3910 results
Quality Manager Elixinol Broomfield, CO 80021
12 hours ago
Quality Manager Cresco Labs Fall River, MA
5 days ago
Cannabis Quality Manager Cannabis Consulting Group Los Angeles, CA 91406
13 hours ago
Quality Control / Quality Assurance Specialist Cresco Labs Mendota, CA
20 days ago
Cannabis Product Quality Manager Trovaro Chicago, IL, USA (+1 other)
7 days ago
Cannabis Product Quality Manager Trovaro Berwyn Heights, MD
10 days ago
Jooble - Cannabis Product Quality Manager Trovaro Chicago, IL (+1 other)
19 days ago
Quality Assurance Associate Charlottes Web Louisville, CO 80027
12 hours ago
Quality Assurance Associate Adecco Canada Grimsby, ON
2 days ago
Quality Assurance Analyst Blossim Inc. Vaughan, ON
3 days ago
Quality Assurance Supervisor Trulieve Cannabis Tallahassee, FL, USA
4 days ago
Quality Control Technician Aurora Cannabis British Columbia
5 days ago
Quality Control Technician Aurora Cannabis Canada
6 days ago
Quality Control Lead MJardin Group Brampton, ON, Canada
8 days ago
Quality Assurance Person Green House Dispensary Los Angeles, CA, USA (+1 other)
7 days ago
Quality Assurance Person Namaste Technologies Canada
8 days ago
Quality Assurance Technician Canopy Growth Corporation Niagara-on-the-Lake, ON
8 days ago
Director, Quality Assurance Sundial Growers Olds, AB (+1 other)
8 days ago
Quality Assurance Supervisor Charlotte's Web Hemp Louisville, CO
8 days ago
Quality Assurance (QA) Technician JWC Kitchener, ON
8 days ago
Quality Assurance Technician Canopy Growth Corporation Smiths Falls, ON, Canada (+1 other)
9 days ago
Quality Assurance Associate - WMMC Aurora Cannabis Canada
2 days ago
Quality Control Specialist Rubicon Organics Delta, BC, Canada (+1 other)
11 days ago
Web Quality Assurance Canopy Growth Corporation Ottawa, ON, Canada (+1 other)
9 days ago
Quality Assurance Manager Open Book Extracts Roxboro, NC 27573
12 days ago
Technician, Quality Control (QC) Kolab Project Carleton Place, ON, Canada
11 days ago
Quality Assurance Project Coordinator Tilray Nanaimo, BC (+1 other)
3 days ago
Quality Assurance Manager Tilray, Inc. Bridgeport, IL
13 days ago
Quality Assurance Associate Cannimed By Aurora Canada
11 days ago
Quality Assurance Associate (Nights) Cannabis At Work Pickering, ON
5 days ago

Quality Manager

Elixinol Broomfield, CO 80021
Apply Now Copy link

Quality Manager

About Elixinol

Elixinol is a Colorado based CBD company seeking the best and the brightest employees in the industry. With deep roots in the hemp industry, Elixinol has been manufacturing and providing the highest-quality CBD hemp extracts in the world since its inception in 2014. We are currently growing and seeking high quality and highly motivated individuals to join our Operations corporate team.

Job Summary

The Quality Manager, reporting directly to the Director of Operations, will be responsible for managing and overseeing all quality assurance and quality control functions, supervising the quality assurance technicians, and working alongside the Operations team, among other responsibilities. The Quality Manager will be responsible for developing, implementing, and maintaining safety by directing the testing and quality assurance of Elixinol’s products and processes.

Responsibilities

  • Recruit and train quality technicians.
  • Work with other department managers in the Colorado facility for day-to-day facility operations and provide Quality related support to other departments.
  • Manage facility related Audit Program and maintain Audit Schedule and Completion Log.
  • Propose standard operation procedures where needed, train to and implement SOPs, as well as complete verification of effectiveness reviews at predetermined intervals.
  • Responsible for certification applications, renewal, compliance and reporting, scheduling/hosting audit of GMP and SQF, and fulfillment of any resulting corrective actions.
  • Manage scheduling, review, and updating of Quality records and manage Product Quality Plan and environmental monitoring program.
  • Manage and maintain critical state product and sales registrations.
  • Manage and direct internal HACCP and workers safety plans/committees.
  • Manage internal audit program and prepare appropriate reports and discuss with related personnel. As well as initiate, follow up, document, review, and file corrective action reports/deviation reports and implement corrective actions when procedures are not followed.
  • Assist Director of Operations to ensure compliance with customers' requirements as they pertain to the facility and oversee and review client, customer, and user feedback.
  • Assist Customer Service in management and evaluation of customer complaints with regards to product quality. Active input into CRM software required.
  • Oversee performance of QA to perform own reviews on documents including MMRs (Master Manufacturing Records), BPRs (Batch Production Records), and COAs (Certificates of Analysis).
  • Oversee the incoming inspection and release of all primary product components, labels and retail packaging for production use.
  • QA Manager has the authority on distribution of the product for OOS results that impact the quality and composition of ingredients or products.
  • Determine Quality check frequency and perform quality checks on the packaging lines to ensure that final products meet quality expectations and specifications.
  • Assist Validation Program by overseeing QA technologist and/or sampling personnel to make sure samples are pulled properly and pass to QC for testing.
  • Fill out appropriate portions of QAR forms to document material disposition decisions for any OOS results and file appropriate material disposal forms for rejected products.
  • Oversee Quality Assurance for production process control and make product disposition decisions and document any deviations in finished products.
  • Oversee QA to issue and maintain case specific corrective action reports for Corrective Action Program that violate suppliers/processing facilities/labs and distribute deviation reports to related departments/personnel. Assist Director of Operations with maintenance of Approved Supplier List, management of vendor surveys and scheduling of on-site audits, as necessary.

Qualifications

  • B.S. or B.A degree in business, engineering, or related field to the products being developed
  • Minimum 7 years' experience in a similar role
  • 3+ years of management experience in a supervisory role with direct reports
  • HACCP certified, SQF certified, and PCQI certified preferred

Work Conditions

Standard office: Sitting, typing, speaking, answering phones, communicating with others, standing, bending, walking, and occasional driving required. Must be able to lift up to 25 pounds at a time.

Work Hours: Normal business hours, occasional overtime required.

Job Type: Full-time

Salary: $67,000-$85,000/year

Education

  • Bachelor's (Required)

Work authorization

  • United States (Required)

Benefits

Excellent benefits package, eligible upon hire, including 10 paid holidays, 3 weeks of PTO, sick time, health insurance, company-paid life insurance, 401(k) match after 6 months of employment, product discounts - excellent overall benefits package.

This document describes the general nature and level of work performed by personnel assigned to this job classification. This document is not, however, an exhaustive list of all responsibilities, duties, and skills required of personnel so assigned. Elixinol reserves the right to add, revise, or delete job duties at any time.

Elixinol is both an Equal Opportunity, and At Will employer. The company does not discriminate on the basis of race, age, sex, religion, marital status, or sexual orientation. Either Company or Employee can terminate the employment relationship at any time for any legally permissible reason. Reasonable accommodations will be made for qualified candidates/employees with disabilities.

Job Type: Full-time

Pay: $67,000.00 - $85,000.00 per year

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Employee assistance program
  • Employee discount
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Parental leave
  • Professional development assistance
  • Vision insurance

Schedule:

  • 8 hour shift
  • Monday to Friday

COVID-19 considerations:
We require all staff and guests to wear masks at all times unless seated in office alone, social distancing, temperature checks upon entering building, routine cleanings, sanitization stations. We ensure our facility is a safe working environment.

Education:

  • Bachelor's (Preferred)

Experience:

  • management: 3 years (Preferred)
  • similar role: 7 years (Preferred)

License/Certification:

  • HACCP certified, SQF certified, and PCQI certified (Preferred)

Work Location:

  • One location

Work Remotely:

  • No
[{"employmentType":"","postedOn":"12 hours ago","description":"<div><p><b>Quality Manager</b></p><p><b>About Elixinol</b></p><p>Elixinol is a Colorado based CBD company seeking the best and the brightest employees in the industry. With deep roots in the hemp industry, Elixinol has been manufacturing and providing the highest-quality CBD hemp extracts in the world since its inception in 2014. We are currently growing and seeking high quality and highly motivated individuals to join our Operations corporate team.</p><p><b>Job Summary</b></p><p>The Quality Manager, reporting directly to the Director of Operations, will be responsible for managing and overseeing all quality assurance and quality control functions, supervising the quality assurance technicians, and working alongside the Operations team, among other responsibilities. The Quality Manager will be responsible for developing, implementing, and maintaining safety by directing the testing and quality assurance of Elixinol’s products and processes.</p><p><b>Responsibilities</b></p><ul><li>Recruit and train quality technicians.</li><li>Work with other department managers in the Colorado facility for day-to-day facility operations and provide Quality related support to other departments.</li><li>Manage facility related Audit Program and maintain Audit Schedule and Completion Log.</li><li>Propose standard operation procedures where needed, train to and implement SOPs, as well as complete verification of effectiveness reviews at predetermined intervals.</li><li>Responsible for certification applications, renewal, compliance and reporting, scheduling/hosting audit of GMP and SQF, and fulfillment of any resulting corrective actions.</li><li>Manage scheduling, review, and updating of Quality records and manage Product Quality Plan and environmental monitoring program.</li><li>Manage and maintain critical state product and sales registrations.</li><li>Manage and direct internal HACCP and workers safety plans/committees.</li><li>Manage internal audit program and prepare appropriate reports and discuss with related personnel. As well as initiate, follow up, document, review, and file corrective action reports/deviation reports and implement corrective actions when procedures are not followed.</li><li>Assist Director of Operations to ensure compliance with customers' requirements as they pertain to the facility and oversee and review client, customer, and user feedback.</li><li>Assist Customer Service in management and evaluation of customer complaints with regards to product quality. Active input into CRM software required.</li><li>Oversee performance of QA to perform own reviews on documents including MMRs (Master Manufacturing Records), BPRs (Batch Production Records), and COAs (Certificates of Analysis).</li><li>Oversee the incoming inspection and release of all primary product components, labels and retail packaging for production use.</li><li>QA Manager has the authority on distribution of the product for OOS results that impact the quality and composition of ingredients or products.</li><li>Determine Quality check frequency and perform quality checks on the packaging lines to ensure that final products meet quality expectations and specifications.</li><li>Assist Validation Program by overseeing QA technologist and/or sampling personnel to make sure samples are pulled properly and pass to QC for testing.</li><li>Fill out appropriate portions of QAR forms to document material disposition decisions for any OOS results and file appropriate material disposal forms for rejected products.</li><li>Oversee Quality Assurance for production process control and make product disposition decisions and document any deviations in finished products.</li><li>Oversee QA to issue and maintain case specific corrective action reports for Corrective Action Program that violate suppliers/processing facilities/labs and distribute deviation reports to related departments/personnel. Assist Director of Operations with maintenance of Approved Supplier List, management of vendor surveys and scheduling of on-site audits, as necessary.</li></ul><p><b>Qualifications</b></p><ul><li>B.S. or B.A degree in business, engineering, or related field to the products being developed</li><li>Minimum 7 years' experience in a similar role</li><li>3+ years of management experience in a supervisory role with direct reports</li><li>HACCP certified, SQF certified, and PCQI certified preferred</li></ul><p><b>Work Conditions</b></p><p>Standard office: Sitting, typing, speaking, answering phones, communicating with others, standing, bending, walking, and occasional driving required. Must be able to lift up to 25 pounds at a time.</p><p><b>Work Hours: </b> Normal business hours, occasional overtime required.</p><p><b>Job Type: </b> Full-time</p><p><b>Salary: </b> $67,000-$85,000/year</p><p><b>Education</b></p><ul><li>Bachelor's (Required)</li></ul><p><b>Work authorization</b></p><ul><li>United States (Required)</li></ul><p><b>Benefits</b></p><p>Excellent benefits package, eligible upon hire, including 10 paid holidays, 3 weeks of PTO, sick time, health insurance, company-paid life insurance, 401(k) match after 6 months of employment, product discounts - excellent overall benefits package.</p><p><i>This document describes the general nature and level of work performed by personnel assigned to this job classification. This document is not, however, an exhaustive list of all responsibilities, duties, and skills required of personnel so assigned. Elixinol reserves the right to add, revise, or delete job duties at any time.</i></p><p><i>Elixinol is both an Equal Opportunity, and At Will employer. The company does not discriminate on the basis of race, age, sex, religion, marital status, or sexual orientation. Either Company or Employee can terminate the employment relationship at any time for any legally permissible reason. Reasonable accommodations will be made for qualified candidates/employees with disabilities.</i></p><p>Job Type: Full-time</p><p>Pay: $67,000.00 - $85,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Employee assistance program</li><li>Employee discount</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Parental leave</li><li>Professional development assistance</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>COVID-19 considerations:<br />We require all staff and guests to wear masks at all times unless seated in office alone, social distancing, temperature checks upon entering building, routine cleanings, sanitization stations. We ensure our facility is a safe working environment.</p><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>management: 3 years (Preferred)</li><li>similar role: 7 years (Preferred)</li></ul><p>License/Certification:</p><ul><li>HACCP certified, SQF certified, and PCQI certified (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Public/Established","name":"Elixinol","logoUrl":"/logos/elixinol-2c3cedd7761e2a33a7bed7f207151b6c.png"},"location":{"country":"United States","address":"Broomfield, CO 80021","city":"Broomfield","stateProvince":"CO"},"frontendLink":"/job-posting/elixinol/quality-manager/2751f862bfdcc0e408885bce9e99b157","title":"Quality Manager","hash":"2751f862bfdcc0e408885bce9e99b157","postingUrl":"https://www.indeed.com/job/quality-manager-c39a6112320493b5"},{"postedOn":"5 days ago","description":"<div><div><h2><b>COMPANY OVERVIEW</b></h2><p>Recently named one of <i>Entrepreneur</i> magazine's 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, Cresco's 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 Mindy's, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco's 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 industry's 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><h2><b>MISSION STATEMENT</b></h2><p>At Cresco, we aim to lead the nation's 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 Manager to join our Fall River Facility. As the Quality Manager, you will be responsible for overseeing quality-related activities at the facility associated with incoming inspection, sampling and inspection of finished products, customer complaint investigations, product investigations, and Corrective and Preventive Action (CAPA) plans.</p><p>Product families may include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges, transdermal patches), and food products (chocolate, gummies, cookies). This position will be responsible for ensuring products are being produced in a manner that meets all specifications and follows brand consistency. You will also lead efforts to identify potential quality risks and work with operations personnel to develop improvement opportunities.</p><p><b>CORE JOB DUTIES</b></p><ul><li>Responsible for management of site Quality Assurance staff</li><li>Performs finished product sampling and inspection</li><li>Performs equipment and product line clearances before production runs</li><li>Manages and writes customer complaints and product investigations, helping to assess risk, identify root cause, CAPA plans, and implementing solutions with business partners</li><li>Assist with QMS document writing and revisions, including routing and/or approval of change request packages</li><li>Inspects packaged orders to ensure correct content and quantities, as deemed necessary</li><li>Inspects retain samples and customer return samples, as deemed necessary</li><li>Reviews in-process batch documentation, logbooks, test results, and good documentation practices</li><li>Discusses issues and concerns directly with line personnel and operations management so any corrections and improvements can be made in a timely manner</li><li>Performs reviews and audits as assigned</li><li>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</li><li>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</li><li>Monitors compliance to established Good Manufacturing Practice (GMP) and SQF (Safe Quality Foods) guidance</li><li>Facilitates creation of and/or updates to product safety plans or product process parameters</li><li>Provides recommendations for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management</li><li>Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines</li><li>5-10% travel to other facilities and states to help with new market launches, training, etc.</li></ul><p><b>REQUIRED EXPERIENCE, EDUCATION AND SKILLS</b></p><ul><li>Bachelors Degree and 5+ years' experience in a quality role</li><li>Prior experience in a highly regulated industry required (i.e.: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis)</li><li>Prior experience managing and mentoring large teams, required</li><li>FDA, HACCP, and/or SQF experience, preferred</li><li>Prior experience in Quality Assurance or Quality Control function</li><li>Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA</li><li>Prior experience with regulatory agency audits and correspondence</li><li>Ability to follow written procedures and monitor others for adherence to written procedures</li><li>Ability to create or update written procedures with site operations personnel</li><li>Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies</li><li>Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</li></ul><p><b>ADDITIONAL REQUIREMENTS</b></p><ul><li>Must be 21 years of age or older to apply</li><li>Must comply with all legal or company regulations for working in the industry</li></ul><p><i>Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.</i></p></div></div>","company":{"companyType":"Public/Established","name":"Cresco Labs","logoUrl":"/logos/cresco-labs-af2becc596b572034007bd7a7d918bdd.png"},"location":{"country":"United States","address":"Fall River, MA","city":"Fall River","stateProvince":"MA"},"frontendLink":"/job-posting/cresco-labs/quality-manager/dfe327a6164f04fdbdbbc07da8e442f7","title":"Quality Manager","hash":"dfe327a6164f04fdbdbbc07da8e442f7","postingUrl":"https://www.indeed.com/job/quality-manager-a1e9d0d5b7473cd7"},{"employmentType":"Full-time","postedOn":"13 hours ago","description":"<div><p>An accredited top cannabis testing lab in Los Angeles is looking for a Quality Manager to join their team!</p><p><b>Job Summary: </b></p><p>The Quality Manager is responsible for the implementation of the lab’s quality program and ensuring all laboratory activities are in compliance with BCC regulations and ISO/IEC 17025 standards.</p><p><b>Job Duties: </b></p><p>· Lead the team with dynamic leadership that promotes an environment of support, development, engagement, and high productivity. This includes, but is not limited to, hiring, coaching, performance management, ensuring productivity, disciplinary action, cross-training, rewards and recognition, and succession planning.</p><p>· Ensure quality assurance/control compliance and standardization. This requires maintaining current knowledge of internal and external standards, with particular focus on BCC and ISO/IEC 17025.</p><p>· Create, manage, and facilitate the quality scorecard.</p><p>· Effectively communicate quality policies and procedures to all levels of laboratory staff.</p><p>· Establish and maintain documentation and record controls and procedures.</p><p>· Develop and implement quality procedures and standards to ensure production activities meet compliance standards.</p><p>· Create and update laboratory policies and procedures associated with various assays, in partnership with the Lab Director and Quality department.</p><p>· Monitor laboratory data performance and customer complaints with tracking and establish corrective measures as needed. Prepare detailed reports, including current, trending, forecasting.</p><p>· Manage internal and external audits. Investigate findings, work with the affected department(s) to develop appropriate corrective and/or preventive actions, document the findings, and perform appropriate follow-up. Evaluate the efficacy of implemented corrective/preventive methods.</p><p>· Generate audit reports and schedule review with appropriate internal stakeholders.</p><p>· Manage the proficiency testing (PT) program for the laboratory. This includes PT vendor evaluation, purchasing PT samples, scheduling PT tests, and reviewing submissions.</p><p>· Monitor relevant data for performance and trends using statistical methods.</p><p>· Build strong internal, external, and cross-functional relationships.</p><p>· Other duties and special projects as assigned.</p><p><b>Requirements: </b></p><p>· Ability to maintain an incredibly high degree of attention to detail and accuracy.</p><p>· Ability to maintain confidence, confidentially, and composure during difficult and/or complex situations.</p><p>· Ability to work in a dynamic, fast-paced deadline environment while successfully managing multiple tasks.</p><p>· Strong knowledge of Microsoft Office, including Excel, PowerPoint, and Word.</p><p>· Strong understanding of standard laboratory protocol.</p><p>· Excellent communication skills and ability to effectively work, influence, problem solve, and communicate with all levels of the organization.</p><p>· Proven track record in people leadership (supporting, developing, engaging) with demonstrated teambuilding and collaboration skills.</p><p>· Proven track record in adapting to change and accelerating the performance of laboratory groups.</p><p>· Demonstrated ability to be well balanced between the strategic view of the work and the execution aspect of the role.</p><p>· Required: A bachelor’s degree in a scientific discipline from a four-year college or university plus at least seven (7) years of relevant regulated industry experience (BCC, ISO, FDA, EPA, USP, etc.).</p><p>· Required: Knowledge of principles, terminology, practices, techniques, and instrumentation commonly used in a laboratory setting.</p><p>· Preferred: Supervisory/management experience.</p><p>· Preferred: Exposure to the cannabis industry.</p><p><b>Benefits Include: </b></p><p>Health, dental, and vision insurance, 401k, paid time off, and floating holidays.</p><p><i>Cannabis Consulting Group provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</i></p><p><i>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.</i></p><p>Job Type: Full-time</p><p>Pay: Up to $90,000.00 per year</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Cannabis Consulting Group","logoUrl":"/logos/canna-resource-group-00d8790a186447a65a99dc4b54db7f84.jpeg"},"location":{"country":"United States","address":"Los Angeles, CA 91406","city":"Los Angeles","stateProvince":"CA"},"frontendLink":"/job-posting/cannabis-consulting-group/cannabis-quality-manager/2c4cec38849f54cdd817ff9281820468","title":"Cannabis Quality Manager","hash":"2c4cec38849f54cdd817ff9281820468","postingUrl":"https://www.indeed.com/job/cannabis-quality-manager-21ae749e488d02a7"},{"employmentType":"Full-time","postedOn":"20 days ago","description":"<div><p>COMPANY OVERVIEW Recently named one of Entrepreneur magazine's Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States.</p><p>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.</p><p>Employing a consumer-packaged goods (\"CPG\") approach to cannabis, Cresco's 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 Mindy's, a line of edibles created by James Beard Award-winning chef Mindy Segal.</p><p>Sunnyside, Cresco's national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers.</p><p>Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry's 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>MISSION STATEMENT At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction.</p><p>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.</p><p>As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.</p><p>JOB SUMMARY Cresco Labs is seeking a Quality Assurance (QA) Specialist to join our manufacturing facility.</p><p>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).</p><p>This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency.</p><p>You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities.</p><p>The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.</p><p>CORE JOB DUTIES 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 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.</p><p>Provides advice with process improvements to eliminate errors and reduce risk.</p><p>Monitors compliance to established Good Manufacturing Practice (GMP) guidance.</p><p>Executes action plans for product quarantine, destruction, rework, withdrawal/recall Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>REQUIRED EXPERIENCE, EDUCATION AND SKILLS Bachelor's degree, 3-5 years' experience or Associate Degree, 5+ years' experience Prior experience in highly regulated industry.</p><p><b>Highly desirable:</b></p><p>healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis.</p><p>FDA, HACCP, SQF experience Prior experience in Quality Assurance or Quality Control function Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA Ability to follow written procedures and monitor others for adherence to written procedures Ability to create or update written procedures with site operations personnel Strong written and verbal communication skills Detail-oriented Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions ADDITIONAL REQUIREMENTS Must be 21 years of age or older to apply Must comply with all legal or company regulations for working in the industry Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status</p></div>","company":{"website":"crescolabs.com","companyType":"Public/Established","name":"Cresco Labs","_id":"603174527d3eb30012cc2a2d","logoUrl":"/logos/cresco-labs-af2becc596b572034007bd7a7d918bdd.png"},"location":{"country":"United States","address":"Mendota, CA","city":"Mendota","stateProvince":"CA"},"frontendLink":"/job-posting/cresco-labs/quality-control-quality-assurance-specialist/57318677a88a06e185995765ba967fbf","title":"Quality Control / Quality Assurance Specialist","hash":"57318677a88a06e185995765ba967fbf","postingUrl":"https://www.jobilize.com/amp/job/quality-control-assurance-specialist-mendota-cresco-labs-united-states"},{"employmentType":"Full-time","postedOn":"7 days ago","description":"<div><p>Trovaro is a cannabis-focused staffing &amp; recruiting firm working with a variety of clients across the U.S. and Canada. This role is with a powerhouse client based in Chicago, IL with offices located across the U.S.</p><p>Cannabis experience required</p><p><b>About the Role:</b></p><p>We're seeking a Product Quality Assurance Manager to join our team.</p><p>You will be responsible for overseeing innovation quality specific to Flowers &amp; Extracts across the enterprise. Associated quality activities involve serving as process owner, subject matter expert, and Gatekeeper for the category through out the stage-gate process. This position will be responsible for ensuring products are being designed and launched in a manner that meets all specifications and brand consistency. You will also lead efforts to track and trend product issues post launch and identify potential quality risks while working with operations and R&amp;D personnel to develop improvement opportunities. The ideal candidate must demonstrate strong leadership, be a strong communicator, have a breadth of quality experience, and ability to work within a highly regulated industry.</p><p><b>Core Duties:</b></p><p>• Assists in the development of brand and product quality standards for all product categories: flower and flower products; oils, extracts and medicinal; infused edibles and beverages</p><p>• Leading product quality expert throughout the product innovation process and product commercialization including monitoring, investigations and technical CAPA in relations to quality and safety complaints of new products</p><p>• Leads the quality aspect of new products’ line extensions to various sites</p><p>• Ensures facilities launching new products are fully equipped with all quality documentation and quality personnel are properly trained to guarantee a successful integration.</p><p>• Manages new product trial assessments from a quality perspective and an active approver of all new products prior to launch.</p><p>• Subject matter expert for site quality personnel in relations to new products and launches.</p><p>• Assesses all new equipment and manufacturing processes for products safety and quality risks to ensure equipment is suitable for the intended process and products</p><p>• Serves as an escalation point for product quality issues that span across multiple sites, products, etc.</p><p>• Provides technical support to the Quality Systems Director in the development of Food Safety and Product Quality Plans for new products – responsible for the ingredient and process risk assessments</p><p>• Leads the development and maintenance of Product Quality Specifications for all product categories – partners with R&amp;D managers to develop technical product parameters and ensure adherence to specified limits</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• 25-30% to facilities and states as the need arises</p><p><b>Required Skills &amp; Education:</b></p><p>• Bachelor’s degree (in Food Science, Biology, Chemistry preferred), 5+ years’ experience in a quality role.</p><p>• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA/FSMA, HACCP, GFSI experience i.e. SQF, BRC, etc.</p><p>• Prior experience with manufacturing quality, stability programs, product development, sampling and testing, packaging and labeling, batch record reviews, product inspections, batch/lot release, material quarantine, product withdrawals/recalls.</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>• Detail-oriented</p><p>• Ability to work autonomously and timely in a fast pace growing environment</p><p>• Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</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":{"companyType":"Private/Startup","name":"Trovaro","logoUrl":"/logos/trovaro-880b6e5aae3e26c4d6293c45d7ccb8f7.png"},"location":{"country":"United States","address":"Chicago, IL, USA (+1 other)","city":"Chicago","stateProvince":"IL"},"frontendLink":"/job-posting/trovaro/cannabis-product-quality-manager/e742634fa71da9b28b4e1e02d1a63278","title":"Cannabis Product Quality Manager","hash":"e742634fa71da9b28b4e1e02d1a63278","postingUrl":"https://www.recruit.net/job/product-quality-manager-jobs/9EFC4443E7C1EBDA"},{"employmentType":"Full-time","postedOn":"10 days ago","description":"<div><p>Trovaro is a cannabis-focused staffing &amp; recruiting firm working with a variety of clients across the U.S. and Canada. This role is with a powerhouse client based in Chicago, IL with offices located across the U.S.</p><p><b>About the Role:</b></p><p>We're seeking a Product Quality Assurance Manager (Flower &amp; Extracts) to join the Chicago headquarters. You will be responsible for overseeing innovation quality specific to Flowers &amp; Extracts across the enterprise. Associated quality activities involve serving as process owner, subject matter expert, and Gatekeeper for the category through out the stage-gate process. This position will be responsible for ensuring products are being designed and launched in a manner that meets all specifications and brand consistency. You will also lead efforts to track and trend product issues post launch and identify potential quality risks while working with operations and R&amp;D personnel to develop improvement opportunities. The ideal candidate must demonstrate strong leadership, be a strong communicator, have a breadth of quality experience, and ability to work within a highly regulated industry.</p><p><b>Core Duties:</b></p><p>• Assists in the development of brand and product quality standards for all product categories: flower and flower products; oils, extracts and medicinal; infused edibles and beverages</p><p>• Leading product quality expert throughout the product innovation process and product commercialization including monitoring, investigations and technical CAPA in relations to quality and safety complaints of new products</p><p>• Leads the quality aspect of new products’ line extensions to various sites</p><p>• Ensures facilities launching new products are fully equipped with all quality documentation and quality personnel are properly trained to guarantee a successful integration.</p><p>• Manages new product trial assessments from a quality perspective and an active approver of all new products prior to launch.</p><p>• Subject matter expert for site quality personnel in relations to new products and launches.</p><p>• Assesses all new equipment and manufacturing processes for products safety and quality risks to ensure equipment is suitable for the intended process and products</p><p>• Serves as an escalation point for product quality issues that span across multiple sites, products, etc.</p><p>• Provides technical support to the Quality Systems Director in the development of Food Safety and Product Quality Plans for new products – responsible for the ingredient and process risk assessments</p><p>• Leads the development and maintenance of Product Quality Specifications for all product categories – partners with R&amp;D managers to develop technical product parameters and ensure adherence to specified limits</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• 25-30% to facilities and states as the need arises</p><p><b>Required Skills &amp; Education:</b></p><p>• Bachelor’s degree (in Food Science, Biology, Chemistry preferred), 5+ years’ experience in a quality role.</p><p>• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA/FSMA, HACCP, GFSI experience i.e. SQF, BRC, etc.</p><p>• Prior experience with manufacturing quality, stability programs, product development, sampling and testing, packaging and labeling, batch record reviews, product inspections, batch/lot release, material quarantine, product withdrawals/recalls.</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>• Detail-oriented</p><p>• Ability to work autonomously and timely in a fast pace growing environment</p><p>• Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</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":{"companyType":"Private/Startup","name":"Trovaro","logoUrl":"/logos/trovaro-880b6e5aae3e26c4d6293c45d7ccb8f7.png"},"location":{"country":"United States","address":"Berwyn Heights, MD","city":"Berwyn Heights","stateProvince":"MD"},"frontendLink":"/job-posting/trovaro/cannabis-product-quality-manager/e7e1a0aa1ca3db9ddf30ed063d970798","title":"Cannabis Product Quality Manager","hash":"e7e1a0aa1ca3db9ddf30ed063d970798","postingUrl":"https://www.jobilize.com/amp/job/cannabis-product-quality-manager-berwyn-heights-trovaro-united-states"},{"employmentType":"Full-time","postedOn":"19 days ago","description":"<div><p>Trovaro is a cannabis-focused staffing &amp; recruiting firm working with a variety of clients across the U.S. and Canada. This role is with a powerhouse client based in Chicago, IL with offices located across the U.S.</p><p><b>About the Role:</b></p><p>We're seeking a Product Quality Assurance Manager (Flower &amp; Extracts) to join the Chicago headquarters. You will be responsible for overseeing innovation quality specific to Flowers &amp; Extracts across the enterprise. Associated quality activities involve serving as process owner, subject matter expert, and Gatekeeper for the category through out the stage-gate process. This position will be responsible for ensuring products are being designed and launched in a manner that meets all specifications and brand consistency. You will also lead efforts to track and trend product issues post launch and identify potential quality risks while working with operations and R&amp;D personnel to develop improvement opportunities. The ideal candidate must demonstrate strong leadership, be a strong communicator, have a breadth of quality experience, and ability to work within a highly regulated industry.</p><p><b>Core Duties:</b></p><p>• Assists in the development of brand and product quality standards for all product categories: flower and flower products; oils, extracts and medicinal; infused edibles and beverages</p><p>• Leading product quality expert throughout the product innovation process and product commercialization including monitoring, investigations and technical CAPA in relations to quality and safety complaints of new products</p><p>• Leads the quality aspect of new products’ line extensions to various sites</p><p>• Ensures facilities launching new products are fully equipped with all quality documentation and quality personnel are properly trained to guarantee a successful integration.</p><p>• Manages new product trial assessments from a quality perspective and an active approver of all new products prior to launch.</p><p>• Subject matter expert for site quality personnel in relations to new products and launches.</p><p>• Assesses all new equipment and manufacturing processes for products safety and quality risks to ensure equipment is suitable for the intended process and products</p><p>• Serves as an escalation point for product quality issues that span across multiple sites, products, etc.</p><p>• Provides technical support to the Quality Systems Director in the development of Food Safety and Product Quality Plans for new products – responsible for the ingredient and process risk assessments</p><p>• Leads the development and maintenance of Product Quality Specifications for all product categories – partners with R&amp;D managers to develop technical product parameters and ensure adherence to specified limits</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• 25-30% to facilities and states as the need arises</p><p><b>Required Skills &amp; Education:</b></p><p>• Bachelor’s degree (in Food Science, Biology, Chemistry preferred), 5+ years’ experience in a quality role.</p><p>• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA/FSMA, HACCP, GFSI experience i.e. SQF, BRC, etc.</p><p>• Prior experience with manufacturing quality, stability programs, product development, sampling and testing, packaging and labeling, batch record reviews, product inspections, batch/lot release, material quarantine, product withdrawals/recalls.</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>• Detail-oriented</p><p>• Ability to work autonomously and timely in a fast pace growing environment</p><p>• Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</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":{"companyType":"Private/Startup","name":"Trovaro","logoUrl":"/logos/trovaro-880b6e5aae3e26c4d6293c45d7ccb8f7.png"},"location":{"country":"United States","address":"Chicago, IL (+1 other)","city":"Chicago","stateProvince":"IL"},"frontendLink":"/job-posting/trovaro/jooble-cannabis-product-quality-manager/cf28d7d091bf8bc73abc8269b92d9388","title":"Jooble - Cannabis Product Quality Manager","hash":"cf28d7d091bf8bc73abc8269b92d9388","postingUrl":"https://jooble.org/jdp/-4780603731524651147/Cannabis-Product-Quality-Manager-Chicago%2C-IL"},{"postedOn":"12 hours ago","description":"<div><div><p><b>About </b><b>Charlotte's Web:</b></p><p>Charlotte's Web products are made from our world-renowned hemp genetics grown 100% in the USA.<br />Founded by the Stanley Brothers of Colorado, Charlottes Web leads the industry in quality, safety, consistency and social responsibility to improve thousands of lives daily through the use of Charlotte's Web.<br />At Charlottes Web, we are driven by principles that extend far beyond the bottom line. It is our goal to provide products of the highest possible quality, while contributing to the sustainability of the communities we have the privilege of serving.</p><p></p><p><b>Position Summary:</b></p><p>The primary responsibility of this position is to execute against the procedures for the manufacture, storage, and distribution of dietary supplements. This position requires utilization of the Code of Federal Regulations (21 CFR Part 111), including but not limited to control of raw materials, components, intermediates and final products.</p><p><b><br />Essential Duties and Responsibilities:</b></p><ul><li>Own and perform raw material quality disposition</li><li>Provide a broad range of quality oversight for the warehouse and raw materials program</li><li>Perform compliance review on the following records: batch record (includes on-the-floor review of records); release data</li><li>Determine raw material disposition</li><li>Initiate and own Deviations, CAPAs, and change controls as appropriate</li><li>Work directly with manufacturing, the laboratory and other departments responsible for GMP activities to resolve deviations and other compliance issues in a timely manner</li><li>Perform warehouse walk-through on a regular basis to maintain area in cGMP compliance state</li><li>Support internal audits of departments involved in GMP activities</li><li>Assist in other Quality Assurance activities as needed, i.e. Batch Record Review, Equipment Log Review</li><li>Support client and regulatory audits</li><li>React to change productivity and handle other essential tasks</li></ul><p></p><p><b>Qualifications:</b></p><ul><li>Bachelors Degree in Engineering (Biomedical, Mechanical, Chemical, or Electrical) or Science (Biology) preferred</li><li>1-2 years experience in a Quality Assurance role for medical device, food, dietary supplement or pharmaceutical manufacturing</li><li>Experience handling Co-Manufacturer compliance required</li><li>Demonstrates excellent organizational and communication skills and proficiency with the MS Office Suite, and statistical software</li><li>Must be able to work independently with minimal supervision</li><li>Able to prioritize projects and manage Quality Assurance resources to meet organizational goals and objectives</li></ul><p></p><p><b>Compensation:</b></p><p>$18.55 - $27.85</p><p></p><p>Charlottes Web provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</p><p>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Charlottes Web is an At-Will Employer.</p><p>V1.0</p></div></div>","company":{"companyType":"Public/Established","name":"Charlottes Web","logoUrl":"/logos/charlottes-web-hemp-902e2edc0fd77f5d49ab925ac37fc7b6.png"},"location":{"country":"United States","address":"Louisville, CO 80027","city":"Louisville","stateProvince":"CO"},"frontendLink":"/job-posting/charlottes-web/quality-assurance-associate/361470cf76b212ade7d2f47330d60c19","title":"Quality Assurance Associate","hash":"361470cf76b212ade7d2f47330d60c19","postingUrl":"https://www.indeed.com/job/quality-assurance-associate-2f351a5cd3d1a645"},{"employmentType":"Full-time","postedOn":"2 days ago","description":"<div><p>Adecco is currently looking to hire a Quality Assurance Associate for our cannabis client in Grimsby, ON. This is for an immediate start for minimum one month for $19.00/hour. The role will also be responsible for ensuring compliance with various regulations and as itpertains to the Cannabis industry as well as Good Production and ManufacturingPractices (GPP/GMP).ESSENTIAL FUNCTIONS ? Ensure that all standard operating procedures are being strictly followed at alltimes? Ensure compliance with Cannabis Regulations (CR)? Help implement and maintain GPP? Collaborate with other departments to ensure compliance with standardoperating procedures? Perform internal QA audits that are compliant with corporate policies, practices,and procedures? Adopt and incorporate quality methods into everyday work? Identify relevant QA training needs and opportunities? Conduct tests and create reports in compliance with corporate policies, practices,and procedures? Assist with the maintenance of QA monitoring programs, including audits,controls, and other qualifiers? Conduct risk analysis, verification, validation activities, and formal designreviews, as applicable? Support processes of suppliers and service providers? Ensure that refuse and cannabis products are managed or destroyed inaccordance with Cannabis Regulations (CR)? Complete inspection reports on production equipment, sanitation practices, andproduction areas? Train staff on operating procedures and GPP? Recommend corrective action? Adhere to all occupational health and safety regulations? Other duties as assignedROLE REQUIREMENTS/ABILITIES Experience / Education ? At least three years of work experience in a quality assurance role inpharmaceutical, food, or related industry? Postsecondary degree or diploma in biological science (chemistry, biology,pharmacology)? Cannabis or greenhouse industry experience would be considered an assetSkills &amp; Abilities? Knowledge of The Cannabis Act and its supporting regulations are an asset? Experience with an organization regulated by HACCP Canada or experience in asimilarly regulated environment (GMP, GAP, GPP)? Ability to follow strict operating procedures? Ability to work individually as well as part of a team? Ability to adapt to new technology? Dedication to safety measures and best practices? Ability to prioritize and manage conflicting demands? Ability to effectively communicate both verbally and in writing? High level of integrity and work ethic? Must have own transportation as we are not on a public transportation routeWorking Conditions ? Constant exposure to the smell of cannabis? Manual dexterity required to use desktop computer? Working in a busy environment with frequent interruptions? Use of required personal protective equipmentAccommodation will be provided in all parts of the hiring process as required under Adecco’s Employment Accommodation policy. Applicants will need to make their needs known in advance to their Adecco representative.I am authorized to work in Canada for any employer.* Yes No Upload or attach document from Your device Dropbox Google Drive Or Enter you work experience including both job title and job duties. Attaching your resume provides our consultants a better understanding of your work history and helps improve placement opportunities. Job Title Warehouse manager Job Duties Write about the work you’ve done and any special skills you have. I agree to the Terms of use and Application agreement.* You must agree to the Terms of use and Application agreement to proceed. Adecco is looking to hire a Sanitation Associate for our cannabis client in Grimsby, ON. This role is for an immediate start for $16/hour. The Sanitation Associate will be responsible for keeping production buildings and office building in... Adecco is currently hiring a Warehouse Associates in Burlington . The pay rate for this role is $15.00+ per hour. Please apply below as soon as possible if you are interested. Responsibilities: Receive and inspect inbound product according to... General Labourer Interested in getting paid weekly? If so, it’s all possible with this General Labourer job in St. Catharines, ON. Adecco is currently hiring for a temporary, part-time to full time General Labourer to work a n ongoing</p></div>","company":{"website":"adecco.ca","companyType":"Public/Established","name":"Adecco Canada","logoUrl":"/logos/adecco-a6e8d4caff6004eecbacd479e51def08.png"},"location":{"country":"Canada","address":"Grimsby, ON","city":"Grimsby","stateProvince":"ON"},"frontendLink":"/job-posting/adecco-canada/quality-assurance-associate/4287c8663a1fa492b8869c05fd625eff","title":"Quality Assurance Associate","hash":"4287c8663a1fa492b8869c05fd625eff","postingUrl":"https://ca.trabajo.org/job-649-20210503-927ca4783ac8fe4a680516d3adba8c2a"},{"employmentType":"Full-time, Permanent","postedOn":"3 days ago","description":"<div><p><i>Quality Assurance </i><br />We are looking for a full time Quality Assurance Person that will be responsible for developing and maintaining compliance protocols for a private cannabis manufacturing company located in Vaughan. We are seeking a self-motivated, experienced, dedicated and passionate Quality Assurance and Document Control Specialist to join our team.</p><p>Reporting to the President, the Quality Assurance and Document Control Specialist will be responsible for assisting in the creation and implementation of SOP’s, quality operations; including, training, auditing, document control, record keeping, and ensuring compliance with all applicable regulations. This person will ensure consistent quality of edible cannabis production by enforcing appropriate Preventative Control Plans, in conjunction with establishing GPP and GMP systems.</p><p>If you are an advocate for the cannabis industry, interested in sustainable business practices and working in a small environment, then this may be the job for you!</p><p>Main Responsbilities</p><ul><li>Achieve Quality Assurance operational objectives by contributing information and analysis to strategic plans and reviews; identify and resolve problems; identify and implement system improvements, standards and drive positive change.</li></ul><ul><li>Development and maintaining of all required PCP’s (Preventative Control Plan) for edible cannabis product manufacturing.</li></ul><ul><li>Mentor other employees in implementing continuous product improvement initiatives for edible cannabis product manufacturing.</li></ul><ul><li>Execute QA plans by assisting in conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions and verification procedures.</li></ul><ul><li>Work closely with the President to ensure that all products are being developed in a manner compliant with all applicable regulations, policies and procedures.</li></ul><ul><li>Prepare quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions and re-validations.</li></ul><ul><li>Perform any other job duties as needed including but not limited to production, inventory maintenance, and general cleaning</li></ul><p>Skills and Requirements</p><ul><li>2 years of experience working in document control or creating effective SOPs in the Cannabis industry</li></ul><ul><li>Strong Computer Skills</li></ul><ul><li>Excellent written and verbal communication skills</li></ul><ul><li>Excellent organizational skills, attention to detail, and a positive attitude</li></ul><ul><li>Understanding of the application of laws, regulations, and policies for safe food manufacturing as it applies to cannabis edible product manufacturing.</li></ul><ul><li>Team player who thrives in a fast paced,small environment. Ability to anticipate and communicate potential risks and strategize creative, workable solutions.</li></ul><ul><li>Strategic thinker adept at working cross-functionally to achieve goals in a timely manner</li></ul><ul><li>Self-starter with a strong ability to multi-task to meet multiple deadlines and changing priorities.</li></ul><ul><li>Proficiency in MS Office, particularly Excel and experience using ERP systems.</li></ul><p>Job Types: Full-time, Permanent</p><p>Salary: From $50,000.00 per year</p><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Education:</p><ul><li>Bachelor's Degree (preferred)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 1 year (preferred)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Blossim Inc.","logoUrl":"/logos/blossim-inc-f0c2db8826dd1aaf1bfc3f176b42796f.png"},"location":{"country":"Canada","address":"Vaughan, ON","city":"Vaughan","stateProvince":"ON"},"frontendLink":"/job-posting/blossim-inc/quality-assurance-analyst/7d9f15b36c4a290afa87fddb0c76d020","title":"Quality Assurance Analyst","hash":"7d9f15b36c4a290afa87fddb0c76d020","postingUrl":"https://ca.indeed.com/job/quality-assurance-analyst-29e154cd3829f16d"},{"employmentType":"Full-time","postedOn":"4 days ago","description":"<div><p><b>Quality Assurance SupervisorDescriptionJob Title:</b></p><p><b>Quality Assurance SupervisorDepartment:</b></p><p><b>Quality Assurance- CultivationReports to:</b></p><p><b>Quality Assurance ManagerFLSA Status:</b></p><p><b>ExemptLocation:</b></p><p><b>Tallahassee, FLRole Summary:</b></p><p>The Quality Assurance Supervisor is responsible for overseeing productivity and personnel relations of the Quality Assurance Techs and Shift Leads.</p><p>Additionally, the QA-C Supervisor will work in concert with various department Managers and Supervisors, as needed, to ensure departmental directives and needs are met.</p><p>The QA-C Supervisor will be responsible for setting goals for performance and deadlines in ways that streamline productivity and limit bottlenecks in work-flow.</p><p>Furthermore, organizing work-flow and ensuring that employees understand their duties or delegated tasks will be of top priority.</p><p>Also, monitoring employee productivity and providing constructive feedback and coaching as needed.</p><p><b>The QA-C Supervisor reports directly to the QA-C Manager.Key Duties and ResponsibilitiesMonitoring Employee Productivity and Providing Constructive FeedbackSetting Individual and Team Goals, Daily &amp; Weekly, and Holding Team/Individuals AccountableOrganizing Work-Flow and working with Shift Lead to Create Peak OptimizationTime Management and Time Sheet ApprovalCoaching and Disciplinary Action and DocumentationAide with Staffing and DevelopmentAide with SOP DevelopmentApprove Designated Sorted Material as Bulk, \"Mini's\", and TrimCommunicate Data Entry Errors with Lead(s)Position RequirementsSKILLS AND QUALIFICATIONSManagement ExperienceLeadershipCommunicationConflict ResolutionTime ManagementInterpersonal SkillsCritical ThinkingFamiliarization with KPIsADDITIONAL REQUIRMENTS:</b></p><p><b>Must be able to pass a Level 2 background screeningMust be at least 21 years of age (State Law)Experience leading a small teamPHYSICAL REQUIREMENTS:</b></p><p>Must be able to push, pull, move, and/or lift a minimum of 40lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistanceMust be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stopping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasksMust be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater)Must have visual acuity with/without job aids to perform activities such as; reading, viewing a computer terminal, visual inspection involving small parts/details.</p><p>Clarity of vision at 20 ft or more in day and night/dark conditionsMust be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc.</p><p><b>(Moderate noise)WORK SCHEDULE:</b></p><p>40+ hours weekly with flexible hours depending on department needs.</p><p>Must be available to work occasional evenings, weekends, and holidaysEqual Opportunity Employer l Trulieve Supports a Drug Free WorkplaceFull-Time/Part-TimeFull-Time ShiftVarious Shifts Level 2 Background check requiredyes PositionQuality Assurance Supervisor DivisionTrulieve, INC Close DatePost Internal Days0 Number of Openings1 Number Filled0 Exempt/Non-ExemptExempt Req NumberCUL-21-00060 Open Date3/1/2021 LocationTallahassee EOE StatementWe are an equal employment opportunity employer.</p><p>All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.</p><p>This position is currently accepting applications</p></div>","company":{"website":"trulieve.com","companyType":"Public/Established","name":"Trulieve Cannabis","logoUrl":"/logos/trulieve-1d76a294c42e35e1fad949d6f74742d9.png"},"location":{"country":"United States","address":"Tallahassee, FL, USA","city":"Tallahassee","stateProvince":"FL"},"frontendLink":"/job-posting/trulieve-cannabis/quality-assurance-supervisor/d76ffe5eb638dafb3e518a262f23ee3a","title":"Quality Assurance Supervisor","hash":"d76ffe5eb638dafb3e518a262f23ee3a","postingUrl":"https://www.jobilize.com/amp/job/quality-assurance-supervisor-tallahassee-trulieve-cannabis-united-49173dab2936af"},{"postedOn":"5 days ago","description":"<div><div><p><i>Aurora is a global leader in the cannabis industry serving both the medical and consumer markets. Headquartered in Edmonton, Alberta, Aurora is a pioneer in global cannabis dedicated to helping people improve their lives. The Company's brand portfolio includes Aurora, Aurora Drift, San Rafael '71, Daily Special, AltaVie, MedReleaf, CanniMed, Whistler, and Reliva CBD. Providing customers with innovative, high-quality cannabis products, Aurora's brands continue to break through as industry leaders in the medical, performance, wellness and recreational markets wherever they are launched.</i></p><p><b>QUALITY CONTROL TECHNICIAN<br /></b></p><p></p><p>Whistler Medical Marijuana Corporation is a wholly owned subsidiary of Aurora Cannabis Enterprises Inc. We are currently recruiting for a Quality Control Technician to join our Facility in Pemberton, British Colombia. The incumbent will report to the Vice President of Quality and will be responsible for the following:</p><p><b>MAIN RESPONSIBILITIES:</b></p><ul><li>Understand, and follow all department SOPs and related forms to GMP and/or GPP standards, including owning QC procedures.</li><li>Understanding of Health Canada, USP, EU compliance and requirements.</li><li>Complete all required documentation using good documentation practices,</li><li>Develop and align testing specifications for all controlled materials and finished products within Aurora Cannabis standards</li><li>Maintain functional understanding of HPLC, GC-MS, ICP-MS, spectroscopy, and plant sciences</li><li>Be responsible for the execution of Quality Control process, including but not limited to:<ul><li>Material Management – sampling, testing, and approval of certificate of analysis of controlled materials. Provide guidance to procurement for suitability of material and vendors</li><li>Environmental Monitoring – participate in the development and execution of the sampling plan of grow rooms, report state of facility and procedures to minimize risk of contamination</li></ul></li><li>Compile specification documents for all tested materials, determine the disposition of the material by assessing compliance of the results to the specification</li><li>Initiate/Support investigations, to ensure ongoing compliance, to achieve process / quality improvements</li><li>Be the primary contact and liaison for all communication with outside testing labs</li><li>Be responsible for sampling and testing of cannabis products both internally and externally to ensure compliance with internal specifications and other needs</li><li>Consult and/or participate in any sampling process required at the site, with respect to suitability, and compliance</li><li>Reporting of any potential or actual deviations to Process manager and QA Manager</li><li>Effective and strong communication with all cross functional teams within the facility</li><li>Support Quality Assurance as required at the facility</li><li>Attend and participate in meetings as required</li><li>Any other suitable duties as assigned by the VP of Quality.</li></ul><br /><p></p><p></p><p><b>DESIRED QUALIFICATIONS:</b></p><ul><li>B.Sc. degree or diploma in an applicable discipline of science (chemistry, biochemistry, biology or related)</li><li>2+ years experience working in Quality Assurance</li><li>Knowledge of GMP and regulations for manufacturing and testing pharmaceutical products considered an asset</li><li>Familiarity with laboratory equipment (e.g. HPLC, GC, and ICP) considered an asset.</li><li>Proficiency in scientific writing</li><li>Strong verbal and written communication skills.</li><li>Strong computer skills. Knowledge with Microsoft excel, word and outlook</li><li>Ability to thrive in a constantly changing environment.</li><li>We would like to thank all applicants for their interest but only those selected for an interview will be contacted.</li></ul><br /><p></p><p><b>Aurora Cannabis Inc. is an Equal Opportunity Employer.</b></p></div></div>","company":{"companyType":"Public/Established","name":"Aurora Cannabis","logoUrl":"/logos/aurora-cannabis-5846417b31dc1080e3c3b4583c3f2096.png"},"location":{"country":"Canada","address":"British Columbia","stateProvince":"BC"},"frontendLink":"/job-posting/aurora-cannabis/quality-control-technician/996da8f637f19cbfb7a332f776235da1","title":"Quality Control Technician","hash":"996da8f637f19cbfb7a332f776235da1","postingUrl":"https://ca.indeed.com/job/quality-control-technician-abdb6bf7b7ecf174"},{"employmentType":"Full-time","postedOn":"6 days ago","description":"<div><p>Aurora is a global leader in the cannabis industry serving both the medical and consumer markets. Headquartered in Edmonton, Alberta, Aurora is a pioneer in global cannabis dedicated to helping people improve their lives. The Company's brand portfolio includes Aurora, Aurora Drift, San Rafael '71, Daily Special, AltaVie, MedReleaf, CanniMed, Whistler, and Reliva CBD. Providing customers with innovative, high-quality cannabis products, Aurora's brands continue to break through as industry leaders in the medical, performance, wellness and recreational markets wherever they are launched.</p><p><b>QUALITY CONTROL TECHNICIAN</b></p><p><b>Whistler Medical Marijuana Corporation is a wholly owned subsidiary of Aurora Cannabis Enterprises Inc. We are currently recruiting for a Quality Control Technician to join our Facility in Pemberton, British Colombia. The incumbent will report to the Vice President of Quality and will be responsible for the following:</b></p><p><b>MAIN RESPONSIBILITIES:</b></p><p>• Understand, and follow all department SOPs and related forms to GMP and/or GPP standards, including owning QC procedures.</p><p>• Understanding of Health Canada, USP, EU compliance and requirements.</p><p>• Complete all required documentation using good documentation practices,</p><p>• Develop and align testing specifications for all controlled materials and finished products within Aurora Cannabis standards</p><p>• Maintain functional understanding of HPLC, GC-MS, ICP-MS, spectroscopy, and plant sciences</p><p><b>• Be responsible for the execution of Quality Control process, including but not limited to:</b></p><p>• Material Management – sampling, testing, and approval of certificate of analysis of controlled materials. Provide guidance to procurement for suitability of material and vendors</p><p>• Environmental Monitoring – participate in the development and execution of the sampling plan of grow rooms, report state of facility and procedures to minimize risk of contamination</p><p>• Compile specification documents for all tested materials, determine the disposition of the material by assessing compliance of the results to the specification</p><p>• Initiate/Support investigations, to ensure ongoing compliance, to achieve process / quality improvements</p><p>• Be the primary contact and liaison for all communication with outside testing labs</p><p>• Be responsible for sampling and testing of cannabis products both internally and externally to ensure compliance with internal specifications and other needs</p><p>• Consult and/or participate in any sampling process required at the site, with respect to suitability, and compliance</p><p>• Reporting of any potential or actual deviations to Process manager and QA Manager</p><p>• Effective and strong communication with all cross functional teams within the facility</p><p>• Support Quality Assurance as required at the facility</p><p>• Attend and participate in meetings as required</p><p>• Any other suitable duties as assigned by the VP of Quality.</p><p><b>DESIRED QUALIFICATIONS:</b></p><p>• B.Sc. degree or diploma in an applicable discipline of science (chemistry, biochemistry, biology or related)</p><p>• 2+ years experience working in Quality Assurance</p><p>• Knowledge of GMP and regulations for manufacturing and testing pharmaceutical products considered an asset</p><p>• Familiarity with laboratory equipment (e.g. HPLC, GC, and ICP) considered an asset.</p><p>• Proficiency in scientific writing</p><p>• Strong verbal and written communication skills.</p><p>• Strong computer skills. Knowledge with Microsoft excel, word and outlook</p><p>• Ability to thrive in a constantly changing environment.</p><p>• We would like to thank all applicants for their interest but only those selected for an interview will be contacted.</p><p>Aurora Cannabis Inc. is an Equal Opportunity Employer</p></div>","company":{"website":"auroramj.com","companyType":"Public/Established","name":"Aurora Cannabis","logoUrl":"/logos/aurora-cannabis-5846417b31dc1080e3c3b4583c3f2096.png"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/aurora-cannabis/quality-control-technician/0608a909442dfe9b075778a3d086f8e8","title":"Quality Control Technician","hash":"0608a909442dfe9b075778a3d086f8e8","postingUrl":"https://jobs.laimoon.com/jobs/externalview/26319905"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>MJardin Group - Brampton, ON (17 hours ago) About MJardin Group: MJardin Group’s mission is to set the standard for successful ownership of assets in the cannabis industry. Our Colorado founders spent a decade refining cultivation methodology, collecting and implementing data driven standards and designing state of the art facilities. MJardin is publicly listed on the CSE (MJAR) and the QXOTC (MJARF) with offices in Denver, Colorado and Toronto, Ontario. For more information, please visit www.mjardin.com. Responsibilities: Ensure that all Standard Operating Procedures (SOPs) and Good Production Practices (GPP) for cannabis are followed. Assist the production team with Quality Assurance/Control (QA/QC) activities relative to their area. Perform quality inspections and quality checks throughout the production (various stages from seed to storage), ensure compliance as per the cannabis regulations, and report the findings to QA/Management. Work with data to determine trends or patterns that can be corrected or implemented to improve areas within the facility and report findings to QA/Management. Assist QA/QC requirements for production R&amp;D projects, if needed. Ensure compliance to process quality requirements through monitoring, documenting, and collaboration with departments. Monitor QA/QC systems. Perform other duties as directed by QA/Management. Perform quality checks for calibration and preventative maintenance of equipment Support inventory quality checks (labelling, storage, moisture content). Support review of batch documentation and compliance documents. Assist with the Pest Control Program, Sanitation Program (swab testing verification), Environmental Control Program (air sample testing), and Maintenance Program (review of products and applications). Collect internal samples (leaf tissue, water, nutrients, media, moisture content) and data to be presented/reported to QA/Management. Document test results as per SOP. Check for deviations – initiation, investigation, review, and maintenance for internal/external issues. Participate in all recall actions as required – quality checks, inventory management etc. Complete Acceptance Quality Limit (AQL) reports for all packaging materials including incoming non-cannabis materials. Support Out of Specification (OOS) or Out of Trend (OOT) results and under the direction of QA/Management. Communicate non-compliances to respective department stakeholders in a timely fashion. Qualifications: Bachelor of Science (required) 2+ years of cannabis experience (preferred) Security clearance (bonus/preferred</p></div>","company":{"website":"mjardin.com","companyType":"Public/Established","name":"MJardin Group","logoUrl":"/logos/mjardin-group-c11c9a930e9572a68088b649c99d3466.png"},"location":{"country":"Canada","address":"Brampton, ON, Canada","city":"Brampton","stateProvince":"ON"},"frontendLink":"/job-posting/mjardin-group/quality-control-lead/398e3e79f783a5b0a294d0ec1bb937fc","title":"Quality Control Lead","hash":"398e3e79f783a5b0a294d0ec1bb937fc","postingUrl":"https://ca.trabajo.org/job-649-20210428-e51431c1a423a18f93b5a22acb7b6db0"},{"employmentType":"Full-time","postedOn":"7 days ago","description":"<div><p>Green House Dispensary is currently looking to hire for QAPs (Quality Assurance Persons) to help oversee licensed cannabis production for medical and recreational marijuana purposes.</p><p>Green House Dispensary provides high-end, cannabis-infused distillates, oils and syrups. Combining our appreciation for craft cannabis with fresh local ingredients, our small-batch infusions add decadence to any meal. You can feel and taste the difference.</p><p>The Quality Assurance Person(s) position will be initially a part time-position, working remotely at first while the main location is being built. Afterward, the QAP will be required work full time on premise.</p><p>Qualifications include someone with formal education in a related science field and proven management experience in a highly regulated manufacturing environment such as: food &amp; beverage, pharmaceutical, natural health products, or other consumer goods adhering to regulatory bodies such as CFIA, Health Canada, FDA, NCR etc. This person should have experience in leading 3rd party and internal audits, recall programs, releasing products, writing and reviewing SOP’s, GMP’s, Sanitation programs and general QA / QC experience in a high volume manufacturing facility.</p><p>The QAP 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 QAP is responsible for representing the company’s QA/QC Department in all reports in relations to Health Canada.</p><p><b>Key Responsibilities:</b></p><p>• Oversees both quality control (QC) and quality assurance (QA) as per Division 1, Subdivision D and compliance with Health Canada’s QA guidelines pertaining to business, production, facility, security, storage, packaging, labeling and Good Production Practices for the ACMPR program</p><p>• Establishing and enforcing GAP, GMP, HACCP and Quality Assurance standards, providing technical and regulatory services in growing inputs, packaging and production of medical marijuana</p><p>• Supports continuous quality improvement of medical marijuana through reinforcement of product quality and food safety programs, sanitization program and oversight of security system • Ability to review regulations, documents and reports pertaining to the ACMPR, Non-confirming Reports (NCR), Corrective Action Reports (CAR), Food and Drugs Act (FDA), Controlled drugs and Substances Act (CDSA) and Pest Control Products Act (PCPA)</p><p>• Ability to develop, update and maintain Standard Operating Procedures (SOP) and Quality Manuals</p><p>• Oversee critical/technical review of documents, test results, procedures and production equipment, including equipment qualification and validation</p><p>• Review certificates of analysis and results of laboratory tests for compliance to specification</p><p>• Ensure compliance with regulations through auditing and quality systems</p><p>• Investigate product non-conformances; conduct material reviews for complaints, and document findings and responses. Manage product holds, reprocessing actions, and final disposition processes for noncompliant resources</p><p>• Manage procedures and processes pertaining to incidents, complaints, deviations and recall</p><p>• Manage audit and information requests from Health Canada pertaining to Quality Assurance and Quality Control</p><p>• Other responsibilities as assigned</p><p><b>REQUIRED QUALIFICATIONS:</b></p><p>• Bachelor of Science degree in a related technical discipline (Food, Chemical or Biological Sciences preferred)</p><p>• 4 to 5 years of experience in management of Quality Assurance in a GAP, GMP and HACCP regulated environment, with proficiency quality assurance systems, documentation, testing methods</p><p>• Knowledge, training, and experience in ACMPR requirements</p><p>• Proficient in English (proficient or functional in French is considered an asset)</p><p>• Proficient understanding of plant products and related test methodology</p><p>• Strong and current knowledge of Division 1, Subdivision 4 guidelines, Good Agricultural Practice, Good Manufacturing Practice, HACCP, Food Safety, regulatory and environmental guidelines</p><p>• General understanding of other Operational functional areas</p><p>• Experience establishing and maintaining version-controlled standards, policies, procedures and work flows</p><p>• Chemistry and Plant Biology knowledge is an asset</p><p>• *This position requires candidates to undergo security/background checks, and the individual must be approved as suitable for the QAP role</p></div>","company":{"companyType":"Private/Growth","name":"Green House Dispensary"},"location":{"country":"United States","address":"Los Angeles, CA, USA (+1 other)","city":"Los Angeles","stateProvince":"CA"},"frontendLink":"/job-posting/green-house-dispensary/quality-assurance-person/738aa9b2819286a4115287f5e1f7ccdf","title":"Quality Assurance Person","hash":"738aa9b2819286a4115287f5e1f7ccdf","postingUrl":"https://cannabisjobs.net/job/46374/quality-assurance-person/"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>Who We AreNamaste Technologies began as an international cannabis eCommerce company operating 32 sites in 20 countries. We have years of data collected on legal cannabis users and by combining machine learning technology with telemedicine apps, we’re monetizing this information. We have recently acquired our sales license for our Licensed Producer CannMart which now allows us to operate our marketplace for all brands’ legal cannabis products.CannMart operates as a subsidiary to Namaste Technologies which allows us to engage in distribution of medical cannabis through our Toronto location. This strategic acquisition leveraged our strengths in eCommerce and logistics to place us squarely in a position of leadership in the retail distribution of medical cannabis in Canada. Come and grow with one of the best cannabis companies on the planetWho You AreThe Quality Assurance Person is accountable for the management and ongoing monitoring of the quality assurance and control systems in strict compliance with the Cannabis Act and Regulations and GPP. This person should have experience in product release, review of SOP’s and work instructions, in-depth knowledge of GPP and GMP’s, Sanitation programs, in-process QC testing requirements, and general QA / QC experience in a high-volume cannabis processing, packaging and distribution facility. Experience in cannabis extraction quality management is considered an asset.HOURS OF WORK: 8:00 AM - 4:00 PM, may need to be flexible with operations on an as-needed basisRoles &amp; ResponsibilitiesOversees both quality control (QC) and quality assurance (QA) compliance with Health Canada’s guidelines pertaining to good production practices under the Cannabis Act and RegulationsReview and control of Canadian printed packaging components (including master label artwork).Ability to develop, update and maintain Standard Operating Procedures (SOP) and Work Instructions (WI)Enforcing GPP, GMP, HACCP and Quality Assurance standards, as applicableOversee critical/technical review of documents, test results, procedures and production equipment, including equipment qualification and validationReview and where necessary, perform non-conformance investigations. Manage product holds, releases, reprocessing actions, and final product dispositionComplete SOP migration project for newly licenced facilityManage audit and information requests from Health Canada pertaining to Quality Assurance and Quality Control with direction from Manager/DirectorPerform product release of all cannabis product types, including Batch Documentation Review, Certificate of Analysis Review, Label Review, Sample Handling and Release of Finished Product.Coordinate and oversee quality components of destructions and inventory management.Review and assess for compliance data from stability programs in accordance with the PCPAudits new vendors and reviews change control for adherence to site GPPs.Creates planned deviations and evaluates risk, as well as oversees subsequent updates to procedures.Representation at Health Canada Inspections, as required.Other responsibilities as assigned. EDUCATION AND EXPERIENCE:Bachelor of Science or Quality Assurance/Regulatory Affairs College Diploma Program from a recognized Canadian Institute or Equivalent.Previous experience as a QAP at a licenced producer of cannabis products, preferably one with a processing and sales licence1-3+ years relevant experience within cannabis, pharmaceuticals, food, biotech, nutraceuticals, or healthcare industries in Quality Assurance (QA).Knowledge of current Canadian GPP and Cannabis Act and Regulations and guidelines.Experience writing SOPs and document management.Investigations management experienceExperience writing scientific reports, excellent communication skills, oral and writtenQC/laboratory experience considered an assetExperience working in regulated industries, GMP considered an assetExperience using C15 considered an asset, but not a requirementWe thank you for your interest in employment opportunities at CannMart.Please note, only the candidates who are selected for an interview will be contacted. CannMart welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.Powered by JazzHR3hNpMiqdv2</p></div>","company":{"website":"namastetechnologies.com","companyType":"Public/Established","name":"Namaste Technologies","logoUrl":"/logos/namaste-technologies-9eb6b7a0098e7ad0a52503074f6bbbbd.png"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/namaste-technologies/quality-assurance-person/a6be95846c0b0ccfadff1ea4acc5cc32","title":"Quality Assurance Person","hash":"a6be95846c0b0ccfadff1ea4acc5cc32","postingUrl":"https://ca.trabajo.org/job-166-20210427-a303fa90119374940de0ed9b5740f541"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>The Opportunity Reporting directly to the Quality Assurance Manager, Cultivation, the Quality Assurance Technician performs material assessments, and duties as assigned in accordance with Part 5 – Good Production Practices of the Cannabis Regulations (SOR/2018-144), and the Food and Drug Act. Responsibilities Perform incoming material inspection and release (Cultivation) Leaf / Cannabis sample collections as necessary Support Operations Department by in-process document reviews, as applicable When required, perform visual inspection of Cannabis Review of moisture results and crop inspection results before release to PKG Read and comply with SOPs, FORMs, Work Instructions for Training Compile lot release batch records Perform periodic monitoring of ATP and moisture tests for effectiveness Inspect and release Grow &amp; Post-Harvest Rooms after change over Conduct Post-Harvest Inspections, as required Support the site environmental monitoring program with air and surface monitoring Support onboarding of new equipment (trials) Perform water sampling and coordination of testing Conduct monthly GMP Inspections (Floor walks) Collaborate / Write Non-conformance, CAPA, Planned Deviations Inspection of new equipment Act as quality representative for internal, incoming and outgoing cannabis shipments Other duties as assigned Experience Three-year college Degree or Technical Diploma at a minimum At least one-year previous experience required Ability to work independently or in a team environment Detail oriented Knowledge of Part 5 – Good Production Practices of the Cannabis Regulations (SOR/2018-144), and the Food and Drug Act preferred Spreadsheet and word processing skills Basic statistical skills Knowledge of Outlook, Word, and Excel</p></div>","company":{"website":"canopygrowth.com","companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Niagara-on-the-Lake, ON","city":"Niagara-On-The-Lake","stateProvince":"ON"},"frontendLink":"/job-posting/canopy-growth-corporation/quality-assurance-technician/a04df6a79855664a863051f7ddcf111e","title":"Quality Assurance Technician","hash":"a04df6a79855664a863051f7ddcf111e","postingUrl":"https://ca.trabajo.org/job-51-20210428-a88ed0a5f9fd7884304fa3c191509545"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>Job TitleDirector, Quality AssuranceJob Description Overview: The Director, Quality Assurance, is directly responsible for the approval and quality of cannabis throughout the growth and harvesting stages. Main responsibilities include assuring quality products and processes by establishing and enforcing quality standards and Good Manufacturing Practices (GMP) systems; implementing quality improvement initiatives to raise performance of company’s product lines; and educate and train employees as to their impact in the Quality Management System (QMS) for a licensed commercial facility.Reporting Relationships and Contacts Reports to: VP, Quality Assurance &amp; Regulatory Compliance Directs: Quality Assurance Team Internal Relationships: Cultivation, Processing, Finance, Supply Chain External Relationships: Regulatory Bodies, Vendors and Stakeholders Scope of Role: Provides oversight on the performance of all Quality Assurance (QA) personnel, practices and proceduresIs the Health Canada Compliance Manager as the primary contact for Health CanadaInitiate the development and ongoing amendment of Sundial’s Standard Operating ProceduresIs the internal compliance auditor ensuring Sundial’s compliance with all regulatory rules and regulationsEnsures that the QA practices align with Sundial’s business plan and to GMP standardsDevelops the education curriculum for training Sundial employees and Sundial’s Joint Venture and Franchise business partnersDevelops and executes product quality and yield improvement strategiesParticipates in the delivery of fee-based services to Sundial’s Joint Venture and Franchise business partnersAssures regulatory requirements are embodied in all policies, directives, practices, processes and formsEstablishes and maintains product quality documentation by writing and updating quality assurance proceduresEstablishes the following quality and reliability standards by studying their respective requirements, processes, and procedures:Raw material standardsIn-process product inspection standardsStandards for the disposition of finished productsRework standardsMaintains and improves product quality by enforcing quality assurance policies and procedures and government requirements; completing product, company, system, and compliance audits; investigating customer complaints; and collaborating with other members of management to develop new product and engineering designs as well as manufacturing and training methodsDevelops quality assurance plans by conducting hazard analyses; identifying critical control points and preventative measures; establishes critical limits, monitoring procedures, corrective actions and verification proceduresPrepares product and process quality reports by collecting, analyzing and summarizing information and trends.Enforce regulatory requirements in addition to read and be familiar with the Security Directive.Maintains quality staff by recruiting, selecting, orienting, and training employees Knowledge and Experience: Has 5-8 years of direct experience in a Quality Assurance role, leading a team of professionals in a managerial capacityHas a solid understanding of grow operations, and in particular, cannabis grow operationsMust be familiar with the Cannabis Act regulations and its relation to the Food and Drug ActBe familiar with known the Cannabis Act approved pesticides and their chemical and non-chemical approved treatments and applicationsPost-secondary education, preferably in horticulture and/or manufacturing fieldStrong background in managing budgets and financial targetsStrong business acumen, management reporting, project management and problem-solving skillsKnows how to establish excellent relationships with key stakeholdersExperience in writing reports and presentations to leadership and stakeholdersSolid background and understanding of information systems that are key to operationsProven experience in leading teams and managing performance developmentKnowledge of Occupational Health requirements for operation Required Competencies: Excellent communication and stakeholder relations skillsDemonstrated knowledge of inventory system controlsSolid team player who promotes a culture of professionalism, integrity, quality and teamworkDemonstrated ability to lead and influence the thinking and actions of othersAbility to prioritize workload in a fast-paced environmentStrong analytical and problem-solving skillsMust possess or be eligible to successfully obtain Health Canada’s Security Clearance under the Cannabis ActSolid project and time management skillsNumber of Openings1Time TypeFull time</p></div>","company":{"website":"sundialgrowers.com","companyType":"Private/Established","name":"Sundial Growers","logoUrl":"/logos/sundial-growers-70529e805ed866ef260f21921930366d.jpeg"},"location":{"country":"Canada","address":"Olds, AB (+1 other)","city":"Olds","stateProvince":"AB"},"frontendLink":"/job-posting/sundial-growers/director-quality-assurance/9c2635219417b79b198aa5219c8bafed","title":"Director, Quality Assurance","hash":"9c2635219417b79b198aa5219c8bafed","postingUrl":"https://ca.trabajo.org/job-649-20210428-e628d60c69da4304402e6318231bebce"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p><b>About Charlotte's Web:</b></p><p>Charlotte's Web products are made from our world-renowned hemp genetics grown 100% in the USA.</p><p>Founded by the Stanley Brothers of Colorado, Charlottes Web leads the industry in quality, safety, consistency and social responsibility to improve thousands of lives daily through the use of Charlotte's Web.</p><p>At Charlottes Web, we are driven by principles that extend far beyond the bottom line. It is our goal to provide products of the highest possible quality, while contributing to the sustainability of the communities we have the privilege of serving.</p><p><b>Position Summary:</b></p><p>Primary role will be to support the quality function by overseeing GMP documentation and activities involving the receipt, movement, release, and storage of materials. Lead a team of QA Associates to ensure CW products are stored and released in compliance with 21CFR111 requirements.</p><p><b>Essential Duties and Responsibilities:</b></p><p>• Oversee the QA receipt and inspection of raw materials, components intermediate materials into the warehouse</p><p>• Sample incoming raw materials upon receipt, to be sent out and tested by a contract lab</p><p>• Act as Quality contact for Material Management issues</p><p>• Assess damaged materials for quality impact using ANSI inspection guidelines</p><p>• Conduct audits of the material management process on a regular basis</p><p>• Release incoming materials through NAV (Inventory Management Software)</p><p>• Approve item masters, product specifications for materials</p><p>• Ensure KPIs are met with respect to production timing, product movement time lines, reporting of raw material usage and inventories following production</p><p>• Establish and maintain the customer returns process</p><p>• Lead the QA Recall process, conducted mock recalls a prescribed by the established SOPs</p><p>• Supervise 2-4 direct reports</p><p>• Assist with internal QA investigations, batch release, and perform other duties as assigned</p><p><b>Qualifications:</b></p><p>• Bachelors Degree in Engineering (Biomedical, Mechanical, Chemical, or Electrical) or Science (Biology)</p><p>• 4-6 years experience in a Quality Assurance role for medical device, food, dietary supplement or pharmaceutical manufacturing</p><p>• Demonstrates excellent organizational and communication skills and proficiency with the MS Office Suite, and statistical software</p><p>• Must be able to work independently with minimal supervision</p><p>• Able to prioritize projects and manage Quality Assurance resources to meet organizational goals and objectives</p><p><b>Compensation:</b></p><p>$50,800.00 - $84,800.00</p><p><b>Benefits:</b></p><p><b>We offer best-in-class benefits, including:</b></p><p>• Medical, Dental, and Vision Options</p><p>• Flexible Paid Vacation</p><p>• Up to 9 Weeks Paid Parental Leave</p><p>• Generous Employee Discount</p><p>• Employee Stock Purchase Program</p><p>• Pet Insurance</p><p>Charlottes Web provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</p><p>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Charlottes Web is an At-Will Employer.</p><p>V1.0</p></div>","company":{"companyType":"Public/Established","name":"Charlotte's Web Hemp","logoUrl":"/logos/charlottes-web-hemp-902e2edc0fd77f5d49ab925ac37fc7b6.png"},"location":{"country":"United States","address":"Louisville, CO","city":"Louisville","stateProvince":"CO"},"frontendLink":"/job-posting/charlottes-web-hemp/quality-assurance-supervisor/dc5c2e62194f38ac462a24d2b790d15f","title":"Quality Assurance Supervisor","hash":"dc5c2e62194f38ac462a24d2b790d15f","postingUrl":"https://www.linkup.com/details/2a7a035abad3bb50a3bc6a7419d0995a"},{"employmentType":"Full-time, Permanent","postedOn":"8 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></ul><ul><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></ul><ul><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: $21.00 per hour</p><p>Benefits:</p><ul><li>Dental care</li><li>Extended health care</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Experience:</p><ul><li>Quality Assurance: 1 year (preferred)</li></ul><p>Work remotely:</p><ul><li>No</li></ul><p>COVID-19 precaution(s):</p><ul><li>Remote interview process</li><li>Personal protective equipment provided or required</li><li>Temperature screenings</li><li>Social distancing guidelines in place</li><li>Sanitizing, disinfecting, or cleaning procedures in place</li></ul></div>","company":{"companyType":"Private/Established","name":"JWC","logoUrl":"/logos/jwc-d116d8ce4c4937ae6ed39bca95eacfad.jpeg"},"location":{"country":"Canada","address":"Kitchener, ON","city":"Kitchener","stateProvince":"ON"},"frontendLink":"/job-posting/jwc/quality-assurance-qa-technician/741495b072be76bad6cd9a70e9d19b98","title":"Quality Assurance (QA) Technician","hash":"741495b072be76bad6cd9a70e9d19b98","postingUrl":"https://ca.indeed.com/job/quality-assurance-qa-technician-b05caf5731fee37a"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p>The Opportunity Reporting directly to the Quality Assurance Manager, Cultivation, the Quality Assurance Technician performs material assessments, and duties as assigned in accordance with Part 5 – Good Production Practices of the Cannabis Regulations (SOR/2018-144), and the Food and Drug Act. Responsibilities Perform incoming material inspection and release (Cultivation) Leaf / Cannabis sample collections as necessary Support Operations Department by in-process document reviews, as applicable When required, perform visual inspection of Cannabis Review of moisture results and crop inspection results before release to PKG Read and comply with SOPs, FORMs, Work Instructions for Training Compile lot release batch records Perform periodic monitoring of ATP and moisture tests for effectiveness Inspect and release Grow &amp; Post-Harvest Rooms after change over Conduct Post-Harvest Inspections, as required Support the site environmental monitoring program with air and surface monitoring Support onboarding of new equipment (trials) Perform water sampling and coordination of testing Conduct monthly GMP Inspections (Floor walks) Collaborate / Write Non-conformance, CAPA, Planned Deviations Inspection of new equipment Act as quality representative for internal, incoming and outgoing cannabis shipments Other duties as assigned Experience Three-year college Degree or Technical Diploma at a minimum At least one-year previous experience required Ability to work independently or in a team environment Detail oriented Knowledge of Part 5 – Good Production Practices of the Cannabis Regulations (SOR/2018-144), and the Food and Drug Act preferred Spreadsheet and word processing skills Basic statistical skills Knowledge of Outlook, Word, and Excel</p></div>","company":{"website":"canopygrowth.com","companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Smiths Falls, ON, Canada (+1 other)","city":"Smiths Falls","stateProvince":"ON"},"frontendLink":"/job-posting/canopy-growth-corporation/quality-assurance-technician/7dc09d4b5cebbfbf8f5237c9695dbd54","title":"Quality Assurance Technician","hash":"7dc09d4b5cebbfbf8f5237c9695dbd54","postingUrl":"https://ca.directlyapply.com/jobs/canopy-growth-corporation/6087b6022f62860004507502"},{"employmentType":"Full-time","postedOn":"2 days ago","description":"<div><p>Aurora is a global leader in the cannabis industry serving both the medical and consumer markets. Headquartered in Edmonton, Alberta, Aurora is a pioneer in global cannabis dedicated to helping people improve their lives. The Company's brand portfolio includes Aurora, Aurora Drift, San Rafael '71, Daily Special, AltaVie, MedReleaf, CanniMed, Whistler, and Reliva CBD. Providing customers with innovative, high-quality cannabis products, Aurora's brands continue to break through as industry leaders in the medical, performance, wellness and recreational markets wherever they are launched. QUALITY ASSURANCE ASSOCIATE - WMMC Whistler Medical Marijuana Corp. a wholly owned subsidiary of Aurora Cannabis Inc. is currently recruiting for a Quality Assurance Associates to join our Pemberton and Whistler Facility, located in BC. The incumbent will report directly to the Manager, Quality Assurance this position will be responsible for the following: DUTIES: Represent QA as an ambassador for Cannabis Regulations, regulatory compliance with respect to GMP and company SOPs Implementation and continuous improvement of quality procedures Conduct training sessions for staff related to SOPs and general operational procedures (GMP/GPP). Perform Annual Product Review. Track metrics around compliance and efficiency and recommend measures to improve productivity and product quality. Participate in self inspection process. Conduct sanitation and pest control review to ensure compliance. Complete secondary batch review and all required follow up. CAPA review and approval, including documentation and investigation of non-conformances leading to identification of the root cause; Assigning and implementing an effective corrective and preventative action to promote continuous improvement. Responsible for compiling complaint summaries and necessary investigations. Responsible for quality assurance aspects of raw material control system. Work closely with production to ensure compliance is maintained. Assist manufacturing in drafting and writing SOPs that comply with the ACMPR and GMP. Participate in both internal and external audits as required. Assist VP Product Development and Quality Assurance as required in oversight of the facilities compliance. REQUIREMENTS 3-5 years' experience in the Quality Assurance Field Degree or diploma in a science related field Experience working in a regulated environment, pharmaceuticals, or natural health product manufacturing environment is preferred Understanding of Quality Management Systems including: batch record review, batch release, document control, change control, deviations, investigations and CAPA Fluency in MS Office is mandatory Competency of technological writing (SOPs, Annual Reports, Investigation Summary) Ability to work independently, with a strong attention to detail Ability to multitask and adapt to an evolving environment Ability to both speak and write clearly in English Whistler Medical Marijuana Corp. a wholly owned subsidiary of Aurora Cannabis Inc. is an Equal Opportunity Employer</p></div>","company":{"website":"auroramj.com","companyType":"Public/Established","name":"Aurora Cannabis","logoUrl":"/logos/aurora-cannabis-5846417b31dc1080e3c3b4583c3f2096.png"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/aurora-cannabis/quality-assurance-associate-wmmc/104cf6d86209f39c30597233d7b4a56e","title":"Quality Assurance Associate - WMMC","hash":"104cf6d86209f39c30597233d7b4a56e","postingUrl":"https://ca.trabajo.org/job-617-20210504-d307551b9405a1794410174d0c1e1b42"},{"employmentType":"Full-time","postedOn":"11 days ago","description":"<div><p>Rubicon Organics has received its cultivation and processing licenses from Health Canada and is now bringing its portfolio of Super Premium Organic Cannabis brands to market. We're looking for a talented Quality Control Specialist to help us deliver our mission and have a big impact in this high growth industry.This is an opportunity to take everything you've learned in your Quality career and continue to grow within a nimble multinational company, leaving a huge legacy in your wake.Purpose of the Quality Control Specialist role</p><p>• Control all aspects of production to ensure quality standards are met at all times</p><p>• Proactively coordinate the fundamentals of GPP, GDP, HACCP and audit programs and provide leadership and support to plant employees</p><p>• Partner with the Operations team to meet production process and product quality standards to ensure the highest quality cannabis</p><p>• Proactively coordinate the fundamentals of GPP, GDP, HACCP and audit programs and provide leadership and support to plant employees</p><p><b>Responsibilities</b></p><p>• Assist with the organoleptic grading programs for all different cannabis forms</p><p>• Assist with complaint investigations to ensure they are completed in a thorough and timely manner, and follow up on corrective actions</p><p>• Lead the continuous improvement of all quality programs by working with QA</p><p>• Oversee the collation and verification of all controlled documentation</p><p>• Oversee QC checks on receiving of raw materials, supplies, equipment, packaging components, and check documentation prior to shipping finished products (Chain of Custody, manifest)</p><p>• Ensure that QC checks in critical control points (e.g. sanitation, weight check, label check) are completed correctly and on-time</p><p>• Assist the Recall team to investigate complaints related to quality, investigate quality issues in the facility, perform audits (internal and external)</p><p>• Initiate Deviation Reports, Corrective Action and Preventive Actions (CAPAs) when investigating quality issues</p><p>• Initiate audit programs (regulatory, internal and third party)</p><p>• Manage the sampling program for analytical testing and retention samples</p><p>• Ensure that all testing is conducted in a timely fashion and within approved established procedures (E.g. Moisture Analysis, ATP testing for sanitation, environmental control swab/testing, in-house micro testing)</p><p>• Work closely with QC Technicians to resolve any quality issues arising in operational areas</p><p><b>Requirements</b></p><p>• 1-5 years of experience in a quality position within the pharmaceutical, natural health product or cannabis industries.</p><p>• Knowledge of cannabis quality metrics is considered an asset</p><p>• Experience in an ISO: 9001, ISO: 13485, ISO: 17025, or GMP environment is an asset</p><p>• Strong verbal and written communication skills</p><p>• Must be comfortable to work with employees in operational areas with diverse skill sets and level of understanding</p><p>• Proven analytical &amp; creative thinking, and adept at solving problems</p><p>• Minimum Bachelor's degree in a science related field</p><p>• Some experience with implementing label and packaging requirements in Cannabis or related industry is an asset.</p><p><b>Job Types: Full-time, PermanentSalary: $50,000.00-$60,000.00 per yearAdditional pay:</b></p><p>• Bonus pay</p><p><b>Benefits:</b></p><p>• Casual dress</p><p>• Dental care</p><p>• Disability insurance</p><p>• Extended health care</p><p>• On-site parking</p><p>• Paid time off</p><p>• Vision care</p><p><b>Schedule:</b></p><p>• Monday to Friday</p><p><b>COVID-19 considerations:</b></p><p><b>masks, sanitization, physical distancing, temperature checksExperience:</b></p><p>• QC: 2 years (Preferred)</p><p><b>Work remotely:</b></p><p>• No</p></div>","company":{"website":"rubiconorganics.com","companyType":"Public/Growth","name":"Rubicon Organics","logoUrl":"/logos/rubicon-organics-0f9dee5ab6cd7de25c3c0cd0d7513578.png"},"location":{"country":"Canada","address":"Delta, BC, Canada (+1 other)","city":"Delta","stateProvince":"BC"},"frontendLink":"/job-posting/rubicon-organics/quality-control-specialist/2be3c6eec74347d5f431912bc8ee7681","title":"Quality Control Specialist","hash":"2be3c6eec74347d5f431912bc8ee7681","postingUrl":"https://ca.mncjobz.com/jobs/quality-control-specialist-delta-891966"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p>The Opportunity An ownership stake in ensuring the web development team delivers quality user experiences to our customers. Working in a fast-paced, continuous integration environment, contributing to the development of software and web services that medical and recreational cannabis customers and Canopy Growth employees use on a daily basis. Responsibilities Participate in the design phases of the projects to provide input on quality and UX considerations Work with the developes, requestors, and Business Analysts to ensure that manual and automated testing meets requirements and acceptance criteria Evaluate existing projects and web properties and propose improvements Work with the infrastructure team to deploy testing platforms and frameworks Implement measures to proactively reveal bugs in our applications Monitor APM and fault logging facilities to proactively evaluate application performance Standardize testing environments to reflect production as closely as possible Author test cases and test plans for new and existing features/projects Write unit, integration and frontend tests to ensure adequate coverage Other duties as assigned Experience 2+ years of experience writing software tests 1+ year of experience with frontend technologies (HTML, Javascript, VueJS or others) Experience with CI/CD tools (CircleCI, Jenkins or others) Experience with frontend testing platforms (Selenium, Katalon Studio or others) Experience with software development management tools (Git, Jira, Test Rails) Experience with AWS (ECS, S3, IAM, Lambda) is desirable Experience with Bugsnag and Datadog or equivalent tools an asset Excellent communication skills. Accurate communication is critical as some team members are remote Academic degree or comparable education and work experience Python development experience a big plus</p></div>","company":{"website":"canopygrowth.com","companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Ottawa, ON, Canada (+1 other)","city":"Ottawa","stateProvince":"ON"},"frontendLink":"/job-posting/canopy-growth-corporation/web-quality-assurance/19e82ee3547862be5c6108ed0b82683c","title":"Web Quality Assurance","hash":"19e82ee3547862be5c6108ed0b82683c","postingUrl":"https://ca.directlyapply.com/jobs/canopy-growth-corporation/6087284c2f628600044e9f76"},{"postedOn":"12 days ago","description":"<div><div><p><b>THE COMPANY</b></p><p>Headquartered in Roxboro, N.C., Open Book Extracts is a cGMP-certified manufacturer of premium plant-based cannabinoid products, aiming to be the industry's true north by delivering premium products, exceptional service, and industry-leading transparency. With control of the entire supply chain, a state-of-the-art extraction campus near North Carolina's Research Triangle, proprietary refinement and conversion methods backed by a growing IP portfolio, and a team of PhD chemists and seasoned business leaders, OBX is positioned to be the trusted partner for global brands seeking to enter the marketplace. OBX Asia, with its headquarters in Hong Kong, provides strategic guidance and on-the-ground support for our Asia customers.</p><p><b>THE POSITION</b></p><p>We are seeking an experienced Quality Assurance Manager who will be responsible for managing and expanding OBX's quality assurance program which includes: industry, regulatory, and cGMP manufacturing compliance and certification programs; in-house and third party product quality testing throughout the manufacturing process; and comprehensive SOP's and employee compliance training. The QA Manager must bring a high level of energy and possess the leadership and flexibility to adapt to the evolving and infant regulatory landscape of the industry.</p><p><b>RESPONSIBILITIES</b></p><ul><li>Develop, implement, and manage the company's quality management system (QMS).</li><li>Manage third-party testing program, lab relationships, and internal and external communications in obtaining and communicating Certificate of Analyses (COA) for all batches of tested oil and finished products.</li><li>Provide thought leadership in establishing acceptable product specifications on an ongoing basis as needed to best serve the market demand and ongoing regulatory change for existing and novel products.</li><li>Ensure product quality and processes adheres to customer specifications and manufacturing requirements. Takes corrective actions to cure specification deficiencies and manage the deviation process until specification issues are resolved.</li><li>Manage the implementation of certification and compliance programs, which includes the company's ongoing cGMP compliance and audits, coordinating client and strategic partner audits. An equal emphasis shall be placed on expanding the company's certifications necessary to serve new markets or meet its new client QA requirements. This includes ISO 9001, API, EU GMP, and industry certifications as determined necessary.</li><li>Coordinate with department managers to develop, write, review and approve SOPs for the entire operation, from cultivation through finished product shipping and ensure SOPs are compliant across multiple regulatory frameworks.</li><li>Develop quality assurance plans by conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions, and verification procedures; monitoring inventories.</li><li>Develop, implement and oversee the company's HACCP (Hazard Analysis and Critical Control Points) plan.</li><li>Manage the Manufacturing Site Sanitation program, Pest control program, Pathogen Monitoring program, Food Safety, and maintain knowledge of current developments in area of expertise.</li><li>Ensure standardized tests on products meet standards and regulations regarding factors including but not limited to: labeling compliance, product quality, consistency and other factors such as chemical composition, sensory evaluation, and contaminant evaluation (microbiology, residual solvents, heavy metals, pesticides.).</li><li>Leads customer, plant and corporate communications for qualifications, complaints, audits and fill site visits. Communicates key quality information to appropriate internal personnel.</li><li>Manages daily Quality activities including supervision &amp; development of QA personnel, control of non-conforming products, Quality inspection &amp; traceability records, Measurement Systems Analysis, QA training records and lot inspection &amp; approval.</li><li>Ensure finished products meet labeling standards for hemp including compliance with FDA regulations for foods and dietary supplements, ingredients, limitations on health claims, disclaimers and warnings.</li><li>Review batch records and associated documentation, lead internal investigations and manage CAPA (Corrective Action Preventative Action) program.</li><li>Responsible for supplier qualifications/audits, vendor selection audits and all regulatory inspections.</li><li>Maintain relationships with regulatory authorities on local, state and federal levels.</li><li>General oversight of facility recordkeeping.</li></ul><p><b>EXPERIENCE</b></p><ul><li>BS or equivalent required, master's level degree in the physical sciences preferred.</li><li>QA experience in food industry / pharmaceuticals over 5 years is required with at least 2 years of those at management capacity requiring project management skills.</li><li>Experience in the cannabis industry preferred but not required.</li><li>Strong knowledge of cGMP regulations and auditing techniques.</li><li>Solid understanding of Quality Assurance cGMP requirements for global regulatory filing Experience in FDA regulated environments preferred.</li><li>Proven knowledge of ISO 9001/17025, cGMP, HACCP, FSMA, USDA and FDA regulations including labeling and nutritional facts.</li><li>Experience in analytical testing methods for potency, residual solvents, and pesticides including but not limited to HPLC, GC FID (headspace), GC-MS and LC-MS, and NMR.</li><li>High level of interpersonal skills, strong leadership abilities, organizational and time management skills.</li><li>Excellent communicator.</li><li>Ability to work independently and meet deadlines.</li></ul><p><b>OTHER DETAILS</b></p><ul><li>This is a full-time position based out of Roxboro, NC</li><li>Compensation commensurate with experience.</li><li>Background and reference checks required.</li></ul><p><b>PHYSICAL DEMANDS AND WORKING ENVIRONMENT</b></p><ul><li>Must be able to lift, carry and balance up to 50 pounds</li><li>While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions.</li><li>Ability to walk and stand for long periods of time (4-6 hours) with frequent kneeling and bending.</li><li>Working in limited climate-controlled facilities and may experience extreme heat or cold</li><li>Work with heavy fumes, plants, airborne particles and chemicals</li><li>Must be comfortable working with and around heavy machinery</li><li>May experience moderately high noise levels</li></ul><p><b>EQUAL EMPLOYMENT OPPORTUNITY STATEMENT</b></p><ul><li>Open Book Extracts is proud to be an equal opportunity employer. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.</li></ul></div></div>","company":{"companyType":"Private/Established","name":"Open Book Extracts","logoUrl":"/logos/open-book-extracts-9adc75d85be33cc6d2bb6de76bfe6348.jpeg"},"location":{"country":"United States","address":"Roxboro, NC 27573","city":"Roxboro","stateProvince":"NC"},"frontendLink":"/job-posting/open-book-extracts/quality-assurance-manager/45d376fe10d58887583c29df864a87a2","title":"Quality Assurance Manager","hash":"45d376fe10d58887583c29df864a87a2","postingUrl":"https://www.indeed.com/job/quality-assurance-manager-e9ff3d1c38d3623c"},{"employmentType":"Full-time","postedOn":"11 days ago","description":"<div><p>About the Company</p><p>Kolab Project is a platform dedicated to arts, design and culture. Our mission is to provide Canadians with a carefully curated selection of exceptional cannabis products, while championing high quality, purposeful goods produced in collaboration with culturally relevant creators.</p><p>What can you expect to do</p><p>• Embodying Auxly and Kolab’s business mission and strategy and act in a responsible, ethical, and honest behaviour while consistently leading by example.</p><p>• Verifying cannabis production processes in accordance with Kolab’s quality standards and the Cannabis Regulations.</p><p>• Sampling, assessing, and verifying critical materials, including input cannabis material, processed cannabis, and packaged cannabis product to ensure adherence to quality standards and GPP.</p><p>• Assessing sanitation procedures ahead of processing activities.</p><p>• Implementing good documentation practices to document and archive all QC results.</p><p>• Developing and maintaining quality control standard operating procedures (SOPs) and forms.</p><p>• Conducting equipment calibrations and validations, as required.</p><p>• Maintaining and performing sanitation activities on laboratory and QC equipment.</p><p>• Contributing to the creation or update of standard operating procedures, forms, and work instructions.</p><p>• Assisting with deviation investigations, implementing change control and support with related training.</p><p>• Delivering daily documentation and verified production records to the Quality team in accordance with established standards and specifications.</p><p>• Preparing for and participating in internal and external quality audits in conjunction with the Quality and Regulatory Departments.</p><p>• Promoting a healthy and safe work environment.</p><p>• Performing other duties as assigned.</p><p>What we are looking for</p><p>• Ability to work independently, prioritizes multiple projects, addresses multiple issues, and handles multiple deadlines, in a hands-on environment.</p><p>• Self-motivated with a high degree of initiative and sense of urgency.</p><p>• Experience in writing SOP’s, deviations, investigations, non-conformances and change management controls.</p><p>• Previously demonstrated solid decision-making, training, and monitoring skills.</p><p>• Strong computer skills including the use of ERP system, Microsoft Office Suite, Adobe Acrobat and Google applications.</p><p>• Strong management and leadership skills along with strategic thinking ability, and a proven track record of GMP compliance and regulatory successes.</p><p>• Effective communicator, ability to multitask, analytical and attention to detail. Excellent written and oral communication skills.</p><p>What will set you apart</p><p>• Previous experience in a manufacturing, cannabis company, or in an environment regulated by Health Canada.</p><p>• Previous experience using Sage X3.</p><p>• BSc in Biological Sciences, Pharmacy, Food or post-secondary diploma in science-related technical discipline</p><p>• Valid Health Canada Security Clearance issued under the Cannabis Act an asset.</p><p>• Previous experience in Quality Control in cannabis, food, pharmaceutical, or similar industries considered an asset</p><p>• 1 to 5 years of experience in Quality Control</p><p>• Good understanding of and experience with GPP or GMP</p><p>Kolab's leadership comprises industry first-movers, enterprising visionaries, and deep-experience specialists undeniably dedicated to creating value for our partners and the industry as a whole. Our diversified experience and proven track record ensures partners have access to an unparalleled level of real-world knowledge.</p><p>Kolab is an equal opportunity employer and encourages applications from all qualified individuals. We provide accommodation for job applicants with disabilities during the recruitment process in accordance with applicable laws. Please contact us to request accommodation.</p><p>We thank all applicants for their interest, however, only those selected for an interview will be contacted.</p><p>By submitting your interest in this job, you agree to receive text notifications with additional steps to complete your job application. You will receive up to 6 messages from the number \"63879\". Message &amp; data rates may apply. Please refer to our privacy policy for more information</p></div>","company":{"website":"kolabproject.com","companyType":"Private/Growth","name":"Kolab Project","logoUrl":"/logos/kolab-project-inc-ffc9234bc357cc76f677fdbb117d5f52.png"},"location":{"country":"Canada","address":"Carleton Place, ON, Canada","city":"Carleton Place","stateProvince":"ON"},"frontendLink":"/job-posting/kolab-project/technician-quality-control-qc/8fb9127032fdfead6fda8fc68b018dcf","title":"Technician, Quality Control (QC)","hash":"8fb9127032fdfead6fda8fc68b018dcf","postingUrl":"https://kolab-project.talentify.io/job/technician-quality-control-qc-carleton-place-on-kolab-project-1299"},{"employmentType":"Full-time","postedOn":"3 days ago","description":"<div><p>Quality Assurance Project Coordinator - Nanaimo, BC or Remote, Canada Temporary 12 month contract Monday to 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 pning five continents. Looking to develop your career at the forefront of a rapidly expanding industry? Reporting to Sr Quality Manager, the Quality Assurance Project Coordinator is responsible for integrating GMP projects, new products, and global quality management systems projects into the Site Quality Management System. Ensure projects are planned and implemented in full compliance with all ACMPR, EU GACP, GMP, GDP, GVP and 21CFR Part 11 requirements as applicable.Act as the advisor to Quality Assurance/Quality Control and operations teams on the interpretation of quality requirements at different stages of project realization. Role and Responsibilities Demonstrate a high level of autonomy and initiative, anticipating needs and addressing those needs in a timely and sensitive manner Drive implementation of IT Quality systems e.g. LIMS and Trackwise Advise Operations, with Management support on complex quality assurance questions Act as Quality point of contact for new projects, utilizing strong relationship building skills to involve appropriate stakeholders at the appropriate times Demonstrate sound judgement with how departments, processes and challenges matrix into each other and how changes in one area will impact other stakeholders Liaise with Global Quality department for planning and implementation of new contracts/business models Ensure project plans, project scope, resources and roles &amp; responsibilities are defined in accordance with the applicable regulatory requirements Ensure the needs of the different quality requirements are accounted for during concept development and project execution Collaborate with site operations and facility teams to managing risks and advocates for solutions in compliance with regulatory expectations Collaborate with business owners to ensure overall performance of the project and project completion documentation is accurate and available Report to senior management on project performance and escalate potential compliance gaps or project delays Participate in regulatory inspections and be responsible to present the quality elements of Quality Projects Qualifications and Education Requirements Undergraduate degree, preferred, Masters degree an asset or extensive experience and related training Fluent in English required (oral &amp; written) Good knowledge of GMP, working knowledge in technical development, production or QA Excellent organizational and decision-making skills Proven ability to analyze and evaluate GMP compliance Minimum 2 years of working experience in a regulated industry Must be a good team player with good communication skills Tilray welcomes applications from all qualified individuals and is committed to employment equity and diversity in the workplace</p></div>","company":{"website":"tilray.com","companyType":"Public/Established","name":"Tilray","logoUrl":"/logos/tilray-7a827f507c4afad3caee3c003054401d.png"},"location":{"country":"Canada","address":"Nanaimo, BC (+1 other)","city":"Nanaimo","stateProvince":"BC"},"frontendLink":"/job-posting/tilray/quality-assurance-project-coordinator/b37dffd8a0cabd8c8ed03dfce8de0e50","title":"Quality Assurance Project Coordinator","hash":"b37dffd8a0cabd8c8ed03dfce8de0e50","postingUrl":"https://ca.directlyapply.com/jobs/tilray/608f2be5c11aff00045c26ad"},{"employmentType":"Full-time","postedOn":"13 days ago","description":"<div><p><b>ROLE AND RESPONSIBILITIES</b></p><p>• Oversee High Park Farms Petrolia Quality Assurance department as per the Cannabis Act and Cannabis Regulations pertaining to production, processing, packaging, labeling in compliance with Good Production Practices.</p><p>• Establish and enforce Good Production Practices (GPP), Good Documentation Practices (GDP), Good Agricultural Practices (GAP), and Quality Assurance standards</p><p>• Support continuous quality improvement of High Park Farms Petrolia cannabis production and manufacturing through reinforcement of product quality programs, creation of specifications, and performance and oversight of various auditing and investigation actions</p><p>• Prepare and maintain batch records; manage batch approval and release process, including final review and batch approval</p><p>• Review regulations, documents and reports pertaining to the Cannabis Act and Cannabis Regulations.</p><p>• Participate in Health Canada inspections</p><p>• Ensure compliance with regulations through internal auditing and quality systems</p><p>• Manage and be accountable for a team of Quality Assurance staff</p><p>• Interact with production and department managers to manage a well-run quality assurance program</p><p>• Oversee preparation of Deviation Investigation Reports, including Root Cause Analysis and Corrective and Preventative Action plans</p><p>• Manage procedures and processes pertaining to change control, incidents, complaints, deviations and recalls</p><p>• Oversee the site IQ/OQ/PQ program for equipment and processes.</p><p>• Responsible for the investigation of all product related complaints.</p><p>• Resolve work problems and recommend measures to improve productivity and product quality</p><p>• Motivate members through the setting of clear expectations</p><p>• Coordinate with other supervisors, leads, and managers to obtain maximum use of resources</p><p>• Plan for manpower and equipment needs</p><p>• Ensure compliance with company standards for cost control, waste reduction, quality, safety, and complete and on-time delivery</p><p>• Provide leadership for problem and conflict resolution</p><p>• Identify and determine quality and productivity related problems and solutions</p><p>• Coordinate and oversee employee work assignments and special projects</p><p>• Maintain and adhere to all company policies and procedures</p><p>• Perform other tasks as may be assigned</p><p><b>QUALIFICATIONS AND EDUCATION REQUIREMENTS</b></p><p>• Bachelor’s degree in a technical discipline (Food, Physical, or Biological Sciences preferred)</p><p>• 3+ years of experience as a Quality Manager or Supervisor in a GPP, GMP and/or HACCP regulated environment required.</p><p>• Strong leadership and communication skills</p><p>• Direct experience participating in, managing, or conducting quality audits and inspections</p><p>• Strong and current knowledge of Good Production Practice, Good Documentation Practice</p><p>• Familiarity with the Cannabis Act and Cannabis Regulations</p><p>• Proficiency quality management systems, documentation, testing methods</p><p>• Proficient in English (proficient or functional in French is considered an asset)</p><p>• Experience establishing and maintaining version-controlled standards, policies, procedures and work flows</p><p>• Proficient understanding of plant products and related test methodology is an asset</p><p>• Chemistry and Plant Biology knowledge is an asset</p><p>• Proven ability to effectively use Microsoft Office Applications</p><p>• Must have the ability to obtain security clearance status under the Cannabis act and Cannabis Regulations</p></div>","company":{"website":"tilray.com","companyType":"Public/Established","name":"Tilray, Inc.","logoUrl":"/logos/tilray-7a827f507c4afad3caee3c003054401d.png"},"location":{"country":"United States","address":"Bridgeport, IL","city":"Bridgeport","stateProvince":"IL"},"frontendLink":"/job-posting/tilray-inc/quality-assurance-manager/5b4b07302cc947903a53e153aedaff82","title":"Quality Assurance Manager","hash":"5b4b07302cc947903a53e153aedaff82","postingUrl":"https://www.theladders.com/job/quality-assurance-manager-tilrayinc-bridgeport-il_46157133"},{"employmentType":"Full-time","postedOn":"11 days ago","description":"<div><p>QUALITY ASSURANCE ASSOCIATE Aurora Cannabis Inc. is currently recruiting for a Quality Assurance Associate to join our Edibles Manufacturing Team located in Nisku, AB. The incumbent will report directly to the Quality Assurance Manager, Edibles (West) and will be responsible for the following: MAIN RESPONSBILITIES: Participate in developing and maintaining of all required PCPs for edible cannabis product manufacturing. Create, review, and revise Standard Operating Procedures (SOPs) that comply with regulatory requirements. Investigate Complaints for Edible products. Development and Execution of Process, Equipment and Cleaning Validations. Assist in implementing continuous improvement initiatives for Edible Manufacturing. Assist in collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions and re-validations. Track metrics around compliance and efficiency for edible manufacturing and recommend measures to improve productivity and product quality. Execute QA plans by assisting in conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions and verification procedures for all edible products. Work closely with all areas of production in the facility including dried cannabis, to ensure compliance is maintained. Other duties as assigned by the QA Manager of Edibles – West. KNOWLEDGE &amp; EXPERIENCE: Degree or Diploma in Food Science or other applicable science 1+ years' relevant experience in QA in a relevant field such as food manufacturing, Natural Health Product manufacturing or Drug Product manufacturing. Experience working in a food manufacturing environment is preferred. SKILLS &amp; ABILITIES: Understanding of Quality Management Systems. Experience or an ability to demonstrate competency in GFSI and other quality management programs, including ISO 22000-2017, FSC 22000, ISO/TS 22002-series, ISO 9001-2015, GMP, HACCP, CODEX, COR, associated FSMS. Ability to interpret and understand Regulations in the context of the scientific and commercial environment. Strong written and verbal communication skills Possess strong technical writing skills. Proficiency in MS Office and experience using ERP systems. Ability to work independently, with a strong attention to detail. Ability to multitask and adapt to an evolving environment. We would like to thank all applicants for their interest but only those selected for an interview will be contacted. Aurora Cannabis Inc. is an Equal Opportunity Employer. Job Segment: Medical, Law, QA, Quality Assurance, Healthcare, Quality, Legal, Technology Apply now »</p></div>","company":{"website":"cannimed.ca","companyType":"Public/Established","name":"Cannimed By Aurora","logoUrl":"/logos/cannimed-bf99b9c93458faff6d96dc9f331679ce.png"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/cannimed-by-aurora/quality-assurance-associate/5b16f9b5c2ef1f2d812fa7b01a68c68d","title":"Quality Assurance Associate","hash":"5b16f9b5c2ef1f2d812fa7b01a68c68d","postingUrl":"https://ca.bebee.com/job/20210425-fe21184f004064bb0dfe50e8e187ee38"},{"employmentType":"Full-time","postedOn":"5 days ago","description":"<div><p>• *This role is a permanent NIGHT shift (Tues-Sat, Midnight-8AM)**</p><p>Reporting to the Quality Assurance Manager, the Quality Assurance Associate is responsible for learning, teaching, implementing, and enforcing SOP compliance in all departments. The QA/QC Associate performs quality assurance functions for products before distribution.</p><p><b>Responsibilities:</b></p><p>• Assist the Quality Assurance Manager in managing the quality management system.</p><p>• Ensure efficiency of a quality management system for all processing and packaging activities.</p><p>• Monitor process control points and take measures to eliminate deviations.</p><p>• Writes, reviews, and updates SOPs and policies to ensure continuous compliance.</p><p>• Ensures and monitors adherence to all facility SOPs relating to current GMPs and other applicable regulations, including but not limited to: change controls, deviations, recalls, returns, and customer complaints.</p><p>• Ensures and enforces good documentation practices on all applicable documents relating to GMPs.</p><p>• Responsible for training site management and employees on applicable SOPs and GMP-related topics. Responsibilities include the planning, execution, and maintenance of employee training records as well as testing to ensure training effectiveness.</p><p>• Participate in internal and external audits for Health Canada, GMP, and QA including, addressing issues, preparing response reports.</p><p>• Monitor supplier performance. Work with operations to resolve quality issues with production inputs.</p><p>• Ensure integrity of products, including oversight of annual and semi-annual inventories. Investigate variances and reconciliations.</p><p>• Oversee sampling of raw materials and finished goods for testing and retention purposes, when applicable.</p><p>• Support Site Security Officer in managing cage/vault security and access.</p><p>• Assist in the investigation and report all suspicious transactions and losses.</p><p>• Assist with the authorization, processing, and managing of all returned product.</p><p>• Assist with operational activities as required.</p><p>• Review COA's and all other private brand documents.</p><p>• Maintain SDS.</p><p><b>Qualifications:</b></p><p>• 1-2+ years of cannabis industry experience</p><p>• Bachelor of Science Degree (BSc).</p><p>• Able to successfully obtain a clear criminal record check.</p><p>• 1-2+ years of Quality Assurance work experience in a regulated industry (Cannabis, Pharma, Food Production).</p><p>• Knowledge of Health Canada cannabis regulations.</p><p>• Previous experience in either the cannabis or pharmaceutical industry.</p><p>• Strong knowledge of MS Word, Excel, and Outlook.</p><p>• Excellent analytical skills and above-average attention to detail.</p><p>• Excellent time management and prioritization skills.</p><p>• Capable of multitasking with minimal supervision.</p><p>• Excellent English communication skills, both written and verbal</p></div>","company":{"companyType":"Private/Startup","name":"Cannabis At Work","logoUrl":"/logos/cannabis-at-work-8ae63b190226a7031617f4393f916a20.jpeg"},"location":{"country":"Canada","address":"Pickering, ON","city":"Pickering","stateProvince":"ON"},"frontendLink":"/job-posting/cannabis-at-work/quality-assurance-associate-nights/f6242e2ca0b33740d637e46db925c6b0","title":"Quality Assurance Associate (Nights)","hash":"f6242e2ca0b33740d637e46db925c6b0","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-associate-nights-at-cannabis-at-work-2513125864"}]