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Quality Assurance/Quality Control Level 2

Sunder Desert LLC Las Vegas, NV 89122
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Who We Are

We are a California-based active lifestyle company made up of seekers, explorers, and adventurers.


Our Mission

To help people achieve a life of harmony and wellness with consciously made, science-based Cannabis products.


Our 3 Pillars of Quality

Quality of Products

Quality of Life

Quality of Community

Job Summary

We are looking for someone highly motivated, hard-working, and detail oriented to implement all QA/QC procedures to ensure the highest possible quality products. The main responsibility of this position is to constantly evaluate products at each stage of the production process; it is critical to identify, study, and help resolve any deviations from our set quality standards. Level 2 QA/QC will also collect, organize, and share data to inform the resolution of specific issues. They will also be tasked with auditing and constantly improving upon the existing systems of production.


Supervisory Responsibilities

None

Duties/Responsibilities

  • Monitor all QA/QC aspects of production, processing and packaging, and ensure that all QA/QC Processes and procedures are being followed according to our SOPs
  • Perform a daily checklist to ensure candy is standardized through to completion
  • Monitor the climate (temp and humidity) of the cure room, walk in fridge, and processing floor
  • Help production determine next steps with any standards issues they might be seeing, help identify the root cause of deviations from our quality standards. Work across departments to implement solutions that prevent continued issues.
  • Monitor and investigate valid customer complaints
  • Consistently collect data on current systems of operation
  • Help train new QA/QC hires
  • Tracking QA|QC violations
  • Work with production team and HQ to update SOPs as needed
  • Maintain site specific SOP database
  • Manage and update the QA/QC dashboard
  • Help implement new processes and track effectiveness
  • Operate all lab equipment properly without supervision
  • Assist production whenever and wherever necessary

Requirements

  • Must be age 21 or over - NV residency with valid ID is required
  • 1+ year of QA/QC Experience
  • Professional experience in food manufacturing
  • Passion for problem-solving
  • Hands-on team player with excellent communication skills
  • Detail-oriented and organized
  • Ability to manage multiple priorities/projects
  • Comfortable performing in a fast-paced working environment
  • Some experience with qualitative and quantitative analysis
  • Moderate Excel Skills
  • Familiarity with Microsoft Office Suite
  • Ability to stand for 8 hours, must be able to lift up to 50lbs.

Preferred Requirements/Qualifications


  • Six Sigma Certification(s)
  • Experience with creating, improving, and implementing SOPs
  • Experience with Agile Methodology
  • Leadership Qualities
  • Food Handlers Certification
  • Familiar with FDA, USDA, and EPA regulations

Education and Experience

  • 1+ year of QA/QC Experience
  • College degree in related field preferred

Computer Operations Abilities

  • Proficient with Microsoft Office
  • Strong data-analysis skills

Physical Requirements

  • Remaining in a stationary position, often standing or sitting for prolonged periods. Sedentary work that primarily involves sitting/standing.
  • Moving about to accomplish tasks or moving from one work site to another.
  • Repeating motions that may include the wrists, hands, and/or fingers.
  • Light work that includes moving objects up to 50 pounds.

EEO Statement

Sunderstorm is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex, gender, gender identity, pregnancy, childbirth or related medical condition, religious creed, physical disability, mental disability, age, medical condition (cancer), marital status, veteran status, sexual orientation, genetic information, or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities, and general treatment during employment.

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They will also be tasked with auditing and constantly improving upon the existing systems of production.</p><br /><p></p><h2><b>Supervisory Responsibilities</b></h2><p>None</p><h2><b>Duties/Responsibilities</b></h2><ul><li>Monitor all QA/QC aspects of production, processing and packaging, and ensure that all QA/QC Processes and procedures are being followed according to our SOPs</li><li>Perform a daily checklist to ensure candy is standardized through to completion</li><li>Monitor the climate (temp and humidity) of the cure room, walk in fridge, and processing floor</li><li>Help production determine next steps with any standards issues they might be seeing, help identify the root cause of deviations from our quality standards. Work across departments to implement solutions that prevent continued issues.</li><li>Monitor and investigate valid customer complaints</li><li>Consistently collect data on current systems of operation</li><li>Help train new QA/QC hires</li><li>Tracking QA|QC violations</li><li>Work with production team and HQ to update SOPs as needed</li><li>Maintain site specific SOP database</li><li>Manage and update the QA/QC dashboard</li><li>Help implement new processes and track effectiveness</li><li>Operate all lab equipment properly without supervision</li><li>Assist production whenever and wherever necessary</li></ul><br /><p></p><h2><b>Requirements</b></h2><ul><li>Must be age 21 or over - NV residency with valid ID is required</li><li>1+ year of QA/QC Experience</li><li>Professional experience in food manufacturing</li><li>Passion for problem-solving</li><li>Hands-on team player with excellent communication skills</li><li>Detail-oriented and organized</li><li>Ability to manage multiple priorities/projects</li><li>Comfortable performing in a fast-paced working environment</li><li>Some experience with qualitative and quantitative analysis</li><li>Moderate Excel Skills</li><li>Familiarity with Microsoft Office Suite</li><li>Ability to stand for 8 hours, must be able to lift up to 50lbs.</li></ul><br /><p></p><p><b>Preferred Requirements/Qualifications</b></p><br /><p></p><ul><li>Six Sigma Certification(s)</li><li>Experience with creating, improving, and implementing SOPs</li><li>Experience with Agile Methodology</li><li>Leadership Qualities</li><li>Food Handlers Certification</li><li>Familiar with FDA, USDA, and EPA regulations</li></ul><br /><p></p><h2><b>Education and Experience</b></h2><ul><li>1+ year of QA/QC Experience</li><li>College degree in related field preferred</li></ul><h2><b>Computer Operations Abilities</b></h2><ul><li>Proficient with Microsoft Office</li><li>Strong data-analysis skills</li></ul><br /><p></p><p><b>Physical Requirements</b></p><ul><li>Remaining in a stationary position, often standing or sitting for prolonged periods. Sedentary work that primarily involves sitting/standing.</li><li>Moving about to accomplish tasks or moving from one work site to another.</li><li>Repeating motions that may include the wrists, hands, and/or fingers.</li><li>Light work that includes moving objects up to 50 pounds.</li></ul><br /><p></p><p><b>EEO Statement</b></p><p>Sunderstorm is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex, gender, gender identity, pregnancy, childbirth or related medical condition, religious creed, physical disability, mental disability, age, medical condition (cancer), marital status, veteran status, sexual orientation, genetic information, or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities, and general treatment during employment.</p></div></div>","company":{"name":"Sunder Desert LLC"},"location":{"country":"United States","address":"Las Vegas, NV 89122","city":"Las Vegas","stateProvince":"NV"},"frontendLink":"/job-posting/sunder-desert-llc/quality-assurance-quality-control-level-2/08fa2c5f3f3f9138b2025ce967a56d1e","title":"Quality Assurance/Quality Control Level 2","hash":"08fa2c5f3f3f9138b2025ce967a56d1e","postingUrl":"https://www.indeed.com/job/quality-assurancequality-control-level-2-7c90a16b1d848a05"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>Reporting to the Senior Manager, Quality Assurance Person (QAP), the Alternate Quality Assurance Person (A/QAP) is responsible for supporting the QAP and functioning as the Alternate QAP in the absence of the QAP. The A/QAP is primarily responsible for ensuring compliance with the Cannabis Act and Regulations and Good Production Practices (GPP).</p><p><b>Job Duties &amp; Responsibilities:</b></p><p>• Primarily responsible for overseeing production quality management systems, including ongoing monitoring and implementation.</p><p>• Ensure cannabis products are produced, packaged, labeled, stored, sampled, and tested in accordance with Cannabis Regulations, GPP, and SOPs.</p><p>• Assist in the release and approval of cannabis intended for sale.</p><p>• Manage employee training and assist in the development of employee training materials. Provide ongoing guidance and training to staff on SOPs and regulatory compliance.</p><p>• Assist in creating and maintaining Preventive Control Plans (PCPs) for production.</p><p>• Oversee compliance with sanitation, equipment, and pest control programs.</p><p>• Development, revision, and implementation of SOPs and batch records.</p><p>• Responsible for third-party lab testing of cannabis products, raw materials, and environmental samples, as well as retention samples onsite.</p><p>• Assist in the review of final product testing and development of final product specifications.</p><p>• Assist in vendor approval and raw material specification programs.</p><p>• Assist in deviation/incident and Corrective and Preventative Action investigations and change control programs.</p><p>• Participate in Health Canada inspections.</p><p>• Maintain current knowledge of the Cannabis Act and Regulations.</p><p><b>Requirements:</b></p><p>• MUST have a valid Health Canada Security Clearance.</p><p>• Bachelor of Science and/or technical diploma in biology, food science, or equivalent quality field.</p><p>• 2+ years of Quality Assurance experience within a regulated environment (food, cannabis, pharmaceutical). Experience in a food production environment is preferred.</p><p>• Experience with sales to provincial boards (OCS, BCLDB, AGLC) is an asset.</p><p>• Willingness to work various shifts, weekend and shift work may be required.</p><p>• Passionate and enthusiastic about Cannabis</p></div>","company":{"name":"Canna Kraft"},"location":{"country":"Canada","address":"Woodstock, ON","city":"Woodstock","stateProvince":"ON"},"frontendLink":"/job-posting/canna-kraft/quality-assurance/267ff1399dd1221c1c0ae3adba0b0760","title":"Quality Assurance","hash":"267ff1399dd1221c1c0ae3adba0b0760","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-at-canna-kraft-2655560115"},{"employmentType":"Permanent","postedOn":"9 hours ago","description":"<div><p>Gnomestar Craft Cannabis is the highly standard Health Canada licensed Cannabis producer under the Cannabis Act located in Delta British Columbia. We are currently seeking a passionate, positive, and self-motivated Quality Assurance (QA) Specialist to join our Quality Assurance team to fulfill the role of the second Alternate Quality Assurance Person (AQAP) under Health Canada’s Cannabis Regulations. This is a part/full time position offered Monday to Friday from 10:00 am - 4 pm depending on experience. This position may require shift flexibility. The QA Specialist will report to the Quality Assurance (QA) Manager and will be an essential member of a high-performing team. The ideal candidate will have experience in Hazard Analysis and Critical Control Points (HACCP) and Preventive Control Plans (PCP), Standard Operating Procedure (SOP) development, Good Documentation Practices (GDP), Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP) and Good Production Practices (GPP)/Good Agricultural Collection Practices (GACP) and have a passion for continuous improvement.</p><p><b>Primary Responsibilities: </b></p><p>· Assist in any necessary developments and improvements to manufacturing quality systems required because of any non-compliances, process quality issues, SOP and GPP.</p><p>· Develop, maintain, and implement preventive control plans, SOPs, sanitation SOPs and related forms to ensure compliance with the Cannabis Act and Regulations.</p><p>· Complete internal audits of SOP’s.</p><p>· Develop, implement, and maintain training programs to support the implementation of SOPs and GPPs.</p><p>· Review and approve all production lot records before cannabis is released and made available for sale by the Quality Assurance Person or AQAP.</p><p>· Review certificates of analysis (COA) and internal laboratory test results for compliance to specifications.</p><p>· Complete customer complaint investigations, deviation/incident investigations, root cause analysis, and corrective action/preventive action (CAPA).</p><p>· Complete finished product label and artwork verification for compliance to regulations.</p><p>· Complete vendor qualification and evaluations.</p><p>· Participate in Health Canada and customer audits and inspections, prepare responses to observations and complete all necessary corrective actions and preventive actions.</p><p>· Participate in mock recall/recall simulation exercises.</p><p>· Assist with the development and validation of analytical testing methods, sanitation validations, process, packaging validations, and shelf-life studies as required.</p><p>· Other duties as assigned.</p><p><b>Qualifications: </b></p><p>· Bachelor of Science in Microbiology, Plant Science, Plant Biotechnology, Agronomy, Chemistry, Biochemistry, Natural Sciences, Agriculture, or a related field is required.</p><p>· 2+ years of experience in Quality Assurance in cannabis, agriculture, food manufacturing, or pharmaceutical industries is an asset.</p><p>· High proficiency in English in both written and oral.</p><p>· Experience with regulatory agencies such as Health Canada or Canadian Food Inspection Agency is an asset.</p><p>· Hazard Analysis and Critical Control Point (HACCP) certification or training is considered an asset.</p><p>· Internal auditor certification or training is considered an asset.</p><p>· College Diploma or certificate in Pharmaceutical Regulatory Affairs and Quality Operations, Quality Assurance, or related field is considered an asset.</p><p>· Understanding of microbiological and analytical chemistry techniques is considered an asset.</p><p>· Experience with information technology quality assurance systems and electronic quality management systems is considered an asset.</p><p>· Experience applying statistical methods in process validations, equipment qualifications and in quality assurance is considered an asset.</p><p>· Experience designing validation study features such as sampling and testing is considered an asset.</p><p><b>Skills: </b></p><p>· Exceptional attention to detail and skilled in precision and detailed work.</p><p>· Exceptional oral and written communication skills.</p><p>· Exceptional organizational, time management, and multi-tasking skills.</p><p>· Strong problem-solving and analytical thinking skills.</p><p>· Strong work ethic and positive team attitude.</p><p>· Proven ability to effectively use Microsoft Office Applications.</p><p><b>Abilities: </b></p><p>· Capable of working efficiently independently under minimal supervision and succeed in team environments.</p><p>· Ability to follow strict SOPs.</p><p>· Ability to conduct independent research on cannabis, industry best practices, and relevant standards and regulations.</p><p>· Ability to prioritize and meet deadlines in a fast-paced environment.</p><p>· Capable of lifting 30 lbs. and ability to work in warm, humid greenhouse-like conditions.</p><p>· Capable of working in adverse conditions including high intensity lighting for short periods of time and working in an environment with continuous low-level background noise.</p><p>· Ability to work in an indoor environment with high levels of cannabis plant material that may include allergic-reaction inducing substances such as pollen.</p><p>· Ability to wear required personal protective equipment.</p><p><b>Other Qualifications: </b></p><p>· Must be able to pass a full background and criminal check.</p><p>· Must be able to obtain Health Canada approval for Alternate Quality Assurance Person (AQAP) designation and obtain Health Canada security clearance within one year of hire.</p><p>· Previous experience working with cannabis under Health Canada regulations (MMAR/ACMPR/Cannabis Regulations) is considered an asset.</p><p>· Knowledge of the Cannabis Act and Regulations and Food and Drugs Act and Regulations is considered an asset.</p><p>If you are looking for a dynamic growth environment, with the opportunity to learn and grow in a burgeoning industry – apply with us today!</p><p>Gnomestar values the diversity of the individuals we hire and serve. All applicants, including those who require disability accommodation, will receive consideration for employment regardless of race, religion, colour, gender, gender identity or expression, sex, national origin, disability, age, or veteran status. Gnomestar actively works to identify and eliminate discriminatory barriers in the workplace.</p><p>Please apply through Indeed with your resume and cover letter for consideration. We thank all who apply but we will only contact those candidates that will be considered for an interview.</p><p>Job Types: Permanent</p><p>Salary: $22.00-$29.00 per hour</p><p>Schedule:</p><ul><li>4-6 hour shifts</li><li>flexibility</li><li>Day shift</li><li>Monday to Friday</li></ul><p>Application question(s):</p><ul><li>What is your Bachelor's Degree in?</li></ul><p>Education:</p><ul><li>Bachelor's Degree (required)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 2 years (preferred)</li><li>Health Canada or Canadian Food Inspection: 1 year (preferred)</li><li>Microsoft Office: 1 year (preferred)</li></ul><p>Licence/Certification:</p><ul><li>HACCP Certification (preferred)</li><li>Quality Assurance Certificate or similar (preferred)</li></ul><p>Reference ID: 005</p><p>Part-time hours: 30 per week</p><p>Job Type: Part-time</p><p>Salary: $22.00-$28.00 per hour</p><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Startup","name":"Gnomestar Craft Cannabis","logoUrl":"/logos/craft-cannabis-company-a1cab9d377f9c9417a2fb55622c158d2.png"},"location":{"country":"Canada","address":"Delta, BC","city":"Delta","stateProvince":"BC"},"frontendLink":"/job-posting/gnomestar-craft-cannabis/quality-assurance-technician/99174998a341e4f8932322a1a90a787b","title":"Quality Assurance Technician","hash":"99174998a341e4f8932322a1a90a787b","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-636c544d74737e16"},{"employmentType":"Full-time, Permanent","postedOn":"6 days ago","description":"<div><p><b>Position Summary: </b></p><p>Reporting to the Director of Quality Assurance &amp; Compliance the Quality Control Technician is accountable for assisting in the implementation and ongoing monitoring of the quality assurance and control systems in all activities relating to the cultivation and processing of cannabis and cannabis products in strict compliance with Health Canada regulations.</p><p><b>Responsibilities: </b></p><p>· Under the direction of the QA Manager, implement and ensure efficiency of the Quality Assurance System for all tasks relating to processing of cannabis</p><p>· Under the direction of the QA Manager, implement new SOPs as required and verify compliance with outlined procedures in current SOPs</p><p>· Assist as needed with preventative maintenance program, approved supplier program, training program</p><p>· Collect samples from incoming raw materials, release for use in production</p><p>· Collect samples from production lines for finished goods, in process materials</p><p>· Verify printed labels for compliance</p><p>· Perform spot-inspections on production line for in-process quality checks</p><p>· Maintain environmental monitoring program</p><p>· Assist with CoA compilation as required</p><p>· Verify electronic inventory records, perform on floor review of records including sanitation and logbook</p><p>· Perform batch record review, when necessary</p><p>· Confirm inventory checks and issue materials for processing</p><p>· Verify production equipment records for preventative maintenance purposes and calibrations</p><p>· Work closely with purchasing and production staff to assess incoming production materials for suitability in the facility</p><p>· Assist QA in management of CAPA and deviation program and conduct investigations into effectiveness of corrective and preventative actions</p><p>· Other duties as may be assigned from time to time</p><p><b>Qualifications: </b></p><p>· B.Sc. degree in an applicable discipline of science (Chemistry, Biochemistry, Biology or related field); or equivalent work experience</p><p>· Minimum 1 years’ experience working in quality assurance</p><p>· Knowledge of the Cannabis Act, Access to Cannabis for Medical Purposes Regulations, Food and Drugs Act, Controlled Drug and Substance Act, Pest Control Products Act, and Safe Food for Canadians Regulations or familiarity with reading and interpreting acts and regulations beneficial</p><p>· Ability to understand SOP requirements and experience training other staff in acting in compliance with relevant SOPs</p><p>· Flexible availability as evening and weekend shifts required</p><p>· Strong attention to detail, organizational skills, computer skills, verbal and written communication skills, and meticulous record keeping</p><p>· Our ideal candidate is a team player who thrives in a fast-paced environment with a proven ability to manage multiple priorities while maintaining an excellent standard of attention to detail</p><p>· Must be able to pass security clearance per Health Canada Regulations.</p><p>Application deadline: 2021-08-16</p><p>Expected start date: 2021-08-23</p><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Dental care</li><li>Disability insurance</li><li>Extended health care</li><li>Life insurance</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>COVID-19 considerations:<br />COVID-19 precautions in place.</p><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Tidal Health Solutions Ltd.","logoUrl":"/logos/tidal-health-solutions-ltd-54b2c39bf898a132bb122e791a36a861.jpeg"},"location":{"country":"Canada","address":"Saint Stephen, NB","city":"Saint Stephen","stateProvince":"NB"},"frontendLink":"/job-posting/tidal-health-solutions-ltd/quality-control-technician/0801ff7f30b676bca8f84e81aa1c09b4","title":"Quality Control Technician","hash":"0801ff7f30b676bca8f84e81aa1c09b4","postingUrl":"https://ca.indeed.com/job/quality-control-technician-c52754ea1028d70e"},{"employmentType":"Full-time, Permanent","postedOn":"2 days ago","description":"<div><p>Our client is a medical cannabis producer who operates a state-of-the-art facility just outside of the Edmonton, Alberta region.</p><p>We’re searching for a <b>Quality Assurance Technician</b> who will be responsible for ensuring product specifications are met and enforcing company standard operating procedure and policies (SOPs) on the production floor. You will be tasked with improving and maintaining test data, completing measurements, and communicating results.</p><p><b>You will be: </b></p><ul><li>Performing daily monitoring of production/GMP areas, including sanitation checks, packaging monitoring, pest control, plant counts, etc.</li></ul><ul><li>A champion of the QA department and of Good Production Practices</li></ul><ul><li>Communicating compliance deviations to leads to determine best course of action, NCR requirements, etc. while maintaining good relationships with each department</li></ul><ul><li>Assisting in development of SOPs and technical writing as directed</li></ul><ul><li>Participating in internal and external audits</li></ul><ul><li>Contributing to the continuous improvement initiatives and QA initiatives as directed</li></ul><p><b>We’re looking for: </b></p><ul><li>1 - 2 years within a cannabis, pharmaceutical, or food manufacturing industry</li></ul><ul><li>Post-secondary education in science, food manufacturing, or related.</li></ul><ul><li>Familiarity of computer usage and comfortable using Microsoft Office suite of programs</li></ul><ul><li>Ability to lift up to 50lbs</li></ul><ul><li>Class 5 license and reliable transportation</li></ul><ul><li>Security Clearance from Health Canada is an asset</li></ul><ul><li>Food safety/sanitation focused tickets- CFPM, FSP, HAACP, etc</li></ul><ul><li>Working knowledge of C15, Sage, or other ERP systems</li></ul><ul><li>A positive attitude; someone who likes to build relationships with other departments</li></ul><ul><li>Awareness of the Cannabis Act</li></ul><ul><li>Diligent time management skills</li></ul><p><i>We appreciate the interest from all candidates; however, we will be contacting only those that best fit our client’s requirements.</i></p><p><i>Terra Recruitment welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.</i></p><p>Job Types: Full-time, Permanent</p><p>Salary: $45,000.00-$50,000.00 per year</p><p>Benefits:</p><ul><li>Dental care</li><li>Extended health care</li></ul><p>Schedule:</p><ul><li>10 hour shift</li><li>8 hour shift</li></ul><p>Ability to commute/relocate:</p><ul><li>Edmonton, AB: reliably commute or plan to relocate before starting work (preferred)</li></ul><p>Experience:</p><ul><li>cannabis industry: 2 years (preferred)</li><li>QA experience in GPP/GMP Facilities: 2 years (preferred)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"name":"Terra Recruitment Inc."},"location":{"country":"Canada","address":"Edmonton, AB","city":"Edmonton","stateProvince":"AB"},"frontendLink":"/job-posting/terra-recruitment-inc/quality-assurance-technician/3488654fa818ea84a5d372a889a58e9c","title":"Quality Assurance Technician","hash":"3488654fa818ea84a5d372a889a58e9c","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-479db359c3200eb0"},{"employmentType":"Full-time","postedOn":"18 days ago","description":"<div><p><b>We are looking for a highly motivated Quality Assurance and Production Assistants. This is a great opportunity to earn some experience in the Quality Assurance field. The QAA's will be working on SOP's, Batch Records, inventory control, as well as other jobs related to the production and packaging of products. The Cannabis industry is a highly regulated space by Health Canada. This position will be focused on cannabis edibles - We are working with a world-renowned Chocolatier.Part-time hours: 20-40 per weekExpected start date: 2021-07-05Job Types: Full-time, Part-time, PermanentSalary: $30,000.00-$40,000.00 per yearBenefits:</b></p><p>• Extended health care</p><p>• Paid time off</p><p><b>Schedule:</b></p><p>• 8 hour shift</p><p><b>Education:</b></p><p>• Bachelor's Degree (preferred)</p><p><b>Experience:</b></p><p>• Quality Assurance: 1 year (preferred)</p><p><b>Work remotely:</b></p><p>• No</p></div>","company":{"name":"Palm Gardens Cannabis Company"},"location":{"country":"Canada","address":"Edmonton, AB","city":"Edmonton","stateProvince":"AB"},"frontendLink":"/job-posting/palm-gardens-cannabis-company/quality-assurance/96ff1ec13f01403ca6e5b295271c3c90","title":"Quality Assurance","hash":"96ff1ec13f01403ca6e5b295271c3c90","postingUrl":"https://ca.mncjobz.com/jobs/quality-assurance-edmonton-1110300"},{"employmentType":"Full-time, Permanent","postedOn":"6 days ago","description":"<div><p><b>Position Summary: </b></p><p>Reporting to the Director of Quality Assurance &amp; Compliance the Quality Assurance Technician is accountable for assisting in the development, implementation, and ongoing monitoring of the quality assurance systems in all activities relating to the cultivation, and processing of cannabis and cannabis products in strict compliance with Health Canada regulations. They are also responsible for assisting the Director with compliance activities.</p><p><b>Responsibilities: </b></p><p>· Develop, implement, and ensure efficiency of the Quality Management System for all tasks relating to cultivation and processing of cannabis;</p><p>· Prepare and implement new SOPs as required and verify compliance with outlined procedures</p><p>· Collaborate with Quality Teams, Regulatory Compliance, and Production to ensure compliance with the Health Canada regulations in all activities;</p><p>· Assist with management of preventative maintenance program, approved supplier program, training program and participate in internal audits;</p><p>· Conduct batch record review and release under the supervision of Director;</p><p>· Audit production equipment records for preventative maintenance purposes and calibrations.</p><p>· Manage material files, room files, and equipment files and work closely with purchasing and production staff to assess incoming production materials for suitability in the facility;</p><p>· Assist with monthly reporting duties as required to Health Canada and CRA;</p><p>· Assist in management of CAPA and deviation program and conduct investigations into effectiveness of corrective and preventative actions;</p><p>· Conduct quality review risk assessment of new processes and assist in preparation of process control plan as required;</p><p>· Assist in recall program, including biannual mock recall tests;</p><p>· Continuous self-guided education in industry standards and best practices to continually improve processes and efficiency</p><p>· Participate in 3rd party audits with suppliers and regulatory bodies</p><p><b>Qualifications: </b></p><p>· B.Sc. degree in an applicable discipline of science (Chemistry, Biochemistry, Biology or related field);</p><p>· 1-3 years’ experience working in quality assurance;</p><p>· Knowledge of the Cannabis Act, Access to Cannabis for Medical Purposes Regulations, Food and Drugs Act, Controlled Drug and Substance Act, Pest Control Products Act and Safe Food for Canadians Regulations; or familiarity with reading and interpreting acts and regulations;</p><p>· Ability to understand SOP requirements and mentor other staff in acting in compliance with relevant SOPs;</p><p>· Flexible availability; weekend shifts may be required;</p><p>· Advanced knowledge of GMP and regulations for manufacturing pharmaceutical and/or food products will be considered an asset;</p><p>· Strong attention to detail, organizational skills, computer skills, verbal and written communication skills, and meticulous recordkeeping;</p><p>· Our ideal candidate is a team player who thrives in a fast-paced environment with a proven ability to manage multiple priorities while maintaining an excellent standard of attention to detail;</p><p>· Must be able to pass security clearance per Health Canada Regulations.</p><p>Application deadline: 2021-08-16</p><p>Expected start date: 2021-08-23</p><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Dental care</li><li>Disability insurance</li><li>Extended health care</li><li>Life insurance</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>COVID-19 considerations:<br />COVID-19 precautions taken.</p><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Tidal Health Solutions Ltd.","logoUrl":"/logos/tidal-health-solutions-ltd-54b2c39bf898a132bb122e791a36a861.jpeg"},"location":{"country":"Canada","address":"Saint Stephen, NB","city":"Saint Stephen","stateProvince":"NB"},"frontendLink":"/job-posting/tidal-health-solutions-ltd/quality-assurance-technician/b14e01ad38ea80f56c5abe6cedfa7add","title":"Quality Assurance Technician","hash":"b14e01ad38ea80f56c5abe6cedfa7add","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-521538b762f742b3"},{"employmentType":"Full-time, Permanent","postedOn":"8 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><b>ABOUT US: </b></p><p>BZAM is as awesome as it sounds! We are an integrated cannabis company whose mission and brand stand for quality and integrity. Our commitment to excellence, service and employee satisfaction is demonstrated in our agile and strategic approach to market entry and investment in our people. As an emerging company in a rapid growth industry, BZAM’s innovative and accomplished leadership team is the cornerstone of our business and portfolio development.</p><p><b>YOUR </b><b>CONTRIBUTION: </b></p><p>Ø Ensure that all production activities are carried out as per Standard Operating Procedures (SOP) and in compliance with GPP;</p><p>Ø 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;</p><p>Ø Enforce procedural and GPP requirements including health and hygiene, gowning, sanitation and documentation practices;</p><p>Ø Coordinate change control implementation perform risk and impact assessment;</p><p>Ø Review status of process materials and ensure proper control, hold, release and transfer of materials;</p><p>Ø Assist in receiving inspections, verifications of BOMS and balances;</p><p>Ø Perform environmental verifications, pre-line clearance, and in-process checks;</p><p>Ø Ensure that cannabis is destroyed as per current approved SOPs and in line with the Cannabis Regulations;</p><p>Ø Ensure appropriate sample collection and testing;</p><p>Ø Coordinate calibration, maintenance and pest control activities;</p><p>Ø Provide assistance in resolving technical problems, process deviations, quality investigations, and corrective actions;</p><p>Ø Verify logs, databases, trends, and other data to track and flag quality concerns and areas of improvement; and</p><p>Ø Other duties as assigned by Quality Assurance Manager &amp; Quality Assurance Specialist as applicable.</p><p><b>WHAT YOU BRING: </b></p><p>Ø BSc. in Chemistry, Biology, Pharmacology, Food Science, Microbiology or Environmental Science;</p><p>Ø Strong ethics coupled with respect for the highest compliance standards;</p><p>Ø Strong and current knowledge of Good Agricultural Practice, Good Manufacturing Practice, regulatory and environmental guidelines as per the Cannabis Regulations;</p><p>Ø Problem-solving and decision-making skills;</p><p>Ø Computer proficiency including MS Office; and</p><p>Ø Excellent communication skills.</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><b>YOUR EXPERIENCE: </b></p><p>Ø 2-3 years’ experience within a Quality Control position;</p><p>Ø Proven knowledge and experience in the stated responsibilities of the position (i.e. Food, Pharma, NHP);</p><p>Ø 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</p><p>Ø Preferred experience with cGMP, GAP, GLP, HACCP, ISO and FDA.</p><p><b>WHAT WE OFFER: </b></p><p>Ø Competitive Compensation and Benefits Package</p><p>Ø Rapid growth and advancement potential</p><p>Ø Learning and development opportunities</p><p>Ø Dynamic and innovative environment</p><p>Ø Exceptional culture</p><p><b><i>BZAM is an Equal Employment Opportunity employer that values the strength of diversity within the workplace. All qualified applicants, regardless of race, colour, religion, gender, sexual orientation, marital status, gender identity or expression, nationality, age, disability or veteran status, or any other characteristic protected by applicable law, are strongly encouraged to apply.</i></b></p><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Dental care</li><li>Extended health care</li><li>RRSP match</li><li>Vision care</li></ul><p>COVID-19 considerations:<br />BZAM Cannabis is committed to following all provincial and federal public health authority guidance pertaining to COVID-19</p><p>Education:</p><ul><li>Bachelor's Degree (preferred)</li></ul><p>Experience:</p><ul><li>Quality Control: 2 years (preferred)</li><li>Manufacturing: 1 year (preferred)</li><li>Cannabis: 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","hash":"8878a9465fd0ee02317b32ad37b44311","postingUrl":"https://ca.indeed.com/job/quality-control-associate-7b29e87073e7e6da"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>AM Shift: 6:00AM – 4:30PM, Monday to Thursday, Friday as needed</p><p>PM Shift: 1:00PM – 11:30PM, Monday to Thursday, Friday as needed</p><p>The Quality Assurance Technician, under the direction of the Senior Quality Assurance Manager, is primarily responsible for the monitoring and quality control of cannabis production on the production floor. The role will also be responsible for ensuring compliance with various regulations and as it pertains to the Cannabis industry as well as Good Production Practices (GPP). The incumbent will review documents to ensure the completed document is compliant with Aleafia Standard Operating Procedures ( SOP’s ) and current Good Production Practices.</p><p>ESSENTIAL FUNCTIONS</p><ul><li>Ensure that all Company standard operating procedures are being strictly followed.</li></ul><ul><li>Ensure compliance with Cannabis Regulations (CR).</li></ul><ul><li>Help implement and maintain GPP.</li></ul><ul><li>Conduct in-line verification quality checks.</li></ul><ul><li>Collaborate with other departments to ensure compliance with standard operating procedures.</li></ul><ul><li>Review batch records and supporting documentation daily (i.e. logbooks, forms)</li></ul><ul><li>Identify incomplete documents and / or corrections and meet with the individual (s) on the production floor to arrange for corrections.</li></ul><ul><li>Perform internal QA inspections that are compliant with corporate policies, practices, and procedures.</li></ul><ul><li>Adopt and incorporate quality methods into everyday work.</li></ul><ul><li>Identify relevant QA training needs and opportunities.</li></ul><ul><li>Troubleshoot with production/operations regarding on the floor quality issues</li></ul><ul><li>Verify, organize, compile and file daily production records.</li></ul><ul><li>Ensure that garbage and cannabis products are managed or destroyed in accordance with Cannabis Regulations (CR).</li></ul><ul><li>Complete inspection on production equipment, sanitation practices, and production areas.</li></ul><ul><li>Train staff on operating procedures and GPP.</li></ul><ul><li>Recommend corrective action.</li></ul><ul><li>Adhere to all occupational health and safety regulations.</li></ul><ul><li>Other duties as assigned.</li></ul><p>ROLE REQUIREMENTS/ABILITIES</p><p>Experience / Education</p><ul><li>Diploma in biological science (chemistry, biology, pharmacology) and/or 1-2 years of relevant work experience is required.</li></ul><ul><li>Experience in pharmaceutical, food, cannabis, or a related industry would be considered an asset.</li></ul><p>Skills &amp; Abilities</p><ul><li>Experience with an organization regulated by HACCP Canada or experience in a similarly regulated environment (GMP, GAP, GPP)</li></ul><ul><li>Ability to influence others to do things while maintaining integrity and trust, by keeping a continuous focus on effective communications to ensure achievement of shared goals.</li></ul><ul><li>Ability to follow strict operating procedures</li></ul><ul><li>Ability to work individually as well as part of a team</li></ul><ul><li>High attention to detail</li></ul><ul><li>Strong organizational skills to handle the high amount of documentation reviewed by this position.</li></ul><ul><li>Ability to work in a deadline-oriented environment</li></ul><ul><li>Ability to adapt to new technology</li></ul><ul><li>Dedication to safety measures and best practices</li></ul><ul><li>Ability to prioritize and manage conflicting demands</li></ul><ul><li>Ability to effectively communicate in English both verbally and in writing</li></ul><ul><li>High level of integrity and work ethic</li></ul><ul><li>Knowledge of The Cannabis Act and its supporting regulations is an asset</li></ul><ul><li>Must have own transportation as we are not on a public transportation route</li></ul><ul><li>Proficiency in Microsoft Office is required</li></ul><ul><li>Proficiency in Ample organics is considered an asset</li></ul><p>Other Requirements</p><ul><li>Available to work flexible hours as required</li></ul><ul><li>Overtime may be required to complete a task after the shift has ended.</li></ul><p>Physical Demands</p><ul><li>100% indoor climate-controlled work</li></ul><ul><li>Working while wearing PPE equipment (coveralls/Tyvek suits, respirators, safety footwear, gloves, face mask and eye protection, hair and/or beard net)</li></ul><ul><li>Lift 25lbs and up to 50lbs</li></ul><ul><li>Standing for long periods of time</li></ul><p>Working Conditions</p><ul><li>Constant exposure to the smell of cannabis</li></ul><ul><li>Repetitive work</li></ul><ul><li>Manual dexterity required to use desktop computer</li></ul><ul><li>Working in a busy environment</li></ul><ul><li>Use of required personal protective equipment</li></ul><ul><li>Overtime as required</li></ul><p>Note: The chosen applicant will be required to successfully complete reference checks and a criminal background check.</p><p>We appreciate the interest by all candidates however we will be contacting those that best fit the requirements. If you are selected to participate in the recruitment process, please inform Human Resources of any accommodations you may require. Aleafia Health will work with you in an effort to ensure that you are able to fully participate in the process.</p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Dental care</li><li>Extended health care</li><li>On-site parking</li><li>Stock options</li></ul><p>Schedule:</p><ul><li>10 hour shift</li><li>Monday to Friday</li></ul><p>Application question(s):</p><ul><li>Do you have a Diploma in biological science (chemistry, biology, pharmacology)?</li></ul><p>Experience:</p><ul><li>Quality assurance: 2 years (preferred)</li><li>pharmaceutical, food, cannabis: 1 year (preferred)</li></ul></div>","company":{"companyType":"Public/Established","name":"Aleafia Health","logoUrl":"/logos/aleafia-health-ac08d53955eeb3e31b5b8dfd5dfcf63f.jpeg"},"location":{"country":"Canada","address":"Paris, ON","city":"Paris","stateProvince":"ON"},"frontendLink":"/job-posting/aleafia-health/quality-assurance-technician/abe03c8d88c7ef9b1352d5aad4eaf964","title":"Quality Assurance Technician","hash":"abe03c8d88c7ef9b1352d5aad4eaf964","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-1941a0e2d25ea6da"},{"employmentType":"Full-time","postedOn":"13 days ago","description":"<div><p><b>QC Technician </b></p><p>The Quality Control (QC) technician at Galaxie Brands Corp is a crucial part of all manufacturing operations. The QC teach will support daily, weekly and monthly quality testing, inspections and procedures. This role is responsible for alerting any quality issues to the attention of the QAP and ensure the issues are solved efficiently. With a keen eye for detail, the QC Tech is responsible for performing routine testing to ensure quality and adherence to regulations and standards. They will conduct risk assessments and corrective action solutions. The QC Tech will support production manager with product and supplier issues.</p><p>The Quality Control Technician reports directly to the Quality Assurance lead or QAP and will be responsible for monitoring and quality control of cannabis production. The role will also be responsible for ensuring compliance with internal Standard Operating Procedures (SOP’s), Good Production Practices (GPP) and Good Manufacturing Practices (GMP).</p><p><b>Position Responsibilities</b></p><ul><li>Represent Quality Department on the production floor.</li><li>Support and guarantee product quality and safety at every step of the production process to ensure product manufactures in compliance with Act of Cannabis and cannabis regulations.</li><li>Perform in process-checks and label verification on the floor.</li><li>Verify production tasks that are completed according to good documentation practices.</li><li>Verify non-cannabis incoming materials and perform AQL inspection as needed.</li><li>Report any deviation to the lead and assist in investigation, as necessary.</li><li>Verify sanitation documentation and activity logbooks (room and equipment) prior to line clearance and start up approval.</li><li>Ensure that SOPs are followed/implemented at every step of the process from the point of receiving cannabis through manufacturing and until shipment of bulk cannabis and/or cannabis product.</li><li>Assist QC inspectors in performing swabs in production areas.</li><li>Perform other duties as directed by QA/QC Lead or QAP/A</li></ul><p><b>Competencies</b></p><ul><li>Evaluate data and draft reports, noting any relevant deviations from existing standards</li><li>Identify areas for quality control improvement and implement new methods accordingly</li><li>Communicate quality or compliance concerns with urgency</li><li>Responsible for monitoring, and programing critical control points (CCP).</li><li>Responsible for monitoring and product food safety and quality throughout the manufacturing process.</li><li>Responsible for performing sanitation verification and allergen testing on equipment and other areas required.</li><li>Responsible for the correct recording and filing of all relevant record logs and Documentation.</li><li>Ensures employees are following all GMP, Food Safety and worker safety practices.</li><li>Collect product samples for Product Development, lab retains and the laboratory when directed.</li><li>Perform inspections on Products, Equipment and Machinery.</li></ul><p><b>Minimum Requirements</b></p><ul><li>Post-secondary education in Science, Quality, or a related discipline.</li><li>Minimum 1-2 years of professional related experience in Quality Assurance/Quality Control within a cannabis, food or pharmaceutical manufacturing environment.</li><li>Knowledge of Act of cannabis and cannabis regulations, ACMPR, ISO, HACCP, SQF, GFSI, or other quality systems.</li><li>Good written and spoken communication skills.</li><li>Proficient in MS Office (Word, Excel, Outlook, PPT)</li><li>Assist Quality Operations Associates in checking all batch related documentation for QAP review and approval prior to release.</li><li>Ability to work in a fast-paced environment.</li><li>Maybe required to be able to lift up to 20lbs.</li><li>Flexibility and adaptability to take up additional duties and cross train</li><li>Ability to work variable shifts (continental, afternoons/nights)</li></ul><p>Job Type: Full-time</p><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>COVID-19 considerations:<br />No Mask, No Entry. All employees must submit a Covid-19 screening form and temperature check before entering the workplace.</p><p>Ability to commute/relocate:</p><ul><li>Puslinch, ON: reliably commute or plan to relocate before starting work (preferred)</li></ul><p>Licence/Certification:</p><ul><li>G or G2 Class Drivers License (preferred)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Galaxie Brands Corporation","logoUrl":"/logos/galaxie-brands-corporation-7f1bee02ccd91e92776bd6527ef67c95.jpeg"},"location":{"country":"Canada","address":"Puslinch, ON","city":"Puslinch","stateProvince":"ON"},"frontendLink":"/job-posting/galaxie-brands-corporation/quality-control-technician/6077a089319d6ae860a0af0843e358e8","title":"Quality Control Technician","hash":"6077a089319d6ae860a0af0843e358e8","postingUrl":"https://ca.indeed.com/job/quality-control-technician-90b6915337359e71"},{"postedOn":"10 days ago","description":"<div><div>About the Company:<div>Dosecann is a Canadian licensed dealer dedicated to developing Cannabis Solutions for the global cannabis industry. Dosecann has assembled a world-class team housed in a purpose-built, 52,000 sqft. GMP compliant facility that will be the hub for cannabis extraction, product innovation and formulation.</div>Overview:<div>The Quality Control department is seeking to fill a full time QC Chemist role, to support the In-Process, Intermediate, and Final product testing at Dosecann.</div><div>Reporting to the Lead Quality Control Chemist, the QC Chemist will be responsible for receiving samples into the laboratory, in process/intermediate/final material testing, equipment calibrations, quality documentation, and housekeeping duties within the laboratory. The QC Chemist will also be responsible for ordering QC supplies and updating testing status in the ERP system.<br /></div><div></div><div>Additional responsibilities may include verification of laboratory data, document creation/edit/review, and raw material support.</div>What can you expect to do:<ul><li>Manage incoming samples to the laboratory.</li><li>Review, edit, format documents from Quality Control.</li><li>Testing of all in-process, intermediate and final product in the Quality Control laboratory.</li><li>Use the internal ERP system to update receipt of materials, testing progress, and ordering of materials.</li></ul>What we are looking for :<ul><li>Minimum 2 years experience working in a laboratory setting.</li><li>Previously demonstrated attention to detail and ability to effectively follow Standard Operating Procedures (SOP’s).</li><li>Previous experience using an ERP or QMS is preferred.</li><li>Excellent communication skills (both writing and verbal).</li></ul>What will set you apart:<ul><li>Bachelor of Science degree (preferably with a focus in chemistry) or Bio-Technology diploma.</li><li>Experience in Quality Control environment.</li><li>Knowledge of GPP and/or GMP.</li><li>Positive attitude and willingness to learn.</li></ul>Â :<div>Dosecann is an equal opportunity employer and encourages applications from all qualified individuals. We thank all applicants for their interest, however, only those selected for an interview will be contacted.</div><div>We provide accommodation for job applicants with disabilities during the recruitment process in accordance with applicable laws. Please contact us to request accommodation.</div></div></div>","company":{"companyType":"Private/Growth","name":"Auxly Cannabis Group","logoUrl":"/logos/auxly-cannabis-group-inc-56917990efed42457bbac5214a4a8b4d.jpeg"},"location":{"country":"Canada","address":"Charlottetown, PE","city":"Charlottetown","stateProvince":"PE"},"frontendLink":"/job-posting/auxly-cannabis-group/quality-control-chemist/42da8a651375797466d6e06577eac831","title":"Quality Control Chemist","hash":"42da8a651375797466d6e06577eac831","postingUrl":"https://ca.indeed.com/job/quality-control-chemist-b94a12062d02244d"},{"postedOn":"10 days ago","description":"<div><div>About the Company:<div>Dosecann is a Canadian licensed dealer dedicated to developing Cannabis Solutions for the global cannabis industry. Dosecann has assembled a world-class team housed in a purpose-built, 52,000 sqft. GMP compliant facility that will be the hub for cannabis extraction, product innovation and formulation.</div>Overview:<div>The Quality Control department is seeking to fill a full time QC Chemist role, to support the In-Process, Intermediate, and Final product testing at Dosecann.</div><div>Reporting to the Lead Quality Control Chemist, the QC Chemist will be responsible for receiving samples into the laboratory, in process/intermediate/final material testing, equipment calibrations, quality documentation, and housekeeping duties within the laboratory. The QC Chemist will also be responsible for ordering QC supplies and updating testing status in the ERP system.<br /></div><div></div><div>Additional responsibilities may include verification of laboratory data, document creation/edit/review, and raw material support.</div>What can you expect to do:<ul><li>Manage incoming samples to the laboratory.</li><li>Review, edit, format documents from Quality Control.</li><li>Testing of all in-process, intermediate and final product in the Quality Control laboratory.</li><li>Use the internal ERP system to update receipt of materials, testing progress, and ordering of materials.</li></ul>What we are looking for:<ul><li>Minimum 2 years experience working in a laboratory setting.</li><li>Previously demonstrated attention to detail and ability to effectively follow Standard Operating Procedures (SOP’s).</li><li>Previous experience using an ERP or QMS is preferred.</li><li>Excellent communication skills (both writing and verbal).</li></ul>What will set you apart:<ul><li>Bachelor of Science degree (preferably with a focus in chemistry) or Bio-Technology diploma.</li><li>Experience in Quality Control environment.</li><li>Knowledge of GPP and/or GMP.</li><li>Positive attitude and willingness to learn.</li></ul>Â :<div>Dosecann is an equal opportunity employer and encourages applications from all qualified individuals. We thank all applicants for their interest, however, only those selected for an interview will be contacted.</div><div>We provide accommodation for job applicants with disabilities during the recruitment process in accordance with applicable laws. Please contact us to request accommodation.</div></div></div>","company":{"companyType":"Private/Established","name":"Dosecann Cannabis Solutions","logoUrl":"/logos/dosecann-cannabis-solutions-6b3f328363d5d612b11ccd2ddb52f6df.jpeg"},"location":{"country":"Canada","address":"Charlottetown, PE","city":"Charlottetown","stateProvince":"PE"},"frontendLink":"/job-posting/dosecann-cannabis-solutions/quality-control-chemist/21b7506596231ed720aee6bc817fc817","title":"Quality Control Chemist","hash":"21b7506596231ed720aee6bc817fc817","postingUrl":"https://ca.indeed.com/job/quality-control-chemist-a036ee8995407967"},{"postedOn":"7 days ago","description":"<div><div><h1><b>Quality Assurance Specialist</b></h1><div>Smiths Falls, ON, Canada Req #3692 </div><p>Thursday, 22 July 2021</p><div><p><b>The Company</b></p><p>At Canopy Growth, our mission is clear: improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We’re building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.</p><p>With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.</p><p></p><p>Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!</p></div><div><div><div><b>The Opportunity</b><br /></div></div><div></div><div><div><div>The Quality Assurance Specialist is accountable for the development, implementation and ongoing monitoring of the quality assurance and control systems in strict compliance with the Access to Cannabis for Medical Purposes Regulations (ACMPR). The QA Person is responsible for leading the sites Quality Assurance operations.<br /></div></div><div></div><div><div><b>Responsibilities</b></div></div><div><ul><li>Collaborate with Quality Control, Regulatory Affairs, Operations, and Marketing departments to ensure compliance with Health Canada regulations and guidelines</li><li>Lead review and enforcement to Canadian and EU cGMP</li><li>Support continuous quality improvement through participation in HACCP</li><li>Review and approval of input materials, equipment, premises, and standard operating procedures</li><li>Review and approval of product for sale</li><li>Review of quality complaints and their associated investigations</li><li>Participate in internal audits for other Canopy Growth production facilities</li><li>Other responsibilities as assigned</li></ul></div></div><div><div><div><b>Experience</b></div></div><div><ul><li>BSc in Pharmacology, Toxicology or related field (Biochemistry, Biology, Chemistry, etc)</li><li>Minimum three years’ experience in a GMP regulated environment</li><li>Experience in developing and leading continual improvement of a GMP Quality Management System</li><li>Knowledge of the Access to Cannabis for Medical Purposes Regulations, Food and Drugs Act, Controlled Drugs and Substances Act, Pest Control Products Act, and Fertilizer Act</li><li>Experience in an ISO:9001, ISO:13485, or ISO:17025 environment is considered an asset</li></ul></div></div><div><div><b>Other Details</b><br /></div></div><div></div><div><div>This is a full-time position based out of Smiths Falls.</div></div></div><div><p>We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don’t hear from us, don’t fret; every resume we get is kept in our database for six months for consideration in future searches for talent.</p><p>Canopy Growth welcomes and encourages applications from people with disabilities.</p><p>Accommodations are available upon request for candidates taking part in all aspects of the selection process.</p><p>One last note: the chosen applicant will be required to successfully complete background and reference checks.</p><p></p><p>Thank you so much for your interest in Canopy Growth.</p></div></div><p></p></div>","company":{"companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Smiths Falls, ON","city":"Smiths Falls","stateProvince":"ON"},"frontendLink":"/job-posting/canopy-growth-corporation/quality-assurance-specialist/3fa6f864e1bcfa4324b42d674dc79a42","title":"Quality Assurance Specialist","hash":"3fa6f864e1bcfa4324b42d674dc79a42","postingUrl":"https://ca.indeed.com/job/quality-assurance-specialist-5e7bc3d2c767bad7"},{"employmentType":"Full-time, Permanent","postedOn":"8 days ago","description":"<div><p>The Quality Assurance Associate will report to the Quality Assurance Manager (QAP) or Alternate QAP in lieu and designated management as required. The Quality Assurance Associate is responsible for supporting the Quality Assurance initiatives within the department to ensure that cannabis products produced meet the organization’s objectives for quality, safety, regulatory and customer expectations in accordance with the Cannabis Act and Regulations in accordance with Health Canada guidelines.</p><p><b>ABOUT US: </b></p><p>BZAM is as awesome as it sounds! We are an integrated cannabis company whose mission and brand stand for quality and integrity. Our commitment to excellence, service and employee satisfaction is demonstrated in our agile and strategic approach to market entry and investment in our people. As an emerging company in a rapid growth industry, BZAM’s innovative and accomplished leadership team is the cornerstone of our business and portfolio development.</p><p><b>YOUR </b><b>CONTRIBUTION: </b></p><p>Ø Support the Quality Assurance Department in implementing SOPs &amp; Quality Management Programs and projects to ensure GPP compliance under the Cannabis Act/Regulations; work cross-departmentally to implement SOPs (i.e. Operations, Regulatory, Security);</p><p>Ø Assist in implementation of training programs around SOPs pertaining to GPP and Record Keeping Compliance; collaborate training programs with Human Resources and assess training gaps continuously;</p><p>Ø Support the QA Department’s quality programs/systems for cannabis storage;</p><p>Ø Assist in the implementation of programs around GPP &amp; Record Keeping Methods for sanitation of premises, equipment, cleanliness, hygienic behaviour of personnel, and facility maintenance;</p><p>Ø Collaborate with Regulatory and Security Departments to develop and perform internal audits regularly to determine quality assurance compliance according to Cannabis Regulations;</p><p>Ø Maintain current knowledge of best practices for the provisions of the Cannabis Act and Cannabis Regulations that apply to the license holder; and</p><p>Ø Other duties as assigned.</p><p><b>WHAT YOU BRING: </b></p><p>Ø BSc. in Chemistry, Biology, Pharmacology or Food Science, obtained or recognized by a Canadian University;</p><p>Ø 3+ years’ professional experience in Quality Assurance/Control in a production environment;</p><p>Ø Preferred knowledge of plant chemistry, extraction and formulation systems, and chromatographic techniques;</p><p>Ø Recent criminal record check completed (required prior to hiring);</p><p>Ø Solid ERP, MS Office Suite, Adobe Pro, G-Suite and additional technical proficiency; and</p><p>Ø Valid security clearance (ACMPR or Cannabis Regulations).</p><p>You Are FOCUSED, DETAIL ORIENTED, AND METHODICAL. Nothing gets by you and you are a master at time management.</p><p>You are a CLEAR COMMUNICATOR capable of speaking and writing professionally, clearly and concisely.</p><p>You are a RESEARCH GURU, proficient in researching and retaining complicated compliance knowledge.</p><p>You are ORGANIZED and strongly skilled in the area of project management.</p><p><b>YOUR EXPERIENCE: </b></p><p>Ø Proven knowledge and demonstrable experience in the stated responsibilities of the position (i.e. Food, Pharma, NHP);</p><p>Ø Experience in creating and supporting process enhancement initiatives to maintain an environment of continuous learning and improvement;</p><p>Ø Preferred experience with cGMP, GAP, GLP, HACCP, ISO and FDA;</p><p>Ø Preferred experience with design inspection methods, fabrication and production of medical cannabis; and</p><p>Ø Experience working with technical reports, hazard critical control analysis, and inspecting production resources and materials.</p><p><b>WHAT WE OFFER: </b></p><p>Ø Competitive Compensation and Benefits Package</p><p>Ø Rapid growth and advancement potential</p><p>Ø Learning and development opportunities</p><p>Ø Dynamic and innovative environment</p><p>Ø Exceptional culture</p><p><b><i>BZAM is an Equal Employment Opportunity employer that values the strength of diversity within the workplace. All qualified applicants, regardless of race, colour, religion, gender, sexual orientation, marital status, gender identity or expression, nationality, age, disability or veteran status, or any other characteristic protected by applicable law, are strongly encouraged to apply.</i></b></p><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Dental care</li><li>Extended health care</li><li>RRSP match</li><li>Vision care</li></ul><p>COVID-19 considerations:<br />BZAM Cannabis is committed to following all provincial and federal public health authority guidance pertaining to COVID-19</p><p>Education:</p><ul><li>Bachelor's Degree (preferred)</li></ul><p>Experience:</p><ul><li>Quality assurance: 3 years (preferred)</li><li>Manufacturing: 1 year (preferred)</li><li>Cannabis: 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-assurance-associate/06f2c6939aede892381936d3bd87e59a","title":"Quality Assurance Associate","hash":"06f2c6939aede892381936d3bd87e59a","postingUrl":"https://ca.indeed.com/job/quality-assurance-associate-12c46664e9771edd"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p><b>QUALITY ASSURANCE ASSOCIATE</b></p><p><b>Location: </b>Markham, ON</p><p><b>MAIN RESPONSIBILITIES: </b></p><ul><li>Ensure completeness of documentation by reviewing all documentation is GMP/GDP compliant</li><li>Submit samples for analytical testing as outlined in SOPs.</li><li>Obtain representative samples from shipments of received materials (RM, PM, FPB, FP) in accordance with company Standard Operating Procedures (SOPs) and ensure all appropriate documentation is maintained.</li><li>Maintain retained samples in a designated room and maintain accurate retained sample inventories.</li><li>Assist with complaint investigation and root cause analysis</li><li>Prepare monthly reports</li><li>Review and maintain completed batch records.</li><li>Maintain all QC records, in accordance with Aurora’s SOPs.</li><li>Perform in-process QC checks during production events.</li><li>Participate in internal ISO, GMP and safety audits.</li><li>Assist in conducting internal quality audits.</li><li>Participate in regulatory audits (Health Canada, other regulatory bodies, etc.)</li><li>Ensure the timely completion of all preventive and corrective actions necessary to resolve any non-conformance issues that may have been highlighted as a result of the audits.</li><li>Ensure product is moving through product lifecycle in the facility in a linear manner, as per Aurora’s SOPs.</li><li>Maintain security and confidentiality of all aspects of the business</li><li>Where applicable, must adhere to Aurora's SOPs and comply with Health Canada’s Cannabis Act. In addition, must adhere to all ISO requirements and the Occupational Health and Safety Act (OHSA)</li><li>Where applicable, promote and maintain GMP requirements.</li><li>Maintain GMP, ISO 9001, ISO 14001, OHSAS 18001 management systems.</li><li>Assist in training staff for ISO 9001, ISO 14001, OHSAS 18001 management systems.</li><li>Other duties as required.</li></ul><p><b>QUALIFICATIONS: </b></p><ul><li>Bachelor’s Degree or diploma in a related scientific field.</li><li>A minimum of two to five years of quality assurance experience preferred.</li><li>Demonstrated ability to work with others as a member of a team.</li><li>Knowledge of health and safety standards and compliance.</li><li>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.</li><li>Demonstrated ability to understand and execute verbal and written instructions.</li><li>Proficiency to prioritize activities.</li><li>Demonstrated problem solving skills and attention to detail.</li><li>Capability to maintain both physical and mental fitness and alertness.</li><li>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.</li></ul><p>We would like to thank all applicants for their interest but only those selected for an interview will be contacted.</p><p><b>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.</b></p><p><b>#Li-LinkedIn</b></p><p>Job Type: Full-time</p></div>","company":{"companyType":"Public/Established","name":"Aurora Cannabis","logoUrl":"/logos/aurora-cannabis-5846417b31dc1080e3c3b4583c3f2096.png"},"location":{"country":"Canada","address":"Markham, ON","city":"Markham","stateProvince":"ON"},"frontendLink":"/job-posting/aurora-cannabis/quality-assurance-associate/0f5ea7d3161896e8717e47a9b45fe966","title":"Quality Assurance Associate","hash":"0f5ea7d3161896e8717e47a9b45fe966","postingUrl":"https://ca.indeed.com/job/quality-assurance-associate-3a8ad65bf9a0d896"},{"employmentType":"Full-time","postedOn":"11 days ago","description":"<div><p><b>Job Description</b></p><p><b>COMPANY OVERVIEW</b></p><p>Recently named one of Entrepreneur magazines Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods (CPG) approach to cannabis, Crescos house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindys, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Crescos national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industrys first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.</p><p><b>MISSION STATEMENT</b></p><p>At Cresco, we aim to lead the nations cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.</p><p><b>JOB SUMMARY</b></p><p>Cresco Labs is seeking a Quality Assurance (QA) Specialist to join our cultivation facility in Yellow Springs, OH. As a QA Specialist, you will be responsible for assisting with quality-related activities at the facility associated with sampling and inspection of finished products, customer complaints, product investigations, and Corrective and Prevention Action (CAPA). Product families include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges, transdermal patches). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.</p><p><b>CORE JOB DUTIES</b></p><p>• Performs finished product sampling and inspection.</p><p>• Performs equipment and product line clearances before production runs.</p><p>• Inspects retain samples and customer return samples, as deemed necessary.</p><p>• Writes customer complaints and product investigations, helping to assess risk, identify root cause, CAPA plans, and implementing solutions with business partners.</p><p>• Writes QMS documents, including routing and/or approval of change request packages, as requested.</p><p>• Inspects packaged orders to ensure correct content and quantities, as deemed necessary.</p><p>• Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.</p><p>• Reviews in-process batch documentation, logbooks, test results, and good documentation practices.</p><p>• Performs reviews and audits as assigned.</p><p>• Collaborates with operational functions to troubleshoot manufacturing and production defects, CAPA, and customer complaints. Provides advice with process improvements to eliminate errors and reduce risk.</p><p>• Consolidates technical information from operations and manufacturing personnel and prepares written investigation and CAPA reports which may be provided to state regulators. Discuss quality-related issues with state regulators, as needed.</p><p>• Monitors compliance to established Good Manufacturing Practice (GMP) guidance.</p><p>• Executes action plans for product quarantine, destruction, rework, withdrawal/recall.</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• Performs reviews and audits as assigned.</p><p>• Collaborates with operational functions to troubleshoot manufacturing and production defects, CAPA, and customer complaints. Provides advice with process improvements to eliminate errors and reduce risk.</p><p>• May require travel to other states or facilities to perform training and/or assist with quality issues.</p><p>REQUIRED EXPERIENCE, EDUCATION AND SKILLS</p><p>• Bachelors degree or equivalent experience, a plus</p><p>• 3-5 years experience in a quality-focused role required</p><p>• Prior experience in highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, experience.</p><p>• Prior experience in Quality Assurance or Quality Control function.</p><p>• Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA.</p><p>• Prior experience in regulatory agency audits and correspondence.</p><p>• Ability to follow written procedures and monitor others for adherence to written procedures.</p><p>• Ability to create or update written procedures with site operations personnel.</p><p>• Strong written and verbal communication skills.</p><p>• Detail-oriented.</p><p>• Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions.</p><p>• Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.</p><p><b>ADDITIONAL REQUIREMENTS</b></p><p>• Must be 21 years of age or older to apply</p><p>• Must comply with all legal or company regulations for working in the industry</p></div>","company":{"website":"crescolabs.com","companyType":"Public/Established","name":"Cresco Labs","logoUrl":"/logos/cresco-labs-af2becc596b572034007bd7a7d918bdd.png"},"location":{"country":"United States","address":"Yellow Springs, OH, USA","city":"Yellow Springs","stateProvince":"OH"},"frontendLink":"/job-posting/cresco-labs/quality-assurance-specialist/5b6278686a2e233531ee1b16c873eabc","title":"Quality Assurance Specialist","hash":"5b6278686a2e233531ee1b16c873eabc","postingUrl":"https://www.snagajob.com/jobs/641406377"},{"postedOn":"17 days ago","description":"<div><div><p>Central Coast Cannabis Company is looking for an experienced QC Supervisor.</p><p>Quality Control Supervisor assesses production process, and recommends improvements. They are responsible for testing product accuracy.</p><ul><li>PCQI, HACCP, or Equivalent Food Safety Certifications</li></ul><ul><li>Experience in managing GFSI schemes(SQF, ISO90001, AIB, FSSC, BRC)</li></ul><ul><li>Bachelor Degree of Science preferably in Food Science or related field (Meat Science, Biology, Microbiology, Food Microbiology, etc.) or at least 5 years of work experience as quality assurance auditor/technician in dietary supplements, food/beverage, pharmaceutical or cosmetic industry and at least one (1) year of experience in a supervisory capacity.</li></ul><ul><li>A good knowledge of Current Good Manufacturing Practices, preferably 21 CFR Part 111, and food safety.</li></ul><ul><li>Good understanding of quality testing within the food and beverage industry to include analytical, microbiological and sensory evaluation. Must possess a basic understanding of chemical and microbiological analysis and basic math.</li></ul><ul><li>Ability to work under pressure (in an extremely fast paced environment),</li></ul><ul><li>meet deadlines (overtime work required) and make effective decisions.</li></ul><ul><li>Basic computer knowledge (Microsoft Office applications) and computer-based applications).</li></ul><ul><li>Ability to adapt to changing organizational and operational needs; ability to lead others through change.</li></ul><ul><li>Ability to handle multiple tasks simultaneously.</li></ul><ul><li>Skill in organization and prioritization, and attention to details.</li></ul><ul><li>Strong team player and leader with the ability to work across multiple functions and disciplines.</li></ul><ul><li>Must be able to effectively communicate ideas (verbally and in writing), be a self-starter and handle difficult reporting situations.</li></ul></div></div>","company":{"companyType":"Private/Established","name":"SelectStaffing","logoUrl":"/logos/select-staffing-70c544deb6879b17705615399a069575.png"},"location":{"country":"United States","address":"Buellton, CA 93427","city":"Buellton","stateProvince":"CA"},"frontendLink":"/job-posting/selectstaffing/quality-control-supervisor/0683da57ecdae4993bf48787d1953739","title":"Quality Control Supervisor","hash":"0683da57ecdae4993bf48787d1953739","postingUrl":"https://www.indeed.com/job/quality-control-supervisor-94b6a6f22dbfa9fa"},{"postedOn":"17 days ago","description":"<div><div><div><b>Quality Control Associate - Leamington ON.</b></div><div><b>Monday-Friday 8:00AM-4:30PM</b></div><div></div><div><b><i>About Tilray</i></b></div><div><i>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.</i></div><div><i>Looking to develop your career at the forefront of a rapidly expanding industry?</i></div><div></div><div><b>Job Summary:</b></div><div>Reporting to the <b>Quality Control Manage</b>r, the Quality Control Associate is responsible for supporting the Quality Control department by performing a wide range of laboratory tasks including sample weighing, reagent preparation, and data entry. This position will take place at our facility in <b>Leamington ON</b>. and the hours of work will be <b>Monday-Friday 8:00AM-4:30PM.</b></div><div></div><div><b>Your day-to-day responsibilities will consist of:</b></div><ul><li>Ensure a high level of accuracy in sample weighing and reagent preparation.</li><li>Login samples and maintain QC sample database as required.</li><li>Document test results, calculations, and observations as per established SOPs.</li><li>Follow laboratory safety rules and regulations.</li><li>Identifies and communicates non-conformances to Quality Control Supervisor and/or Manager.</li><li>Dispose of analyzed samples and follow proper chemical and waste procedures.</li><li>Ensure laboratory cleanliness is maintained.</li><li>Ensure the integrity and traceability of all generated and reported data.</li><li>Complete logs and records as required.</li><li>Submit samples for testing at third party laboratories as required.</li><li>Input data to laboratory computer software.</li><li>Generate Certificate of Analysis for product release.</li><li>Update ERP system to reflect laboratory inventory changes.</li><li>Administrative duties including data entry, scanning, filling, etc.</li><li>Perform any related tasks assigned by the Quality Control Supervisor and/or Manager</li></ul><div><div><b>To be successful in this position you will have the following:</b></div><ul><li>Post secondary education in a related field required.</li><li>Previous experience in a similar role strongly preferred.</li><li>Strong attention to detail and organizational skills required.</li><li>Ability to read and follow documents (Standard Operating Procedures)</li><li>Knowledge of cGMP requirements or GPP requirements an asset.</li><li>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.</li><li>It is a requirement that the selected Candidate be legally eligible to work in Canada at the time an offer is presented</li></ul><div><b>Internal Candidates:</b> 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</div><div></div><div><b>Note:</b> <i>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.</i> <i>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.</i></div></div></div></div>","company":{"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-control-associate/f10c04e2510aac496d68cd622aa81aa4","title":"Quality Control Associate","hash":"f10c04e2510aac496d68cd622aa81aa4","postingUrl":"https://ca.indeed.com/job/quality-control-associate-b1ec773d4e5bf63f"},{"employmentType":"Full-time, Permanent","postedOn":"21 days ago","description":"<div><p><b>Quality Assurance (QA) Technician | Job Description</b></p><p>The Quality Assurance Technician reports directly to the Head of Cultivation Quality and is responsible for ensuring that the product meets the company's objectives for purity, quality and security. The QA Technician must meet external and internal regulatory requirements including legal compliance and customer expectations. Will be primarily responsible for the monitoring and quality control of cannabis production. The role will also be responsible for ensuring compliance with our Standard Operating Procedures (SOPs).</p><p>We believe all staff must champion organizational culture. We are a customer focused, community conscious, consumer obsessed, no bullsh*t company. We are not a collection of individuals, we are a team that is bound together by our shared values of community, accountability, hard work, dedication and perseverance.</p><p>The QA Technician will report directly to the Head of Cultivation Quality, or designate, and will have no direct reports. In the event of absence, another member of the QA Team will provide coverage.</p><p><b>Core Competencies</b></p><ul><li>Planning and Organizing</li><li>Quality Orientation</li><li>Enforcing Rules and Regulations</li><li>Problem Solving</li><li>Communication</li><li>Accountability and Dependability</li><li>Results Orientation</li><li>Ethics and Integrity</li></ul><p><b>Job Duties</b></p><ul><li>Review, maintain and new or revised Standard Operating Procedures for site facility</li><li>Preparation of batch reports to ensure Cannabis is produced as per GPP/GMP (Good Production Practices/Good Manufacturing Practices)</li><li>Equipment verification and calibration</li><li>Communicate with other managers for process improvements and alignments of quality concepts</li><li>Ensures that all processing activities are carried out as per Standard Operating Procedures to produce consistent quality cannabis products</li><li>Ensures all technical documents in use are current and all master documents such as policy documents and Standard Operating Procedures are controlled and secured in accordance with GMP</li><li>Establish and maintain record keeping systems and ensure employee adherence to proper documentation practices</li><li>Responsible for planning, implementing and managing compliance of manufacturing and production process with internal and external safety, quality and regulatory standards/requirements for distribution</li><li>Implements quality systems in regulated environments to make effective and strategic decisions as a result of evidence-based analysis, striking a balance between quality, productivity and customer service</li><li>Investigate deviations and out of spec results</li><li>Review and approve incoming materials</li><li>Review quality complaints and lead investigations including corrective action and preventive action</li><li>Oversee premises, hygiene of personnel, equipment cleanliness and maintenance</li><li>Implementation of standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of products</li><li>Assure compliance to in-house and external specifications and standards</li><li>Perform internal audits and vendor evaluation audits on a regular basis to determine quality qualifications. Actively participate in external audits such as regulatory inspections.</li><li>Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary</li><li>Assist product support areas in gathering and analyzing data</li><li>Collaborate with other departments to ensure compliance with regulations</li><li>Communicate effectively to all levels of management</li><li>Ability to apply quality concepts and quality processes, including statistical basics and cost of quality</li><li>Other duties as assigned</li></ul><p><b>Requirements</b></p><ul><li>Minimum Bachelor’s Degree in Biological Sciences/Pharmacy/Food or post-secondary diploma in Science related technical discipline</li><li>Experience with GPP, GMP, ISO or any other quality accreditation</li><li>Minimum of 1+ years experience in Quality Assurance</li><li>Experience in the cannabis industry preferred, food safety and/or pharmaceutical experience considered an asset</li><li>Experience operating in a fast-paced organizational environment</li><li>Pesticide safety certification considered an asset</li><li>Previous direct responsibility for determining the strategy to meet quality objectives with the available resources as well as tactile execution</li><li>Must be able to complete a Criminal Background Check</li></ul><p><b>Work Conditions</b></p><p>This role requires a company-provided uniform and additional Personal Protective Equipment to be worn when completing duties and checks in the production area of the facility.</p><ul><li>Office setting</li><li>Repetitive work</li><li>Manual dexterity</li><li>Overtime as required</li></ul><p><b>Health and Safety at Trichome JWC Acquisition Corp.</b></p><p>TJAC is committed to the health and safety of all staff, contractors, consultants or visitors to the facilities. We believe that the well-being of the organization is dependent on the health and safety of our workforce and commit that every precaution reasonable in all circumstances will be taken for the protection of everyone in our facilities.</p><p>TJAC has developed a comprehensive health and safety program that will be reviewed and updated on an annual basis at minimum. Health and safety are essential components of orientation practices. It is the duty of all staff to understand and follow all safety procedures at all times, and to report any unsafe conditions or behaviors as soon as they are identified. This will help the organization to respond, assess, reduce or correct the unsafe condition. Please do not hesitate to ask clarifying questions at any time if needed.</p><p>Because health and safety are highly regarded, any willful infractions will be subject to progressive discipline policies up to an including termination of employment depending on the severity.</p><p>Job Types: Full-time, Permanent</p><p>Salary: From $50,000.00 per year</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Extended health care</li><li>On-site parking</li><li>Paid time off</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>COVID-19 considerations:<br />All precautions are being taken, such as: Temp stations, masked facility, PPE required, social distancing, room limits, staggered shifts, etc.</p><p>Education:</p><ul><li>Bachelor's Degree (preferred)</li></ul><p>Experience:</p><ul><li>QA: 1 year (preferred)</li></ul></div>","company":{"companyType":"Startup","name":"TJAC"},"location":{"country":"Canada","address":"Kitchener, ON","city":"Kitchener","stateProvince":"ON"},"frontendLink":"/job-posting/tjac/quality-assurance-technician/9b7d5addf77a6174306c5eb5ebfe9cf3","title":"Quality Assurance Technician","hash":"9b7d5addf77a6174306c5eb5ebfe9cf3","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-da8feb4ab11fb507"},{"postedOn":"6 days ago","description":"<div><div>Company Description<p><b><br />Join the movement!</b></p><p><b>One of the country’s largest vertically integrated cannabis companies, providing safe, reliable, top-quality cannabis products to improve people’s lives. By investing in people, practices, and infrastructure, we are shaping a new, vital, wellness-focused industry. Our goal is to increase sustainable access to cannabis by offering effective, affordable and trusted products and services.</b></p><p>We are licensed in eight states to grow, process and/or dispense medical cannabis products for adult and pediatric patients, as well as for responsible adult use. We are expanding rapidly as we continue to earn new state licenses and gain recognition as a trusted resource in this evolving space.</p></div><br /><div>Job Description<p><br />With guidance and supervision from the QA Manager and Analyst this position supports the Quality Assurance organization and is responsible for the daily execution of all medical cannabis quality processes as assigned for both operations. The incumbent will work within company standards and the applicable state regulations.</p><p></p><p><b><br />Duties and responsibilities or (Essential Functions)</b></p><p></p><ul><li><br />Under supervision, monitors processes for pre-formulation and finished product manufacturing operations to ensure adherence to company and state regulations; escalating any potential quality issue to the Analyst and/or management immediately</li><li>Assists in product tracking, product security, and product movement procedures.</li><li>Assists in writing, implementing, and training on SOPs for new procedures, critical equipment and processes and/or controls</li><li>Assists in the management of the SOP, investigation, deviation and CAPA systems</li><li>Assists with internal audits</li><li>Assists in review of batch records</li><li>Monitors and documents the complaint log for finished products</li><li>Responsible for batch reconciliations</li><li>Assists manufacturing in the equipment cleaning procedures prior to production start-up and completion; maintains cleaning validation instrumentation and its calibration and supplies</li><li>Projects a positive image of the organization to employees, customers, industry, and community</li><li>Embodies the culture, values, and tenets of PharmaCann and full support of our purpose, goal, and key objectives</li></ul></div><br /><div>Qualifications<ul><li><br />Education/Experience:</li></ul><p>o High School required, plus 5 years related work experience or Associate’s degree, plus three years related work experience</p><p>o Experience having worked in a cannabis and/or manufacturing environment strongly preferred</p><p></p><ul><li><br />Age: State law requires that applicants be 21 years old to work for a cultivation center</li><li>Certifications: None</li></ul><p></p><p><b><br />Working conditions</b></p><p></p><p><br />Work in a manufacturing environment.</p><p></p><p><b><br />Physical requirements</b></p><p></p><p><br />This job may be required to stand and/or walk for long periods of time and occasional lifting up to 50 pounds.</p><br />Additional Information<p><br />All your information will be kept confidential according to EEO guidelines.</p><p>PharmaCann, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age disability or genetics. We value diversity, military service, and law enforcement experience. Compensation is competitive and will be commensurate with experience. Benefits are available.</p></div></div>","company":{"companyType":"Established","name":"PharmaCannis"},"location":{"country":"United States","address":"Hamptonburgh, NY","city":"Hamptonburgh","stateProvince":"NY"},"frontendLink":"/job-posting/pharmacannis/ny-quality-assurance-specialist/1c4e4de79a46b808016ff3810442194f","title":"NY - Quality Assurance Specialist","hash":"1c4e4de79a46b808016ff3810442194f","postingUrl":"https://www.indeed.com/job/ny-quality-assurance-specialist-6d12312e9c5210ee"},{"employmentType":"Full-time","postedOn":"22 days ago","description":"<div><p>Who we are</p><p>Here at Vireo Health, Inc. (\"Vireo\") our mission is to bring the best of technology, science, and engineering to the cannabis industry. We are a physician-led, customer-focused team of more than 500 dedicated employees creating best-in-class cannabis products and customer experiences. Vireo is proud to have one of the most diverse workforces in cannabis, promoting diversity, equity, and inclusion through engaging employee outreach programs, community events, and non-profit partnerships. We are rapidly expanding nationwide, and we are looking for talented, compassionate, and dedicated people to join our team and help us grow. From Cultivation to Operations to Sales &amp; Marketing, we are hiring people who share our vision and passion for improving people's lives. If you are looking for a positive work environment where your contributions truly make a difference, click apply and let us learn about you!</p><p>We are seeking an energetic and dedicated Quality Assurance Specialist to join our growing dynamic team. The Quality Assurance Specialist is responsible for quality inspections of Medical Cannabis products and monitoring the processes and procedures in the medical cannabis manufacturing operation. This individual will be required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), Good Laboratory Practice (GLP) and other product quality standards. The Quality Assurance Specialist will assists in aligning the company with all state, federal and 3rd party requirements. Compliance will work with QA to ensure compliance with government regulatory agencies and third-party audits. This role reports directly to the Quality Manager.</p><p>Highlighted Responsibilities</p><p>• Perform Quality Control inspections on products, equipment, processes and procedures.</p><p>• Ensure package integrity and accuracy.</p><p>• Responsible for monitoring product cannabis safety and quality throughout the manufacturing process.</p><p>• Ensure all cannabis and cannabis containing products produced at the facility are properly tested in accordance with company and State procedures and guidelines, at appropriate frequencies, and meet specifications prior to release.</p><p>• Ensure testing data is appropriately recorded and maintained.</p><p>• Responsible for performing verification on equipment and other areas required.</p><p>• Responsible for ensuring the correct recording and filing of all relevant record logs and documentation completed by staff.</p><p>• Ensures the correct guidelines for production are followed during operations.</p><p>• Ensures all employees are following all SOPs, Work Instructions and worker safety practices.</p><p>• Assist Quality Manager and/or Director of Quality and Product Safety with instructing employees on quality improvements and issues.</p><p>• Analyze quality data to recommend quality and process improvements.</p><p>• Collect product samples for product development, lab retains and the laboratory when directed.</p><p>• Support the Quality team as needed.</p><p><b>Qualifications</b></p><p>• High School Diploma required; must be at least 21 years old</p><p>• 2 years minimum employment experience in a manufacturing/quality control setting</p><p>• Bilingual (English/Spanish) is preferred</p><p>• Experience with record keeping/internal auditing</p><p>• Ability to follow existing inventory/inspection procedures accurately</p><p>• Working knowledge of general computer operation and competency with Microsoft Office Products</p><p>• Experience operating in a quality-centric setting (Medical/Manufacturing/Health related industries)</p><p>• Good writing/reading/arithmetic skills</p><p>• Basic physical ability to walk back and forth across facility (could be outdoors) and lift/move up to 50lbs if necessary</p><p>• Self-motivated with proven leadership skills and attention to detail</p><p>• Strong interpersonal skills for multitasking and interacting with team members</p><p>EEO Statement</p><p>Vireo Health, Inc. is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. www.vireohealth.com</p><p>Accessibility: If you need an accommodation as part of the employment process please contact Human Resources at</p><p>Email: [email protected]</p></div>","company":{"website":"goodnessgrowth.com","companyType":"Private/Established","name":"Vireo Health","logoUrl":"/logos/vireo-health-125544955cfe8cdd68bc5cddd679f996.png"},"location":{"country":"United States","address":"Otsego, MN, USA","city":"Otsego","stateProvince":"MN"},"frontendLink":"/job-posting/vireo-health/quality-assurance-specialist/3475d1f1f7f8bcb995370d2426de5c5d","title":"Quality Assurance Specialist","hash":"3475d1f1f7f8bcb995370d2426de5c5d","postingUrl":"https://getwork.com/details/603b09dac574fefd74e8bb2175eaccc3"},{"employmentType":"Full-time","postedOn":"23 days ago","description":"<div><p>Who we are</p><p>Here at Vireo Health, Inc. (\"Vireo\") our mission is to bring the best of technology, science, and engineering to the cannabis industry. We are a physician-led, customer-focused team of more than 500 dedicated employees creating best-in-class cannabis products and customer experiences. Vireo is proud to have one of the most diverse workforces in cannabis, promoting diversity, equity, and inclusion through engaging employee outreach programs, community events, and non-profit partnerships. We are rapidly expanding nationwide, and we are looking for talented, compassionate, and dedicated people to join our team and help us grow. From Cultivation to Operations to Sales &amp; Marketing, we are hiring people who share our vision and passion for improving people's lives. If you are looking for a positive work environment where your contributions truly make a difference, click apply and let us learn about you</p><p>We are seeking an energetic and dedicated Quality Assurance Specialist to join our growing dynamic team. The Quality Assurance Specialist is responsible for quality inspections of Medical Cannabis products and monitoring the processes and procedures in the medical cannabis manufacturing operation. This individual will be required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), Good Laboratory Practice (GLP) and other product quality standards. The Quality Assurance Specialist will assists in aligning the company with all state, federal and 3rd party requirements. Compliance will work with QA to ensure compliance with government regulatory agencies and third-party audits. This role reports directly to the Quality Manager.</p><p>Highlighted Responsibilities</p><p>• Perform Quality Control inspections on products, equipment, processes and procedures.</p><p>• Ensure package integrity and accuracy.</p><p>• Responsible for monitoring product cannabis safety and quality throughout the manufacturing process.</p><p>• Ensure all cannabis and cannabis containing products produced at the facility are properly tested in accordance with company and State procedures and guidelines, at appropriate frequencies, and meet specifications prior to release.</p><p>• Ensure testing data is appropriately recorded and maintained.</p><p>• Responsible for performing verification on equipment and other areas required.</p><p>• Responsible for ensuring the correct recording and filing of all relevant record logs and documentation completed by staff.</p><p>• Ensures the correct guidelines for production are followed during operations.</p><p>• Ensures all employees are following all SOPs, Work Instructions and worker safety practices.</p><p>• Assist Quality Manager and/or Director of Quality and Product Safety with instructing employees on quality improvements and issues.</p><p>• Analyze quality data to recommend quality and process improvements.</p><p>• Collect product samples for product development, lab retains and the laboratory when directed.</p><p>• Support the Quality team as needed.</p><p><b>Qualifications</b></p><p>• High School Diploma required; must be at least 21 years old</p><p>• 2 years minimum employment experience in a manufacturing/quality control setting</p><p>• Bilingual (English/Spanish) is preferred</p><p>• Experience with record keeping/internal auditing</p><p>• Ability to follow existing inventory/inspection procedures accurately</p><p>• Working knowledge of general computer operation and competency with Microsoft Office Products</p><p>• Experience operating in a quality-centric setting (Medical/Manufacturing/Health related industries)</p><p>• Good writing/reading/arithmetic skills</p><p>• Basic physical ability to walk back and forth across facility (could be outdoors) and lift/move up to 50lbs if necessary</p><p>• Self-motivated with proven leadership skills and attention to detail</p><p>• Strong interpersonal skills for multitasking and interacting with team members</p><p>EEO Statement</p></div>","company":{"website":"goodnessgrowth.com","companyType":"Private/Established","name":"Vireo Health","logoUrl":"/logos/vireo-health-125544955cfe8cdd68bc5cddd679f996.png"},"location":{"country":"United States","address":"Otsego, MI, USA","city":"Otsego","stateProvince":"MI"},"frontendLink":"/job-posting/vireo-health/quality-assurance-specialist/58ac106c4cb1803f9d7ba48d3311b33c","title":"Quality Assurance Specialist","hash":"58ac106c4cb1803f9d7ba48d3311b33c","postingUrl":"https://us.bebee.com/job/20210707-6ae4cd9c1e2f20ff4d9140fa6488d3e0"},{"employmentType":"Full-time","postedOn":"24 days ago","description":"<div><p>Our client, startup Cannabis Testing Laboratory based in Santa Barbara, is searching for a Quality Assurance Specialist with previous Cannabis Industry experience to join their growing team.</p><p>In this role, the successful applicant will be responsible for overseeing the quality assurance responsibilities for their new Cannabis Testing Laboratory to ensure the utmost in customer satisfaction.</p><p>The Quality Assurance Specialist will also be responsible for ensuring continual quality improvement within the facility. If you have a strong background in quality management and exceptional leadership abilities, we encourage you to apply.</p><p><b>Job Duties and Responsibilities:</b></p><p>• Establish QMS policy, procedures and report to management on the performance.</p><p>• Responsible for accuracy and timely inspections on all instruments in the testing laboratory.</p><p>• Help guide the company through the BCC licensing process</p><p>• Assist the CSO and Laboratory Directors through the ISO:17025 accreditation process</p><p>• Become the day to day contact/support with the BCC</p><p>• Implement a Quality Control system within the organization</p><p>• Successful completion of proficiency testing samples and initial demonstration of capability to demonstrate competence as required for certifications or customer requests.</p><p>• Ensure existing procedures and the drafting of new procedures under the supervision of the Laboratory Manager.</p><p><b>Preferred Skills and Requirements:</b></p><p>• Cannabis experience strongly preferred</p><p>• Bachelor's degree in related field</p><p>• 2+ years of quality management experience</p><p>• 2-3+ years of analytical laboratory experience</p><p>• Proficiency with laboratory testing instruments</p><p>• Impeccable communication, presentation and organizational skills</p><p>• Experience with Quality Management Systems and data review</p><p>• Proficient in computer technology and Microsoft Office</p><p>• Ability to work in a team environment</p><p>• ISO 17025 experience</p><p>• Excellent analytical and problem solving skills</p><p>Salary: $60,000 - $65,000 Plus Benefits</p><p>If this sounds like the cannabis industry position you have been waiting for, please apply using the online application or the link below - all inquiries are strictly confidential. Our focus is to assist you to make your best next career move, and we will not use your information for any other purpose.</p><p>CannabizTeam is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. TEAM100</p><p>www.CannabizTeam.com</p></div>","company":{"companyType":"Private/Growth","name":"CannabizTeam","logoUrl":"/logos/cannabizteam-71e68432a5b2ab7a22442dc51667849a.jpeg"},"location":{"country":"United States","address":"Santa Barbara, CA, USA","city":"Santa Barbara","stateProvince":"CA"},"frontendLink":"/job-posting/cannabizteam/quality-assurance-specialist/b1c4c1f8ed90bc0c421752aa307f1a42","title":"Quality Assurance Specialist","hash":"b1c4c1f8ed90bc0c421752aa307f1a42","postingUrl":"https://cannabisjobs.net/job/47156/quality-assurance-specialist/"},{"employmentType":"Full-time, Permanent","postedOn":"22 days ago","description":"<div><p><b>Scope of Responsibility/Primary Objectives: </b></p><ul><li>Full-time position, based in Mount Albert, Ontario</li><li>Ensure that all processing activities are carried out in accordance with the Standard Operating Procedures (SOP), to result in consistent highest quality cannabis products.</li><li>Collaborate with finance, accounting, CRA, Health Canada and wholesale customers on monthly reports in a timely manner.</li><li>Collaborate with other relevant departments including Production and Operations to ensure compliance with Health Canada regulations and guidelines, adhering to the Cannabis Act.</li><li>Must ensure that all technical documents at 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.</li><li>Responsible for managing and coordinating QA staff, creating department efficiencies, and providing leadership support.</li><li>Must be able to communicate effectively to all levels of the organization and assist in training of employees.</li><li>Implementation of standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products.</li><li>Responsible for planning, implementing, and managing compliance of manufacturing and production process with internal and external safety, quality and regulatory standards/requirements for worldwide distributions.</li><li>Assures compliance to in-house and/or external specifications and standards, such as GMP, GGP, GPP, GDP, Cannabis Act.</li><li>Design methods and procedures for inspecting testing and evaluating the precision and accuracy of production processes, production equipment and finished products.</li><li>Perform internal audits, and vendor evaluation audits on regular basis to determine quality qualifications.</li><li>Actively participate in external audits conducted such as Health Canada Inspections, OH &amp; S inspections.</li><li>Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary.</li><li>Assist product support areas in gathering and analyzing data.</li><li>Participate in the reviewing of engineering designs to contribute quality requirements and considerations.</li><li>Assistance with Inventory &amp; stock handling / shipping / receiving and organization to SOP’s.</li><li>Maintain regular collaborative communication with Lead Growers.</li><li>Understand, and follow all SOPs and related forms to GMP standards.</li><li>Complete all required documentation using good documentation practices.</li><li>Attend and participate in production and management meetings (as required).</li><li>Other related support duties as assigned to maintain efficient business operations.</li></ul><p><b>Education, Experience, Qualifications and Skills</b></p><ul><li>Must have valid Health Canada security clearance in the cannabis industry.</li><li>2-5 years (min.) experience in facilitating Health Canada audits</li><li>Previous experience with inspecting methods in the design and production of c'annabis an asset.</li><li>Project planning and management capabilities, experience with change management.</li><li>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.</li><li>Strong team player with the ability to conduct work with confidentiality and professionalism.</li><li>Ability to prioritize and organize a changing workload while maintaining a high level of integrity and accuracy. Ability to work under pressure and to scheduled deadlines.</li><li>Self-starter with the ability to identify problems and then develop and implement solutions.</li><li>Strong analytical skills and problem-solving skills.</li><li>Ability to develop reporting in an efficient and effective manner.</li><li>Ability to multi-task in a rapidly changing environment.</li><li>Experience in using cannabis tracking technology; including Ample Organics, CTLS Reporting system.</li><li>Proficiency in Office 365, particularly Word, Excel, Power Point, Teams, etc.</li><li>Accountable for QA department results, strives to meet and exceed expectations.</li><li>Strong written, verbal and communication skills.</li><li>Be positive, energetic and comfortable in an open, dynamic and collaborative company culture.</li><li>Have previous working experience in a highly regulated production environment such as cannabis, pharmaceuticals, medical devices, food/beverage, cosmetics, etc.</li><li>Experience specific to the cannabis industry with understanding of other cannabis business operational areas.</li><li>Proficient in English, with excellent oral and written communication skills.</li><li>First aid certified and WHMIS certified is an asset.</li></ul><p>Application Deadline: 2021-07-19</p><p>Expected Start Date: 2021-07-22</p><p>Job Types: Full-time, Permanent</p><p>Salary: $75,000.00 per year</p><p>Benefits:</p><ul><li>On-site parking</li><li>Paid time off</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>COVID-19 considerations:<br />- All employees are expected to wear masks<br />- Common areas are sanitized regularly</p><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Startup","name":"STRAINS Ltd"},"location":{"country":"Canada","address":"Mount Albert, ON","city":"Mount Albert","stateProvince":"ON"},"frontendLink":"/job-posting/strains-ltd/quality-assurance-person-qap/326afc5cd3cc96c47dc42f72f8e6fc2a","title":"Quality Assurance Person - QAP","hash":"326afc5cd3cc96c47dc42f72f8e6fc2a","postingUrl":"https://ca.indeed.com/job/quality-assurance-person-qap-432b5603d78bee31"},{"employmentType":"Full-time","postedOn":"24 days ago","description":"<div><p>Who we are</p><p>Here at Vireo Health, Inc. (\"Vireo\") our mission is to bring the best of technology, science, and engineering to the cannabis industry. We are a physician-led, customer-focused team of more than 500 dedicated employees creating best-in-class cannabis products and customer experiences.Vireo is proud to have one of the most diverseworkforces in cannabis, promoting diversity, equity, and inclusion through engaging employee outreach programs, community events, and non-profit partnerships. We are rapidly expanding nationwide, and we are looking for talented, compassionate, and dedicated people to join our team and help us grow. From Cultivation to Operations to Sales &amp; Marketing, we are hiring people who share our vision and passion for improving people's lives. If you are looking for a positive work environment where your contributions truly make a difference, click apply and let us learn about you!</p><p>We are seeking an energetic and dedicated Quality Assurance Specialist to join our growing dynamic team. The Quality Assurance Specialist is responsible for quality inspections of Medical Cannabis products and monitoring the processes and procedures in the medical cannabis manufacturing operation. This individual will be required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), Good Laboratory Practice (GLP) and other product quality standards. The Quality Assurance Specialist will assists in aligning the company with all state, federal and 3rd party requirements. Compliance will work with QA to ensure compliance with government regulatory agencies and third-party audits. This role reports directly to the Quality Manager.</p><p>Highlighted Responsibilities</p><p>Perform Quality Control inspections on products, equipment, processes and procedures.</p><p>Ensure package integrity and accuracy.</p><p>Responsible for monitoring product cannabis safety and quality throughout the manufacturing process.</p><p>Ensure all cannabis and cannabis containing products produced at the facility are properly tested in accordance with company and State procedures and guidelines, at appropriate frequencies, and meet specifications prior to release.</p><p>Ensure testing data is appropriately recorded and maintained.</p><p>Responsible for performing verification on equipment and other areas required.</p><p>Responsible for ensuring the correct recording and filing of all relevant record logs and documentation completed by staff.</p><p>Ensures the correct guidelines for production are followed during operations.</p><p>Ensures all employees are following all SOPs, Work Instructions and worker safety practices.</p><p>Assist Quality Manager and/or Director of Quality and Product Safety with instructing employees on quality improvements and issues.</p><p>Analyze quality data to recommend quality and process improvements.</p><p>Collect product samples for product development, lab retains and the laboratory when directed.</p><p>Support the Quality team as needed.</p><p><b>Qualifications</b></p><p>High School Diploma required; must be at least 21 years old</p><p>2 years minimum employment experience in a manufacturing/quality control setting</p><p>Bilingual (English/Spanish) is preferred</p><p>Experience with record keeping/internal auditing</p><p>Ability to follow existing inventory/inspection procedures accurately</p><p>Working knowledge of general computer operation and competency with Microsoft Office Products</p><p>Experience operating in a quality-centric setting (Medical/Manufacturing/Health related industries)</p><p>Good writing/reading/arithmetic skills</p><p>Basic physical ability to walk back and forth across facility (could be outdoors) and lift/move up to 50lbs if necessary</p><p>Self-motivated with proven leadership skills and attention to detail</p><p>Strong interpersonal skills for multitasking and interacting with team members</p><p>EEO Statement</p><p>Vireo Health, Inc. is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. www.vireohealth.com</p></div>","company":{"website":"goodnessgrowth.com","companyType":"Private/Established","name":"Vireo Health","logoUrl":"/logos/vireo-health-125544955cfe8cdd68bc5cddd679f996.png"},"location":{"country":"United States","address":"Albertville, MN, USA","city":"Albertville","stateProvince":"MN"},"frontendLink":"/job-posting/vireo-health/quality-assurance-specialist/15c3e5e9c6e3d0426f91f1a2a05649e9","title":"Quality Assurance Specialist","hash":"15c3e5e9c6e3d0426f91f1a2a05649e9","postingUrl":"https://www.ziprecruiter.com/c/Vireo-Health/Job/Quality-Assurance-Specialist/-in-Albertville,MN?jid=47e96c34e67cfd20"},{"employmentType":"Full-time","postedOn":"1 day ago","description":"<div><p>The Quality Assurance Specialist supports the Team in the verification and validation of quality assurance, ensuring that cannabis products produced meet the organization's objectives for quality, safety, regulatory, and customer expectations in accordance with the Cannabis Act &amp; relevant regulations. The Quality Assurance Specialist will maintain and monitor Quality Management Systems and coordinate activities to meet production process and product quality standards.</p><p><b>Responsibilities:</b></p><p>• Assist in managing the licensed sites Quality Assurance Department and assist in developing, reviewing, and maintaining SOPs &amp; Quality Management Programs and projects to ensure compliance under the Cannabis Act/Regulations.</p><p>• Work cross-departmentally to implement &amp; maintain SOPs (i.e. Operations, Regulatory, Security);</p><p>• Maintain QMS by performing record-keeping tasks such as document updates</p><p>• Collect and review production Quality documents (sanitation journals, maintenance work orders, etc);</p><p>• Develop and execute a Sanitation Verification system using ATP swab collection;</p><p>• Support release of products through batch record compilation and review;</p><p>• Perform review, inspection, and/or validation of new materials and equipment; and</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>• MUST HAVE previous Cannabis Industry QA Experience;</p><p>• Active HC Security Clearance is a STRONG asset;</p><p>• BSc Degree in Chemistry, Biology, Pharmacology or Food Science, obtained or recognized by a Canadian University;</p><p>• 2+ 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>• Valid security clearance (ACMPR or Cannabis Regulations) is a strong asset;</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":"Delta, BC","city":"Delta","stateProvince":"BC"},"frontendLink":"/job-posting/cannabis-at-work/quality-assurance-specialist-cannabis-cultivation/faab8e42f6bde25abb7108125003b0a9","title":"Quality Assurance Specialist (Cannabis Cultivation)","hash":"faab8e42f6bde25abb7108125003b0a9","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-specialist-cannabis-cultivation-at-cannabis-at-work-2660112096"},{"employmentType":"Contractor","postedOn":"17 days ago","description":"<div><p><b>The Company</b></p><p>At Canopy Growth, our mission is clear: improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We're building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.</p><p>With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.</p><p>Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you</p><p><b>The Opportunity</b></p><p>Reporting directly to the Manager, Operational and Product Quality, the QA Specialist is accountable for the development, implementation and ongoing monitoring of the quality assurance and control systems in strict compliance with the Cannabis Act. If you enjoy working in a fast-paced environment, then we want to hear from you</p><p><b>Responsibilities</b></p><p>• Executing and monitoring our internal hold and release procedure</p><p>• Maintaining QA oversight of inventory within our ERP system</p><p>• Reviewing various production documentation for completeness and accuracy while adhering to Good Documentation Practice</p><p>• Monitoring internal task logging software and making changes as required</p><p>• Qualifying new production rooms for use</p><p>• Fulfilling QA tasks for the operations team to ensure production runs smoothly</p><p>• Initiating and completing non-conformity reports and corrective action plans when necessary</p><p>• Collaborate with Quality Control, Regulatory Affairs, Manufacturing and Product Development departments to ensure compliance with Health Canada regulations and guidelines</p><p>• Creating and/or revising standard operating procedures when required</p><p>• Other responsibilities as assigned</p><p><b>Experience</b></p><p>• Degree or diploma in biology, biotechnology, pharmacology or related field (or relevant working experience)</p><p>• 3-5 years' of relevant experience</p><p>• Working knowledge of Good Documentation Practices, Good Manufacturing Practices and Cannabis Regulations as asset</p><p>• Experience reviewing and revising regulated documents</p><p>• Experience working in an ISO:9001 or GMP environment considered an asset</p><p>• Experience in a fast-paced working environment where time management, organization and problem solving were key skills</p><p>• Strong teamwork skills</p><p>• High attention to detail</p><p>• Working knowledge of Microsoft Office suite of programs</p><p>• Experience with ERP systems (Sage or SAP) considered an asset</p><p><b>Other Details</b></p><p>This is a 12-month contract role based out of Smiths Falls, ON.</p><p>We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don't hear from us, don't fret; every resume we get is kept in our database for six months for consideration in future searches for talent.</p><p>Canopy Growth welcomes and encourages applications from people with disabilities.</p><p>Accommodations are available upon request for candidates taking part in all aspects of the selection process.</p><p>One last note: the chosen applicant will be required to successfully complete background and reference checks.</p><p>Thank you so much for your interest in Canopy Growth.</p><p>Apply Now</p><p>• Smiths Falls, ON, Canada</p></div>","company":{"website":"canopygrowth.com","companyType":"Public/Established","name":"Canopy Growth Corp.","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Smiths Falls, ON","city":"Smiths Falls","stateProvince":"ON"},"frontendLink":"/job-posting/canopy-growth-corp/quality-assurance-specialist-contract/8925da02e31088d0ac5a1e26ba33498e","title":"Quality Assurance Specialist - Contract","hash":"8925da02e31088d0ac5a1e26ba33498e","postingUrl":"https://ca.bebee.com/job/20210713-eb8e8b3770fe9b7ddaf739d4dc79b9fb"},{"postedOn":"7 days ago","description":"<div><div>We are looking for an experienced, highly motivated, self-starter Quality Assurance Specialist who is ready to take on a new challenge.<br />Are you looking for an opportunity to work in a large corporation and a lot of growth opportunities?<br />If yes, this could be a great opportunity for you. Work-life balance and great work environment!<br /><br /><br /><b>Advantages</b><br />The ideal candidate will be able to work with a cross-functional team in a fast-paced environment, who will be reporting directly to the QA Management Supervisor.<br />If you have sound judgment mixed with the ability to work as part of an ever-growing team, we want to hear from you!<br /><br /><b>Responsibilities</b><br /><ul><li>Manage quality system processes such as management review and annual product review</li><li>Partners with stakeholders across multiple sites to ensure knowledge sharing and successful implementation of APR, management review and continuous improvement projects</li><li>Management of updates of Quality Manual and Site Master File</li><li>Supporting quality assurance training process</li><li>Supporting Health Canada Inventory process</li><li>Supporting continuous improvement projects</li><li>Other tasks in the Quality Assurance department as required.</li></ul><br /><br /><b>Qualifications</b><br /><ul><li>Bachelor of Science degree or College Technical Diploma from a recognized institution in Biotechnology, Chemistry or Life Sciences preferred</li><li>At least one-year of experience working in a GMP pharmaceutical environment. Individuals with experience in Medical Devices or other highly regulated industries will be considered.</li><li>Ability to work independently or in a team environment</li><li>Detail oriented</li><li>Knowledge of Canadian Cannabis Regulations (SOR/2018-144), Food &amp; Beverage Regulations and the European GMP Regulations. Individuals with experience in Medical devices or other highly regulated industries will also be considered</li><li>Knowledge of Quality Management Systems: CAPA, Change Control, Design Change, Management review, annual product review</li><li>Basic statistical skills</li><li>Knowledge of Outlook, Word, and Excel</li></ul><br /><b>Summary</b><br />If this is the position for you, APPLY ONLINE or email resume to Dawn Urbanowicz at [email protected]<br />Only qualified candidates will be contacted.<br />Please visit www.randstad.ca for a complete list of opportunities</div></div>","company":{"companyType":"Public/Established","name":"Randstad"},"location":{"country":"Canada","address":"Smiths Falls, ON","city":"Smiths Falls","stateProvince":"ON"},"frontendLink":"/job-posting/randstad/quality-assurance-specialist-smiths-falls/dbc0d8a80ad06cee3e4ca76bd06e958f","title":"Quality Assurance Specialist - Smiths Falls","hash":"dbc0d8a80ad06cee3e4ca76bd06e958f","postingUrl":"https://ca.indeed.com/job/quality-assurance-specialist-smiths-falls-ec26b9e89562f650"},{"employmentType":"Full-time","postedOn":"24 days ago","description":"<div><p><b>GMP Quality Assurance Coordinator (Contract) - Leamington ON. Monday-Friday 8:00AM-4:30PM 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. Looking to develop your career at the forefront of a rapidly expanding industry? Job Summary: Reporting to the Quality Assurance Manager - GMP, the Quality Assurance Coordinator – GMP applies in depth knowledge of products, processes and testing methods to ensure safety and efficacy of products. Assists with reviewing results, methods, specifications, environmental monitoring, and NCRs on an ongoing basis and through Annual Product Reviews (APRs). In addition, assists with coordinating/investigating customer complaints, internal audits, and vendor qualifications. This position will be a contract position until November 15th, 2021. Your day-to-day responsibilities will consist of:</b></p><p>• Continuous knowledge and understanding of GMP regulatory requirements as established by</p><p>• Health Canada’s Good Manufacturing Practices (GMP) Guidelines (GUI-0001), Health Canada’s</p><p>• Good Manufacturing Practices (GMP) Guidelines for Active Pharmaceutical Ingredients (API) (GUI0104), and the European Commission’s Eudralex Vol. 4 Good Manufacturing Practice Part II: Basic</p><p>• Requirements for Active Substances used as Starting Materials</p><p>• Assist all functional departments on establishing systems to eliminate GMP gaps</p><p>• Support and maintain systems to ensure quality of products as defined through internal Good</p><p>• Manufacturing Practices and established Standard Operating Procedures</p><p>• Support quality requirements to all operational departments</p><p>• Create, review and maintain Standard Operational Procedures and Raw Material Specifications,</p><p>• investigate non-conformances/deviations and customer complaints as it relates to quality</p><p>• Release or reject Active Pharmaceutical Ingredients (API) and/or other raw material(s)</p><p>• Assist in establishing a system to release or reject Active Pharmaceutical Ingredients (API) and/or</p><p>• other starting material(s)</p><p>• Maintain the internal audit schedule and audit criteria as well as assist with conducting Internal</p><p>• Audits</p><p>• Participate in the initiation, writing, and coordination of change controls to controlled documents</p><p>• as needed to ensure defined quality objectives are met</p><p>• Assist with documenting, reporting, initiating and monitoring corrective actions and preventative actions</p><p>• Assist with coordinating, writing, and investigating non-conformance reports</p><p>• Ensure deviations are investigated and resolved</p><p>• Acts as the primary point of contact for customer complaint investigation and ensures resolution;</p><p>• leads and performs related responsibilities as required</p><p>• Prepares Quarterly Environmental Monitoring Reports, in compliance with SOPs and GMP</p><p>• regulations, as needed</p><p>• Provides services leading to, and inclusive of, preparation of Annual Product Reviews for all</p><p>• products marketed, in compliance with SOPs and GMP regulations</p><p>• Review and release batch production records prior to the release of product</p><p>• Must be able to work extended hours, weekends as needed, especially when problems occur or</p><p>• when deadlines must be met</p><p>• Ensure materials are appropriately tested and the results are reported</p><p>• Assist and/or perform product quality reviews</p><p>• Read, understand and follow safe work procedures</p><p>• Other duties as assigned, provided training has been conducted</p><p>• At least 2 years relevant practical experience is preferred in order to act as the delegated</p><p>• responsible quality person in charge, if required</p><p>• Coordinate annual GMP training and new hire GMP training</p><p>• Manage the qualifications and approval of vendors, contractors and contract labs as required</p><p><b>To be successful in this position you will have the following:</b></p><p>• A bachelor’s degree in a science related field and/or technical Diploma from an accredited postsecondary institution.</p><p>• Quality experience in a pharmaceutical environment is preferred</p><p>• Knowledge and understanding of GMP (Good Manufacturing Practices) is essential</p><p>• Superior communication and writing skills</p><p>• Self-starter, critical thinker and team oriented</p><p>• Ability to lead a team</p><p>• Commitment to continuous professional development</p><p>• Excellent leadership skills, problem solving skills and decision-making skills</p><p>• High work ethic standards are a must</p><p>• Exceptional attention to detail</p><p>• Must have a documented health exam and eye exam demonstrating clearance for working within a</p><p>• GMP environment within two weeks of employment commencement</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 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-coordinator-gmp/3dfae9d0f20f9cb83d5584f44c143ff4","title":"Quality Assurance Coordinator - GMP","hash":"3dfae9d0f20f9cb83d5584f44c143ff4","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-coordinator-gmp-at-tilray-2636576824"},{"postedOn":"17 days ago","description":"<div><div><div><b>Quality Assurance Associate - Cultivation</b><b>- Leamington ON.</b></div><div><b>Monday-Friday </b><b>6:30AM-3:00PM &amp; 3:00PM-11:30PM</b>.</div><div></div><div><b><i>About Tilray</i></b></div><div><i>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.</i></div><div><i>Looking to develop your career at the forefront of a rapidly expanding industry?</i></div><div></div><div><b>Job Summary:</b></div><div>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 &amp; 3:00PM-11:30PM.</div><div></div><div><b>Your day-to-day responsibilities will consist of:</b></div><ul><li>Continually monitor cultivation areas for GPP regulatory requirements under the Cannabis Act and Cannabis Regulations and their associated regulations such as those for Natural Health Products.</li><li>Assist all functional departments on establishing systems to eliminate GACP/GPP gaps that relate to cultivation, harvest and inspection of product.</li><li>Support and maintain systems to ensure quality of products as defined through internal Good Production Practices and established Standard Operating Procedures.</li><li>Communicate, educate and support the quality requirements to all operational departments.</li><li>Create, review and maintain Standard Operational Procedures, investigate non-conformances/deviations and customer complaints as it relates to quality.</li><li>Participate in the initiation and writing of change controls to controlled documents as needed to ensure defined quality objectives are met</li><li>Coordinate and conduct new hire and ongoing GPP/GACP training.</li><li>Read, understand and follow safe work procedures</li><li>Other duties as assigned</li></ul><div><b>To be successful in this position you will have the following:</b></div><ul><li>A combination of bachelor’s degree in science related field and/or technical Diploma from an accredited post-secondary institution.</li><li>Quality experience in a horticulture, food or health product environment is preferred</li><li>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</li><li>Superior communication and writing skills</li><li>Self-starter, critical thinker and team oriented</li><li>High work ethic standards are a must</li><li>Exceptional attention to detail</li><li>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.</li><li>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.</li><li>It is a requirement that the selected Candidate be legally eligible to work in Canada at the time an offer is presented.</li></ul><div><div><b>Internal Candidates:</b> 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</div><div></div><div><b>Note:</b> <i>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.</i> <i>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.</i></div></div></div></div>","company":{"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-cultivation/597ca143eb4de608c1dc8dc33aee730c","title":"Quality Assurance Associate - Cultivation","hash":"597ca143eb4de608c1dc8dc33aee730c","postingUrl":"https://ca.indeed.com/job/quality-assurance-associate-cultivation-df4b087a2ab6fee5"}]