, examples:</li></ul><ul><li>Trouble shooting quality issues</li></ul><ul><li>Make recommendations to improve efficiencies and productivity</li></ul><p><b>Individual Influencer</b></p><ul><li>Customer-centric – always searching for ways to improve service, takes action to resolve (internal or external) customer issues.</li></ul><ul><li>Acts as a mentor to peers and cross functional partners.</li></ul><ul><li>Follows through on commitments, adheres to deadlines.</li></ul><ul><li>Uses good judgment about when to act independently or escalate an issue.</li></ul><ul><li>Acts with Integrity: Demonstrates responsible, ethical, and honest behavior while consistently leading by example.</li></ul><ul><li>Motivates operations to take timely action, and works to resolve escalations in a timely manner</li></ul><ul><li>Monitors progress to departmental goals with company strategy</li></ul><ul><li>Supports achievement of department goals &amp; objectives</li></ul><ul><li>Complies with all company policies</li></ul><ul><li>Delivers results while staying aligned with CannTrust Values.</li></ul><p><b>Education &amp; Experience</b></p><ul><li>B.Sc. in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Engineering (or related field).</li></ul><ul><li>Minimum 3 - 5 years’ experience in quality assurance or related area within the pharmaceutical, healthcare or food/beverage industry.</li></ul><ul><li>Experience in manufacturing operations, laboratory operations, document control, and quality management systems (deviation, CAPA, change control, batch record review).</li></ul><ul><li>Understanding of equipment, manufacturing processes, maintenance, and quality standards.</li></ul><ul><li>Demonstrated and thorough knowledge of GMP relative to Health Canada, FDA, and other global regulations.</li></ul><ul><li>Knowledge of ACMPR, ISO, HACCP, GFSI, or other quality systems is an asset.</li></ul><p><b>Requirements</b></p><ul><li>Ability to influence without authority</li></ul><ul><li>Proficiency in Microsoft Outlook, Word, Excel, PowerPoint</li></ul><ul><li>Organizational Skills – Ability to work in a fast-paced environment</li></ul><ul><li>Professionalism – Demonstrate professional standards of conduct</li></ul><ul><li>Accountability – Take pride in the work that is accomplished and understand the function/ process flow for the larger picture.</li></ul><ul><li>Communication – Express and transmit information with consistency and clarity.</li></ul><ul><li>Attention to Detail – Attend to details and pursue quality in the accomplishment of tasks</li></ul><ul><li>Adaptability – Able to respond to changing conditions, priorities, technology, and requirements.</li></ul><ul><li>Teamwork – Works cooperatively and effectively with others to reach a common goal.</li></ul><ul><li>Available to work variously weekday and/or weekend shifts, which may fluctuate. Your shift schedule may be subject to change based on business needs and customer demand</li></ul><p><b>Physical Demands</b><br />While performing the responsibilities of the job, the employee is required to be able to lift up to and including 50lbs, sit and/or stand for extended periods of time and reach with arms/hands. Walking, standing, bending, stooping, reaching, twisting, lifting, pushing, pulling, and moving items is occasionally required.</p><p><b>Work Environment</b><br />While performing the duties of this job, the employee is exposed to packaged cannabis products/supplies. The working environment can be noisy at times and temperate, the employee must have knowledge of how to manage their own personal safety under these conditions.</p><p>CannTrust is an equal opportunity employer. We thank you for your interest in employment opportunities at CannTrust. Please note, only the candidates who are selected for an interview will be contacted. CannTrust welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.</p><p>Job Type: Full-time</p><p>Work Location: Multiple Locations</p></div>","company":{"companyType":"Public/Established","name":"CannTrust","logoUrl":"/logos/canntrust-d201bb4ca139eb0b36f0ce0af7b71eca.png"},"location":{"country":"Canada","address":"Fenwick, ON","city":"Fenwick","stateProvince":"ON"},"frontendLink":"/job-posting/canntrust/technician-quality-assurance/776265b43a8c7e3af9aed9ef2587bc03","title":"Technician, Quality Assurance","category":"Medical & Healthcare","hash":"776265b43a8c7e3af9aed9ef2587bc03","postingUrl":"https://ca.indeed.com/job/technician-quality-assurance-593c47bd5c311268"},{"function":["Engineering"],"postedOn":"2 days ago","description":"<div><div><p><b>Where You Will Work:</b></p><p>Sigma Science is a New Mexico-based, 8(a) certified small business that provides comprehensive engineering and technology services to federal and commercial clients. We solve our client’s most demanding challenges by hiring best-in-class leaders and employees, and partnering with trusted companies, industry leaders, and universities. Since 1996, we have delivered technical expertise and innovative solutions to complex problems across the national security enterprise, with a focus on the nuclear industry. The key to our success is our people. Join our dynamic team as we provide industry recognized experts in a wide variety of technical fields including nuclear surety &amp; safety, information technology &amp; cybersecurity, mission assurance, nuclear security &amp; non-proliferation, and environmental management.</p><p>This position is part-time can be performed remotely with occasional travel to the site for design review meetings.</p><p><b>WHAT YOU WILL DO:</b></p><p>The Senior Engineer will provide in depth, engineering design review for the facility to include the facility systems listed below and provide review comments to address any design issue.</p><ul><li>Lightening Protection System (LPS)</li><li>Nuclear Weapons Side Flash Protection Requirements</li><li>Facility Power Systems</li><li>Fire Protection Systems</li><li>Hoist, Cranes, Winches and Similar Devices</li><li>Security Systems Security</li><li>Facility Security System Automation and Software Design Security &amp; Computer Programming</li><li>Blast Containment/Isolation Features Structural Engineering with Explosives Expertise</li><li>Electromagnetic Environment (EME) Electrical and Communication</li><li>Radiation Monitoring Nuclear Engineering HVAC Mechanical</li><li>High-Altitude Electromagnetic Pulse (HEMP)</li><li>Cyber Security</li><li>Computer Programming</li></ul><p>Ensure federal, state, and local codes concerning health, safety, and the environment are strictly adhered to in the design development cycle.</p><p>Ensure emerging technologies are incorporated in the systems design to make sure new essential systems do not become prematurely obsolete.</p><p>Respond to design Request for Information (RFI) and provide official response in a timely manner.</p><p>Perform finite element analysis (FEA) utilizing modeling and simulation software to verify design calculations.</p><p>Develop comprehensive and complete nuclear certification documents and reports including</p><ul><li>Nuclear Surety Evaluation (NSE)</li><li>Design Nuclear Safety Analysis Report (DNSAR)</li><li>Nuclear Safety Analysis Report (NSAR)</li><li>Fire Hazard Analysis (FHA)</li></ul><p><b>WHAT YOU NEED (</b>Minimum Job Requirements):</p><ul><li>Professional engineering license (PE) and a minimum of (10) years of experience in the engineering discipline</li><li>Ability to perform and stamp a 100% engineering design adequately and independently</li><li>Oversees the design, development, implementation, and analysis of technical products and systems</li><li>Broad knowledge of engineering procedures and assists in the resolution of complex problems</li><li>Expertise in one of the following fields (Mechanical, Electrical, Civil, Fire Protection, Cyber/Computer Systems, Security, Structural) with Explosives Expertise and Nuclear engineering</li><li>Ability to review in depth the facility essential systems in the duties described above</li><li>Must be U.S. Citizens with a minimum of an active DoD SECRET or DOE L security clearance</li></ul><p><b>Preferred Qualifications:</b></p><ul><li>Experience in reviewing in detail the design of the facility nuclear essential systems to verify engineering analysis &amp; calculations and compliance with regulations</li><li>Professional engineering license (PE) and (15) years of experience in the engineering discipline</li><li>Bachelor’s degree in Mechanical, Electrical, and Structural Engineering.</li></ul><p><b>EEO/AAP Statement:</b></p><p>Sigma Science is an equal opportunity/equal access/affirmative action employer that strives to develop and maintain a diverse workforce. Whatever your intersection of identities, you are welcome at Sigma. We are committed to inclusivity and promoting an equitable environment that values and respects the uniqueness of all members of our organization.</p></div></div>","company":{"name":"Sigma Science"},"location":{"country":"United States","address":"Louisiana","stateProvince":"LA"},"frontendLink":"/job-posting/sigma-science/senior-engineer-21-035/d85a550226af608b81f33fbbfb7d38e4","title":"Senior Engineer (21-035)","category":"Information Technology & Services","hash":"d85a550226af608b81f33fbbfb7d38e4","postingUrl":"https://www.indeed.com/job/senior-engineer-21-035-c6c94ca16c6c9e05"}]