1429 results
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Quality Manager

Venor Search Group Atholville, NB $85k - $140k - Full-time
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Since the legalization of recreational Cannabis in October 2018, HEXO Corp has experienced incredible growth.

As Canada's top Cannabis company, they continue to advance in this exciting new industry along with the incredibly talented people they have working on the team.

HEXO Corp creates globally trusted brands of easy-to-use and easy-to-understand Cannabis products.

HEXO Corp is a serious, business-oriented, and socially responsible organization that is building dynamic teams of professionals that aren't afraid to step outside their role, try new things and challenge the status quo.

Venor is proud to partner with HEXO Corp to assist in finding a candidate for the role of Quality Manager in Atholville, New Brunswick.

Reporting to the Director of Quality, as the Quality Manager you will be responsible for the implementation and executive of product quality standards for all products and processes that meet or exceed customer and internal specification, regulatory requirements and third-party requirements.

You will ensure operations at the site are operated according to Canadian Cannabis Regulations, GPP and GMP requirements, monitor process control points and take measures to eliminate deviations while providing quality coaching and support to production operations impacting on quality of product and address any issues as well as developing and executing SOP's and ensuring staff is trained on these.

As the ideal candidate, you proactively support the delivery of site objectives without compromising compliance or regulatory requirements.

You collaborate with the compliance team and regulatory bodies such as Health Canada as well as external auditors to assist in inspections, audits and potential quality, product safety and regulatory issues.

Through this collaboration, you also provide leadership, direction and guidance to Site leadership and site Quality management teams by providing direction and guidance through a thorough understanding of HEXO product safety, quality standards including regulatory requirements.

Key Responsibilities:

Conduct periodic inspections, assess risks, resolve complex issues and ensure implementation of risk elimination and/or mitigation solutions. Work with Operations and Cultivation to resolve quality issues with production inputs.

Work closely with Operations and other internal teams on change management, ensuring compliance with the Cannabis Act, GPP and QA standards throughout the process.

Ensure integrity of live and dried plant population in the HEXO Atholville facility. Investigate variances and reconciliations in the inventory program. Promote a zero-tolerance policy for non-compliance with internal/external requirements. Follow-up on deviations and apply corrective actions, working with HR and Managers on disciplinary measures as required. Hire, train and manage the Quality team members. Stay up to date on industry standards and best practices in an effort to continually improve processes and efficiency.

As the successful candidate, you have a bachelor's degree in food science or a science related discipline required, along with a minimum of eight years of experience in pharmaceutical or food based GMP operations working in Quality.

You possess five years in a Quality leadership role and have demonstrated strong leadership attributes and possess strong organizational and analytical skills.

You take pride in your work and your ability to be creative, adaptable and handle situations with a sense of urgency.

Proficiency in French is an asset, along with knowledge of Six Sigma and MS Office.

If you are interested in learning more about this great opportunity, the organization and company culture contact Erika Hildebrand via

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Work with Operations and Cultivation to resolve quality issues with production inputs.</p><p>Work closely with Operations and other internal teams on change management, ensuring compliance with the Cannabis Act, GPP and QA standards throughout the process.</p><p>Ensure integrity of live and dried plant population in the HEXO Atholville facility. Investigate variances and reconciliations in the inventory program. Promote a zero-tolerance policy for non-compliance with internal/external requirements. Follow-up on deviations and apply corrective actions, working with HR and Managers on disciplinary measures as required. Hire, train and manage the Quality team members. 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We operate best-in-class cultivation, product development, manufacturing and distribution of pharmaceutical, nutraceutical, cosmeceutical CBD products to meet the global needs of consumers and patients in fully-legal markets.</p><p>The Product and Quality Manager will be responsible for maintaining, and continuous improvement of, quality assurance and control systems to support the organization’s business operations and manufacturing processes. The candidate must have the ability to meet both external and internal regulatory requirements and expectations of production, packaging, labeling, storage and distribution of cannabis products in compliance with Cannabis Regulations. Additionally you will be current in the market and technology that affect new product development to help develop the vision, strategy and roadmap for specific product initiatives, create and introduce new products to the market based on the requirements of the customers, and in keeping with the Company’s long-term strategy.</p><p>This is a hybrid role and is perfect for the person that likes to be challenged, wear many hats, and has a strong desire to expand their skillset and knowledgebase. Candidate will work about 30% in a Quality Manager Capacity, 30% in Product Logistics, 20% in Product Development, and 20% in Regulatory Compliance. This role is expected to collaborate heavily with R&amp;D, Marketing and Operations. This is primarily a remote position but also will require occasional in person at the Chicago Office.</p><p>Desired Qualifications Include: 5+ Years experience, Degree in the Natural Sciences, Experience working in a GMP environment, Experience in cannabis sector and knowledge of cannabis regulations, Working knowledge of FDA cosmetic, food, and OTC drug regulations, Auditing and Qualifying Vendors, Drafting SOP's, Data management and Inventory Systems, Excellent Communication Skills, Generating Reports for C-Suite and BOD, Handles sensitive and proprietary information, Start-Up experience a plus, and at least basic conversational Spanish.</p><p>Even if you feel you don’t meet 100% of the qualifications but feel you could excel in this role we encourage you to apply! We are considering a wide array of candidates to find a long term addition to our team that can grow and thrive with us. Please use your cover letter to tell us what connection you have to this industry, what prompted you to apply for this position and what you hope to bring to this role!</p><p>Apply with Cover Letter and Resume</p><p>We afford equal opportunity in all phases of employment without regard to an individual's age, race, color, religion, creed, gender, national origin, citizenship status, marital status, pregnancy, sexual orientation, gender identity, gender expression, genetic information, physical or mental disability, protected veteran status or any other legally protected status.'<br />'<br />Work Location:</p><ul><li>Fully Remote</li></ul><p>Work Remotely</p><ul><li>Yes</li></ul><p>Job Type: Full-time</p><p>Pay: $30.00 - $35.00 per hour</p><p>Benefits:</p><ul><li>Health insurance</li><li>Paid time off</li></ul><p>Schedule:</p><ul><li>Monday to Friday</li></ul><p>COVID-19 considerations:<br />Our safe workplace policy mandates all employees are required to be fully vaccinated for COViD-19.</p><p>Education:</p><ul><li>Bachelor's (Required)</li></ul><p>Experience:</p><ul><li>Quality management: 1 year (Required)</li><li>Product management: 1 year (Required)</li></ul><p>Work Location: Multiple Locations</p></div>","company":{"name":"iVIK Holdings"},"location":{"country":"United States","address":"Chicago, IL","city":"Chicago","stateProvince":"IL"},"frontendLink":"/job-posting/ivik-holdings/product-and-quality-manager/715c9fe5e9be475c88844f245a1dd889","title":"Product and Quality Manager","category":"Agriculture & Farming","hash":"715c9fe5e9be475c88844f245a1dd889","postingUrl":"https://www.indeed.com/job/product-and-quality-manager-113c1008b761bb25"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"12 days ago","description":"<div><p><b>Role Summary:</b></p><p>The Cultivation Quality Manager is responsible for managing the Quality Assurance and Quality Control Supervisors and their direct reports, with responsibility for total plant health and dried cannabis flower quality, compliance, cGMPs, and executing all quality protocols to ensure plant health and dried cannabis material meet Trulieve Quality metrics. In addition, the main duties include overseeing the quality assurance functions and quality controls, supervising personnel to complete the daily tasks; full compliance with SOPs and safety requirements, administrative policies; monitoring of records, personnel development, process improvements and departmental cost performance. Responsibilities will span across all cultivation sites in Florida.</p></div>","company":{"name":"Truelieve"},"location":{"country":"United States","address":"Monticello, FL, USA","city":"Monticello","stateProvince":"FL"},"frontendLink":"/job-posting/truelieve/cultivation-quality-manager/485bf18ba9d801723c15adbe4d283500","title":"Cultivation Quality Manager","category":"Retail","hash":"485bf18ba9d801723c15adbe4d283500","postingUrl":"https://getwork.com/details/3b50c42ab0ec3fd13bc85ee2da9bff0a"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"19 days ago","description":"<div><p>Data Quality Manager works with various departments to ensure all data being generated by the laboratory is accurate and of the highest quality. Manager will oversee all aspects of data analysis and report generation and will ensure that all department objectives are met or exceeded.</p><p>Duties and Responsibilities</p><p>• Provide direct oversight of all laboratory data analysis and report generation.</p><p>• Present in monthly management meetings with weekly tasks/focus</p><p>• Oversee and manage a team of data analysts in the day-to-day use of data systems, instrument vendor software/interface and external databases such as METRC.</p><p>• Effectively and efficiently manage staff; plan and evaluate department activities.</p><p>• Develop team through recruiting and mentoring</p><p>• Define strategic goals by gathering pertinent business, financial, service, and operations information. Identify and evaluate trends, present a course of action, and evaluate outcomes.</p><p>• Identify and implement process improvements to enhance quality and mitigate risk</p><p>• Coordinate with internal teams to ensure customers are satisfied with data presentation, delivery methods, and client complaints or issues are resolved in a timely and professional manner.</p><p>• Issues statements of conformity or opinions or interpretations when necessary.</p><p>Qualification</p><p>• Must have strong analytical skills and mindset.</p><p>• Must be able to explain complex, technical information in a nontechnical, easy-to-understand way</p><p>• Must have strong interpersonal and communication skills</p><p>• Must be able to lead and delegate work effectively</p><p><b>Requirements</b></p><p>• Degree in BA/BS in STEM, information science, and/or management majors.</p><p>• MBA preferred</p><p>• Minimum of 3 years of supervisory or management experience</p><p>• Must be able to pass a background check.</p><p>• Knowledgeable of cannabis industry in Massachusetts</p><p>Welcome Please confirm that you're over</p><p>21 years old to continue</p></div>","company":{"companyType":"Private/Growth","name":"MCR Labs","logoUrl":"/logos/mcr-labs-aed09bd7c5f16aa5e7ebc524f087c747.jpeg"},"location":{"country":"United States","address":"United States"},"frontendLink":"/job-posting/mcr-labs/data-quality-manager/dbaf1f351a4a6eb6edcba1ff3edd9f47","title":"Data Quality Manager","category":"Medical & Healthcare","hash":"dbaf1f351a4a6eb6edcba1ff3edd9f47","postingUrl":"https://us.bebee.com/job/20211002-50854e8b1bd078fa58d55d74b9a673b3"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"3 days ago","description":"<div><div><b>PHM Brands</b><br /><br /><b>TITLE:</b> Quality Assurance Manager<br /><br /><b>LOCATION:</b> Champaign, IL<br /><br /><b>DATE POSTED:</b> 10/5/2021<br /><br /><b>SALARY:</b> Based on Experience<br /><br /><b>DESCRIPTION:</b> The Quality Assurance Manager is responsible for providing leadership to the quality assurance team and manages all food/product safety, quality programs, and laboratory activities of the facility. Manage and oversee the entire plant's food safety and quality control functions consistent with FSMA requirements, GFSI standards, Food Safety principles, allergen controls and GMP practices. Review raw material and finished products for compliance to regulation and specification. Active leader in ensuring all aspects of the plant' s Food Safety programs and Regulatory Compliance are maintained to the highest standards. Participate in ongoing review and evaluation of the plant' s GFSI program as a GFSI Leader and assist in employee training of GFSI principles and pre-requisite programs. Manage and oversee daily laboratory functions, Sanitation and Pest Control activities. The Quality Assurance Manager will be based out of Monticello, IL.<br /><br /><b>QUALIFICATIONS:</b><br /><ul><li>Bachelor's Degree in Food Science or equivalent experience, food process engineering, or appropriate biological sciences. Certified in a GFSI Scheme a plus.</li><li>Three to five (3-5) years of professional work-related experience in quality assurance and or quality control and food safety out of the food industry.</li><li>Previous experience in the CBD industry preferred, but not required.</li><li>Preventative Controls for Food Safety Qualified Individual (PCQI Certified).</li><li>Three years to five years' experience with HACCP / Quality Assurance Programs.</li><li>Ability to manage an hourly staff and interface with various levels of Management.</li><li>Ability to read, analyze, and interpret general food industry periodicals, professional journals and government regulations.</li><li>Ability to produce reports, business correspondence and procedure Read, write, and speak English fluently.</li><li>Intermediate or above knowledge of Microsoft Word, Excel, and PowerPoint software programs. Proficient in use of various \"mainframe\" data management systems and</li><li>Ability to resolve practical problems and deal with a variety of variables.</li><li>Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule</li><li>Ability to calculate figures, analyze financial reports, determine processing rates work with percentages and fractional calculations.</li><li>Strong knowledge of Food GMP's, SOP's, HACCP/Food Safety, CBD, Regulatory and Environmental</li><li>Experience with Organic, Kosher, and API (Active Pharmaceutical Ingredient) certification and</li><li>Ability to meet attendance</li><li>Ability to maintain an effective working relationship with all internal and external contacts.</li><li>Understanding of basic principles of the GFSI programs and other food safety policies/procedures.</li><br /><b>PHYSICAL DEMANDS:</b><br /><ul><li>Rotating and oscillating equipment</li><li>Exposure to manufacturing equipment hazards, especially forklifts</li><li>Standing and walking on concrete floor</li><li>Exposure to raw hemp biomass</li><br /><b>BENEFIT SUMMARY:</b><br /><br />Medical, Dental, Vision, Company Paid LI, AD&amp;D, Matching 401K, Employee Assistance Program, Paid Time off<br /><br />PHM Brandsis an equal opportunity employer and considers qualified applicants for employment without regard to sex, race, color, religion, ethnic or national origin, gender, sexual orientation, gender identity or expression, age, pregnancy, leave status, disability, veteran status, genetic information and/or any other characteristic or status protected by national, federal, state, or local law.<br /><br />PM21</ul></ul><p><br />PI150464087</p></div></div>","company":{"companyType":"Private/Established","name":"PHM Brands","logoUrl":"/logos/phm-brands-llc-871151ce94e5c9812b99a6fbd0d48599.png"},"location":{"country":"United States","address":"Champaign, IL 61820","city":"Champaign","stateProvince":"IL"},"frontendLink":"/job-posting/phm-brands/quality-assurance-manager/80dd458f3e7fc0eb4f21b862d3760af8","title":"Quality Assurance Manager","category":"Professional, Scientific, and Technical Services","hash":"80dd458f3e7fc0eb4f21b862d3760af8","postingUrl":"https://www.indeed.com/job/quality-assurance-manager-07ba7d5052e5153f"},{"salaries":[{"salaryStart":"$32","salaryEnd":"$49","currency":"","source":"ERI Economic Research Institute","position":"Quality Assurance Specialist","type":"per hour","url":"https://www.erieri.com/salary/job/quality-assurance-specialist/canada/ontario/chatham-kent"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"2 days ago","description":"<div><p>Quality Assurance Associate - Processing Leamington ON. Monday-Friday 11 : 00PM-7 : 30AM About Tilray Tilray is a global pioneer in cannabis research, cultivation, processing and distribution currently serving tens of thousands of patients in ten countries spanning five continents.</p><p>Looking to develop your career at the forefront of a rapidly expanding industry? Job Summary : Reporting to the Quality Assurance Supervisor, this position will be responsible for supporting Tilray's Quality Assurance team in the cultivation department.</p><p>As industry leaders committed to offering clean, safe, and pure cannabis products, we engage in a collaborative culture that is fast paced, dynamic and highly motivating.</p><p>If you’re looking to thrive in a new, rapidly growing and innovative space, we would love to hear from you. We are currently seeking a strong leader to join our Quality team.</p><p>This position will be Monday-Friday with some required Saturdays on a rotational swing shift of 6 : 30AM-3 00PM &amp; 3 : 00PM-11 : 30PM.</p><p><b>Your day-to-day responsibilities will consist of :</b></p><p>• Continually monitor processing areas for GPP regulatory requirements under the Cannabis Act and Cannabis Regulations and their associated regulations such as those for Natural Health Products.</p><p>• Assist all functional departments on establishing systems to eliminate GACP / GPP gaps that relate to Processing and manufacturing</p><p>• Support and maintain systems to ensure quality of products as defined through internal Good Production Practices and established Standard Operating Procedures.</p><p>• Communicate, educate and support the quality requirements to all operational departments.</p><p>• Create, review and maintain Standard Operational Procedures, investigate non-conformances / deviations and customer complaints as it relates to quality.</p><p>• Participate in the initiation and writing of change controls to controlled documents as needed to ensure defined quality objectives are met</p><p>• Coordinate and conduct new hire and ongoing GPP / GACP training.</p><p>• Read, understand and follow safe work procedures</p><p>• Other duties as assigned</p><p><b>To be successful in this position you will have the following :</b></p><p>• A combination of bachelor’s degree in science related field and / or technical Diploma from an accredited post-secondary institution.</p><p>• Quality experience in a horticulture, food or health product environment is preferred</p><p>• Knowledge of plant science, pest management, GPP / GACP (Good Production Practices / Good Agricultural and Collection Practices) or GMP (Good manufacturing Practices) would be considered an asset</p><p>• Superior communication and writing skills</p><p>• Self-starter, critical thinker and team oriented</p><p>• High work ethic standards are a must</p><p>• Exceptional attention to detail</p><p>• Candidates must be able to work swing shift hours (two weeks days 6 : 30 am-3 : 00 pm, two weeks afternoons 8 : 30am-5 : 00pm).</p><p>Weekend coverage may be required.</p><p>Due to the nature of the business and working with controlled substances, all new employees will be required to complete a background check prior to starting work.</p><p>This may include : verifying work references, validating all credentials and criminal record checks.</p><p>It is a requirement that the selected Candidate be legally eligible to work in Canada at the time an offer is presented.</p><p>Internal Candidates : For any internal applicants, we ask that you bring a hard copy of your resume with a supporting cover letter to the Human Resources Office, send a direct email to our Talent Acquisition Specialist or apply online at https : / / www.</p><p>tilray.com / careers Note : The statements above are intended to describe the general nature and level of work being performed by people assigned to the job.</p><p>They are not constructed to be an exhaustive list of responsibilities, duties and skills required of personnel in the job.</p><p>Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer.</p><p>Tilray is committed to providing an accessible and barrier-free environment. Please advise Human Resources if you require accommodation during any part of the recruitment process</p></div>","company":{"website":"tilray.com","companyType":"Public/Established","name":"Tilray","logoUrl":"/logos/tilray-7a827f507c4afad3caee3c003054401d.png"},"location":{"country":"Canada","address":"Leamington, ON","city":"Leamington","stateProvince":"ON"},"frontendLink":"/job-posting/tilray/quality-assurance-associate/1016eb997ca610f5e9b1d904c4f6b748","title":"Quality Assurance Associate","category":"Medical & Healthcare","hash":"1016eb997ca610f5e9b1d904c4f6b748","postingUrl":"https://ca.talent.com/view?id=02f198da6b98","salary":"$32 - $49"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"11 days ago","description":"<div><p>Located in Barrie, Ontario, MediPharm Labs offers a professional and collaborative workplace culture in a leading-edge facility built to international pharma standards. Our company is a recognized leader in the Cannabis industry, named Start-Up of the Year at the most recent Canadian Cannabis Awards. Our growing team of scientists, technicians, engineers and business professionals delivers quality and innovation through research, discipline, and forward thinking.</p><p>The Quality Control Manager will maintain quality standards by approving incoming materials, in-process production, finished products (in house and 3rd party testing), and recording the results. Manage, lead and mentor a team of Quality Control Associates, Chemists and Leads</p><p>• Oversee approval or rejection of starting materials, packaging materials, intermediate, bulk and finished products;</p><p>• Ensure that all necessary testing is carried out and the associated records evaluated</p><p>• Approve specifications, sampling instructions test methods and other Quality Control procedures</p><p>• Approve and monitor any contract analysts and external laboratories</p><p>• Ensure the qualification and maintenance of the department, premises and equipment</p><p>• Ensure that the appropriate Quality Control validations are executed, including process validation as required</p><p>• Ensure that the required initial and continuing training of the department personnel is carried out and adapted according to need</p><p>• Participate in the design, effective implementation, monitoring and maintenance of the quality management system, including the authorization of applicable written procedures and other documents and to ensure their strict implementation.</p><p>• Oversee the monitoring and control of the manufacturing environment, including compliance to the facility hygiene program</p><p>• Continuous monitoring of material suppliers, contract manufacturers and providers of other GMP related outsourced activities</p><p>• Ensure the designation and monitoring of storage conditions for materials and products is followed</p><p>• Ensure compliance for retention of records</p><p>• Ensure compliance with GMP/GPP regulations as required by Health Canada or other jurisdictions to obtain/maintain GMP/GPP status</p><p>• Oversee the inspection, investigation, and taking of samples, in order to monitor factors which may affect product quality</p><p>• Participate in management reviews of process performance, product quality and of the quality management system and advocating continual improvement</p><p>• Ensure a timely and effective communication and escalation process exists to raise quality issues to the appropriate levels of management</p><p>• Oversee the control of the reference and/or retention samples of materials and products when applicable</p><p>• Ensure the correct labelling of containers of materials and products</p><p>• Ensure the monitoring of the stability of the products</p><p>• Participate in the investigation of complaints related to the quality of the product, etc.</p><p>• Perform Annual Product Quality Review in conjunction with the Quality Management team</p><p>• Manage all aspects of the raw material receiving and inspection program, ensuring all incoming materials are approved by confirming specifications, conducting any required tests, controlling the status of all materials</p><p>• Manage the approval in-process production by confirming required specifications, conducting visual and measurement tests, and communicating the required adjustments to the Production Manager</p><p>• Manage in-house testing of finished products and other samples by conducting required tests, data review and issuance of CofA’s</p><p>• Manage all aspects of testing performed by 3rd party testing labs: sample delivery, testing plans, confirmation of receipt, CofA delivery commitments, 3rd party lab performance, investigations and method transfers</p><p>• Oversee the return of products for re-work if needed and complete documentation to confirm re-work</p><p>• Manage the Quality Control team, championing and promoting a quality culture within the company</p><p>• Lead the qualification of new and existing lab instrumentation</p><p>• Timely review and investigation of all OOS, OOL and OOT results</p><p><b>Skills and Qualifications needed for the position:</b></p><p>• Bachelor’s degree in chemistry or science related field, or equivalent</p><p>• Strong work ethic and integrity</p><p>• Proven experience leading a Quality Control laboratory, preferably within the pharmaceutical or related GMP environment</p><p>• Experience in raw material testing and release</p><p>• Experience in technical writing</p><p>• Excellent time management skills with the ability to work under minimal supervision</p><p>• Competent data analysis and data management skills</p><p>• Experience in OOS (out of specification) investigation</p><p>• Excellent knowledge of GC (Gas chromatography) and HPLC (High performance liquid chromatography) and other analytical, wet chemistry and general laboratory techniques</p><p>• Excellent technical competence and software proficiency including MS Office and lab instrumentation software</p><p>• Strong communication skills, including the ability to explain and teach methodologies</p><p><b>At MediPharm Labs we offer comprehensive health and dental benefits, 3 weeks’ vacation and the following opportunities:</b></p><p>• Be part of the foundation of a new, growing industry and make your mark</p><p>• Autonomy and key decision-making opportunities</p><p>• Work in a fast-paced, collaborative environment with opportunity for growth both personally and professionally</p><p>MediPharm Labs is committed to providing accommodation for applicants with disabilities in its recruitment processes. If you require accommodation at any time during the recruitment process, please contact 705-719-7425 ext. 1080</p></div>","company":{"website":"medipharmlabs.com","companyType":"Private/Established","name":"Medipharm Labs Inc","logoUrl":"/logos/medipharm-labs-4315d12381f59d368d5becaecc808e0c.jpeg"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/medipharm-labs-inc/quality-control-manager/dc28286083d57ff83740ebcef20ee534","title":"Quality Control Manager","category":"Medical & Healthcare","hash":"dc28286083d57ff83740ebcef20ee534","postingUrl":"https://grabjobs.co/canada/job/full-time/manufacturing/quality-control-manager-6037367"},{"salaries":[{"salaryStart":"$57k","salaryEnd":"$93k","currency":"","source":"PayScale","position":"Software Quality Assurance (SQA) Lead Tester","type":"per year","url":"https://www.payscale.com/research/CA/Job=Software_Quality_Assurance_(SQA)_Lead_Tester/Salary/8242f4ef/Toronto-ON"},{"salaryStart":"$50k","salaryEnd":"$63k","currency":"","source":"Glassdoor","position":"QA Analyst","type":"per year","url":"https://www.glassdoor.ca/Salary/LifeWorks-QA-Analyst-Toronto-Salaries-EJI_IE443726.0,9_KO10,20_IL.21,28_IM976.htm"},{"salaryStart":"$46","salaryEnd":"$73","currency":"","source":"ERI Economic Research Institute","position":"Quality Assurance Manager","type":"per hour","url":"https://www.erieri.com/salary/job/quality-assurance-manager/canada/ontario/burlington"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"5 days ago","description":"<div><p>Quality Assurance Person (QAP) Location: Bradford, ON Overview: Reporting to the Manager, Quality Assurance the Quality Assurance Person is responsible for Good Production Practices (GPP) according to Health Canada and Good Manufacturing Practices within the corporate Quality Management System (QMS). Integrate, over-see, maintain, and report actual conformance status in the following areas: GMP, GPP Compliance, Training and Awareness Batch Release, both Domestic and International Internal Audit Program QAP Task Transfer Monitoring Recall Program Pest Control Program Clinical Trials Preventive Control Plan, as assigned Product Development and/or Operations Trials, as assigned Provide technical guidance and oversight in partnership with the Quality Assurance Manager in the following areas: Product Compliance External Audits Annual Product Quality Review Preventive Control Plans Quality Risk Management Product Non-conformance or OOS Primary Job Responsibilities: Assess, interpret, and ensure compliance with applicable regulations and/or other governing bodies Assess cannabis and controlled material test methods to ensure compliance for intended market Inform Quality Manager and/or Department of critical regulatory changes, or potential gaps Co-lead Health Canada and/or other external audits in partnership with QAM Provide technical directive and decision making in partnership with the QAM Review and approval of all controlled documents related to product/process Assure the release of Cannabis Products according to SOPs for all markets Collaborate with Quality Assurance Specialist as needed to ensure effective Stability program Support product recall in conjunction with Quality Assurance, Control, and other stakeholders Review Pest Control Reports Monthly review and sign-off of complaints Sign-off of NCR or CAPA with direct impact to Product Quality Sign-off complaints, non-conformances, CAPAs, pest control reports, changes related to GPP etc., Stays up to date on technical Quality Assurance practices within the industry and abroad Maintain security and confidentiality of all aspects of the business Adhere to Aurora SOPs and comply with Health Canada Cannabis Act and EU GMP as applicable Other duties as required Job Requirements: Bachelor’s, Master’s Degree in Science, Pharmacology, Medical Laboratory and/or combined work experience. Security cleared individual according to Canadian Cannabis Act and regulations Currently or previously a Health Canada approved Quality Assurance Person or Alternate Quality Assurance Person (considered an asset) A minimum three to five years of quality assurance experience preferred, preferred technical quality with experience releasing batches Keeps up with scientific knowledge, compliance and industry demands Demonstrated ability to work with others as a member of a team. Knowledge of health and safety standards and compliance. Strong communication and interpersonal skills required to communicate with the department supervisors and workers to insure seamless and transparent evaluation of in-process data and operations. Demonstrated ability to understand and execute verbal and written instructions. Proficiency to prioritize activities. Demonstrated problem solving skills and attention to detail. Capability to maintain both physical and mental fitness and alertness. Position requires ability to work at various levels of height and move freely and independently throughout all areas and levels of the building (including climbing stairs) to work in areas of production, labs, offices and others as required. We would like to thank all applications for their interest but only those selected for an interview will be contacted. Aurora is an equal opportunity employer. At Aurora, we are committed to do business inclusively and accommodate applicants with disabilities. If you require accommodation (including, but not limited to, an accessible interview site, alternate format of job posting) during the recruitment and selection process, please let our Recruitment team know</p></div>","company":{"website":"auroramj.com","companyType":"Public/Established","name":"Aurora Cannabis","logoUrl":"/logos/aurora-cannabis-5846417b31dc1080e3c3b4583c3f2096.png"},"location":{"country":"Canada","address":"Bradford West Gwillimbury, ON","city":"Bradford West Gwillimbury","stateProvince":"ON"},"frontendLink":"/job-posting/aurora-cannabis/quality-assurance-person/e84bcc392d67c304d2c23882e04d632c","title":"Quality Assurance Person","category":"Medical & Healthcare","hash":"e84bcc392d67c304d2c23882e04d632c","postingUrl":"https://www.rapidinterviews.com/job/quality-assurance-person-with-aurora-cannabis-in-bradford-west-gwillimbury-tal-0307","salary":"$57k - $93k"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"5 days ago","description":"<div><p><b>Technician, Quality Assurance - Fenwick</b></p><p><b>Who We Are</b><br />Winner of 7 Canadian Cannabis Awards - Including Best Licensed Producer 2018! This quite possibly is the best company to work for in the world!<br />CannTrust - a front-runner in the cannabis industry, is a federally regulated licensed producer, publicly traded, and a proudly Canadian company. CannTrust is leading the Canadian and global market in producing standardized cannabis products. CannTrust is ready for Cannabis 2.0 and is currently developing new products that span the medical, recreational, beauty, wellness, and pet markets.<br />CannTrust is committed to research and innovation, as well as contributing to the growing body of evidence-based research regarding the use and efficacy of cannabis. Its product development teams along with its global pharma partner, are diligently innovating and developing products that will make it easier for patients to use medical cannabis. CannTrust supports ongoing patient education about medical cannabis and has a compassionate use program to support patients with financial needs.</p><p><b>Who You Are</b><br />The ideal candidate is an agile, business savvy individual who is committed to getting better everyday. You are a passionate influencer with strong communication skills, who is open to giving and receiving feedback. You are customer-centric with an ability to act as a mentor amongst your peers. Of course, you also deliver consistent results by aligning yourself with CannTrust values.</p><p><b>Roles &amp; Responsibilities</b></p><ul><li>Ensure quality and compliance processes within Grow areas, Harvest, Dry/Cure rooms, Manual Groom area, production, and packaging of dried Cannabis</li></ul><ul><li>Support to manage day-to-day operations in compliance with CannTrust quality system requirements and Good Manufacturing Practices and support the implementation of process efficiencies.</li></ul><ul><li>Ensure through shop floor presence and knowledge transfer, that there is in-depth GMP understanding as it pertains to operations and that issues are identified and dealt with through close contact with cross-functional departments</li></ul><ul><li>Perform shop floor process walkabouts and facilities shop floor walkabouts; support operations to remediate issues that are identified</li></ul><ul><li>Perform batch record review in real time on the shop floor</li></ul><ul><li>Perform spot checks, sampling, line clearance, sanitation verification and in process testing</li></ul><ul><li>Assist with deviation and out of specification investigations, corrective and preventative actions, and change controls as required</li></ul><ul><li>Ensure inspection/audit readiness at all times and contribute to GMP inspections and follow up correspondence</li></ul><ul><li>Perform audits in conjunction with the Internal Auditor</li></ul><ul><li>Support operational activities as related to, examples:</li></ul><ul><li>Trouble shooting quality issues</li></ul><ul><li>Make recommendations to improve efficiencies and productivity</li></ul><p><b>Individual Influencer</b></p><ul><li>Customer-centric – always searching for ways to improve service, takes action to resolve (internal or external) customer issues.</li></ul><ul><li>Acts as a mentor to peers and cross functional partners.</li></ul><ul><li>Follows through on commitments, adheres to deadlines.</li></ul><ul><li>Uses good judgment about when to act independently or escalate an issue.</li></ul><ul><li>Acts with Integrity: Demonstrates responsible, ethical, and honest behavior while consistently leading by example.</li></ul><ul><li>Motivates operations to take timely action, and works to resolve escalations in a timely manner</li></ul><ul><li>Monitors progress to departmental goals with company strategy</li></ul><ul><li>Supports achievement of department goals &amp; objectives</li></ul><ul><li>Complies with all company policies</li></ul><ul><li>Delivers results while staying aligned with CannTrust Values.</li></ul><p><b>Education &amp; Experience</b></p><ul><li>B.Sc. in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Engineering (or related field).</li></ul><ul><li>Minimum 3 - 5 years’ experience in quality assurance or related area within the pharmaceutical, healthcare or food/beverage industry.</li></ul><ul><li>Experience in manufacturing operations, laboratory operations, document control, and quality management systems (deviation, CAPA, change control, batch record review).</li></ul><ul><li>Understanding of equipment, manufacturing processes, maintenance, and quality standards.</li></ul><ul><li>Demonstrated and thorough knowledge of GMP relative to Health Canada, FDA, and other global regulations.</li></ul><ul><li>Knowledge of ACMPR, ISO, HACCP, GFSI, or other quality systems is an asset.</li></ul><p><b>Requirements</b></p><ul><li>Ability to influence without authority</li></ul><ul><li>Proficiency in Microsoft Outlook, Word, Excel, PowerPoint</li></ul><ul><li>Organizational Skills – Ability to work in a fast-paced environment</li></ul><ul><li>Professionalism – Demonstrate professional standards of conduct</li></ul><ul><li>Accountability – Take pride in the work that is accomplished and understand the function/ process flow for the larger picture.</li></ul><ul><li>Communication – Express and transmit information with consistency and clarity.</li></ul><ul><li>Attention to Detail – Attend to details and pursue quality in the accomplishment of tasks</li></ul><ul><li>Adaptability – Able to respond to changing conditions, priorities, technology, and requirements.</li></ul><ul><li>Teamwork – Works cooperatively and effectively with others to reach a common goal.</li></ul><ul><li>Available to work variously weekday and/or weekend shifts, which may fluctuate. Your shift schedule may be subject to change based on business needs and customer demand</li></ul><p><b>Physical Demands</b><br />While performing the responsibilities of the job, the employee is required to be able to lift up to and including 50lbs, sit and/or stand for extended periods of time and reach with arms/hands. Walking, standing, bending, stooping, reaching, twisting, lifting, pushing, pulling, and moving items is occasionally required.</p><p><b>Work Environment</b><br />While performing the duties of this job, the employee is exposed to packaged cannabis products/supplies. The working environment can be noisy at times and temperate, the employee must have knowledge of how to manage their own personal safety under these conditions.</p><p>CannTrust is an equal opportunity employer. We thank you for your interest in employment opportunities at CannTrust. Please note, only the candidates who are selected for an interview will be contacted. CannTrust welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.</p><p>Job Type: Full-time</p><p>Work Location: Multiple Locations</p></div>","company":{"companyType":"Public/Established","name":"CannTrust","logoUrl":"/logos/canntrust-d201bb4ca139eb0b36f0ce0af7b71eca.png"},"location":{"country":"Canada","address":"Fenwick, ON","city":"Fenwick","stateProvince":"ON"},"frontendLink":"/job-posting/canntrust/technician-quality-assurance/776265b43a8c7e3af9aed9ef2587bc03","title":"Technician, Quality Assurance","category":"Medical & Healthcare","hash":"776265b43a8c7e3af9aed9ef2587bc03","postingUrl":"https://ca.indeed.com/job/technician-quality-assurance-593c47bd5c311268"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"12 days ago","description":"<div><p></p><div><div><p>Located in Barrie, Ontario, MediPharm Labs offers a professional and collaborative workplace culture in a leading-edge facility built to international pharma standards. Our company is a recognized leader in the Cannabis industry, named <i>Start-Up of the Year</i> at the most recent Canadian Cannabis Awards. Our growing team of scientists, technicians, engineers and business professionals delivers quality and innovation through research, discipline, and forward thinking.</p><p>The Quality Control Manager will maintain quality standards by approving incoming materials, in-process production, finished products (in house and 3rd party testing), and recording the results. Manage, lead and mentor a team of Quality Control Associates, Chemists and Leads</p><ul><li>Oversee approval or rejection of starting materials, packaging materials, intermediate, bulk and finished products;</li><li>Ensure that all necessary testing is carried out and the associated records evaluated</li><li>Approve specifications, sampling instructions, test methods and other Quality Control procedures</li><li>Approve and monitor any contract analysts and external laboratories</li><li>Ensure the qualification and maintenance of the department, premises and equipment</li><li>Ensure that the appropriate Quality Control validations are executed, including process validation as required</li><li>Ensure that the required initial and continuing training of the department personnel is carried out and adapted according to need</li><li>Participate in the design, effective implementation, monitoring and maintenance of the quality management system, including the authorization of applicable written procedures and other documents and to ensure their strict implementation.</li><li>Oversee the monitoring and control of the manufacturing environment, including compliance to the facility hygiene program</li><li>Continuous monitoring of material suppliers, contract manufacturers and providers of other GMP related outsourced activities</li><li>Ensure the designation and monitoring of storage conditions for materials and products is followed</li><li>Ensure compliance for retention of records</li><li>Ensure compliance with GMP/GPP regulations as required by Health Canada or other jurisdictions to obtain/maintain GMP/GPP status</li><li>Oversee the inspection, investigation, and taking of samples, in order to monitor factors which may affect product quality</li><li>Participate in management reviews of process performance, product quality and of the quality management system and advocating continual improvement</li><li>Ensure a timely and effective communication and escalation process exists to raise quality issues to the appropriate levels of management</li><li>Oversee the control of the reference and/or retention samples of materials and products when applicable</li><li>Ensure the correct labelling of containers of materials and products</li><li>Ensure the monitoring of the stability of the products</li><li>Participate in the investigation of complaints related to the quality of the product, etc.</li><li>Perform Annual Product Quality Review in conjunction with the Quality Management team</li><li>Manage all aspects of the raw material receiving and inspection program, ensuring all incoming materials are approved by confirming specifications, conducting any required tests, controlling the status of all materials</li><li>Manage the approval in-process production by confirming required specifications, conducting visual and measurement tests, and communicating the required adjustments to the Production Manager</li><li>Manage in-house testing of finished products and other samples by conducting required tests, data review and issuance of CofA’s</li><li>Manage all aspects of testing performed by 3rd party testing labs: sample delivery, testing plans, confirmation of receipt, CofA delivery commitments, 3rd party lab performance, investigations and method transfers</li><li>Oversee the return of products for re-work if needed and complete documentation to confirm re-work</li><li>Manage the Quality Control team, championing and promoting a quality culture within the company</li><li>Lead the qualification of new and existing lab instrumentation</li><li>Timely review and investigation of all OOS, OOL and OOT results</li></ul><br /><p></p><p><b>Skills and Qualifications needed for the position:</b></p><ul><li>Bachelor’s degree in chemistry or science related field, or equivalent</li></ul><ul><li>Strong work ethic and integrity</li><li>Proven experience leading a Quality Control laboratory, preferably within the pharmaceutical or related GMP environment</li><li>Experience in raw material testing and release</li><li>Experience in technical writing</li><li>Excellent time management skills with the ability to work under minimal supervision</li><li>Competent data analysis and data management skills</li><li>Experience in OOS (out of specification) investigation</li><li>Excellent knowledge of GC (Gas chromatography) and HPLC (High performance liquid chromatography) and other analytical, wet chemistry and general laboratory techniques</li><li>Excellent technical competence and software proficiency including MS Office and lab instrumentation software</li><li>Strong communication skills, including the ability to explain and teach methodologies</li></ul><br /><p></p></div><p></p><div><p>At MediPharm Labs we offer comprehensive health and dental benefits, 3 weeks’ vacation and the following opportunities:</p><ul><li>Be part of the foundation of a new, growing industry and make your mark</li><li>Autonomy and key decision-making opportunities</li><li>Work in a fast-paced, collaborative environment with opportunity for growth both personally and professionally</li></ul><p>MediPharm Labs is committed to providing accommodation for applicants with disabilities in its recruitment processes. If you require accommodation at any time during the recruitment process, please contact <span><a href=\"tel:+1-705-719-7425\">705-719-7425 ext. 1080</a></span>.</p></div></div><p></p></div>","company":{"companyType":"Private/Established","name":"MediPharm Labs","logoUrl":"/logos/medipharm-labs-4315d12381f59d368d5becaecc808e0c.jpeg"},"location":{"country":"Canada","address":"Barrie, ON","city":"Barrie","stateProvince":"ON"},"frontendLink":"/job-posting/medipharm-labs/quality-control-manager/5f7576677710c0bccc66b611087ebb76","title":"Quality Control Manager","category":"Medical & Healthcare","hash":"5f7576677710c0bccc66b611087ebb76","postingUrl":"https://ca.indeed.com/job/quality-control-manager-ce645370ff33d24f"},{"employmentType":"Full-time, Permanent","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"7 days ago","description":"<div><p>Our client is searching for a <b>Quality Assurance Manager/Person</b> who will be responsible for building and managing the Quality Assurance team. You will build upon an existing Quality Management System to implement quality processes, systems, and relationships and drive best in class quality and performance.</p><p>You will act as the primary <b>Quality Assurance Person (QAP) </b>on the license, overseeing testing, review, and release of all products entering the market.</p><p><b>Responsibilities: </b></p><ul><li>Act as the primary QAP on the site license(s), as designated by Health Canada:</li></ul><ul><li>Approve all Standard Operating Procedures (SOPs) for site activities.</li></ul><ul><li>Establish and approve a Preventive Control Plan (PCP) for all applicable activities prior to their implementation.</li></ul><ul><li>Approve all finished product lots prior to sale.</li></ul><ul><li>Review and approve all packaging and labeling for compliance with Cannabis Regulations.</li></ul><ul><li>Review and approve all third-party analytical test results against established specifications.</li></ul><ul><li>Investigate all out-of-specification results and coordinate follow-up.</li></ul><ul><li>Oversee customer complaint programs and investigate each complaint with regards to the quality of cannabis.</li></ul><ul><li>Coordinate product recall and recall simulations.</li></ul><ul><li>Manage/lead and represent the company in virtual and physical audits - including inspections performed by Health Canada and any other regulatory agencies.</li></ul><ul><li>Work with external suppliers and contract labs to ensure Quality Agreements are up to date and are effective in supporting launch and commercialized operations.</li></ul><ul><li>Provide QA guidance to product development projects and technical transfer activities where applicable.</li></ul><ul><li>Hire great people and help to assign work and provide feedback &amp; coaching to team members within the Quality Assurance department.</li></ul><ul><li>Coordinate and execute periodic self-auditing of the site Quality Management System and trend analysis of all aspects of GPP operations.</li></ul><ul><li>Identify and initiate improvements to the quality management system, ensuring compliance to all relevant quality standards and regulatory requirements.</li></ul><ul><li>as well as site regulatory inspection preparation and internal site audit program.</li></ul><ul><li>Ensure the facility or facilities are in a constant state of inspection readiness across all functions through continuous improvement, education, training, and internal audits.</li></ul><ul><li>Oversee teams responsible for document management such as change control, deviations, non-conformance reports, and quality investigations.</li></ul><ul><li>Ensure effective coordination of investigations, root cause analysis, risk assessments and implementation of change control and corrective and preventive actions.</li></ul><p><b>Qualifications and Experience: </b></p><ul><li>B.Sc. required, in a scientific/technical discipline with 7+ years of experience in a quality position within the Cannabis, CPG, or pharmaceutical industries.</li></ul><ul><li>5+ years in a management/leadership role with experience in managing both large and small teams.</li></ul><ul><li>Highly familiar with the Cannabis Act and applicable regulatory requirements in combination with detailed knowledge of GDP and GPP in the Cannabis industry.</li></ul><ul><li>Knowledgeable and high level of historical experience in being the primary lead for supplier quality audits, complaint investigations, Health Canada regulatory audits, and quality compliance risk assessments.</li></ul><ul><li>Experience in both startup/early phase and commercial GMP manufacturing organizations.</li></ul><ul><li>Excellent working knowledge and experience with the practical implementation of HC, FDA and EMA regulations and guidelines in relation to manufacturing of Cannabis.</li></ul><ul><li>Exceptional interpersonal skills including the ability to influence behaviors and negotiate and resolve challenges with poise, tact, and diplomacy.</li></ul><ul><li>Exceptional oral and written communication skills.</li></ul><ul><li>Extensive experience with managing regulatory inspections and client audits.</li></ul><ul><li>Strong organizational skills and are able to prioritize and manage complex processes/ projects.</li></ul><ul><li>The ability to define problems, collect data, and draw valid conclusions using science and mathematics.</li></ul><ul><li>Confidence in your decision making and the ability to think strategically.</li></ul><ul><li>Entrepreneurial drive that allows you to evaluate and improve business outcomes.</li></ul><ul><li>Creative problem solver and be confident in finding ways to improve QA and operational processes.</li></ul><ul><li>Have the ability to identify and mitigate business risks before they happen.</li></ul><p><i>We appreciate the interest from all candidates; however, we will be contacting only those that best fit our client’s requirements.</i></p><p><i>Terra Recruitment welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.</i></p><p>Job Types: Full-time, Permanent</p><p>Salary: $1.00 per year</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>Ability to commute/relocate:</p><ul><li>Red Deer, AB: reliably commute or be willing to relocate with an employer-provided relocation package (preferred)</li></ul><p>Education:</p><ul><li>Bachelor's Degree (preferred)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 5 years (preferred)</li><li>cannabis industry: 4 years (preferred)</li></ul><p>Licence/Certification:</p><ul><li>Health Canada Security Clearance (preferred)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"name":"Terra Recruitment Inc."},"location":{"country":"Canada","address":"Red Deer, AB","city":"Red Deer","stateProvince":"AB"},"frontendLink":"/job-posting/terra-recruitment-inc/quality-assurance-manager-qap/5e656d5c0748d18de47baa83518fcf4f","title":"Quality Assurance Manager/QAP","category":"Manufacturing","hash":"5e656d5c0748d18de47baa83518fcf4f","postingUrl":"https://ca.indeed.com/job/quality-assurance-managerqap-546b7b5f35651ab4"},{"salaries":[{"salaryStart":"$46k","salaryEnd":"$110k","currency":"US","source":"Glassdoor","position":"QA Lead","type":"per year","url":"https://www.glassdoor.com/Salaries/portland-qa-lead-salary-SRCH_IL.0,8_IM700_KO9,16.htm"},{"salaryStart":"$66k","salaryEnd":"$110k","currency":"US","source":"Salary.com","position":"Test Lead","type":"per year","url":"https://www.salary.com/research/salary/posting/test-lead-salary/portland-or"},{"salaryStart":"$25k","salaryEnd":"$48k","currency":"US","source":"ZipRecruiter","position":"Quality Assurance Technician","type":"per year","url":"https://www.ziprecruiter.com/Salaries/Quality-Assurance-Technician-Salary-in-Portland,OR"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"3 days ago","description":"<div><p>Phylos is a crop science company using modern molecular genetics and computational biology to breed the next generation of hemp and cannabis. Since 2014 we have supported grower success with genetic testing products offering unparalleled accuracy and reliability. We are a new generation of plant scientists, transforming the hemp and cannabis industries with elite seeds and clones. By leveraging our deep expertise in the cannabis genome, we are unlocking the potential of this plant to be grown at scale, providing cultivators in every region with the varieties, tools, and expertise to drive business growth. POSITION SUMMARY: As the Quality Lead, you will be assisting in all aspects of Quality systems development, execution, and continuous improvement. You will work in collaboration with cross-functional teams to improve and implement processes while meeting regulatory compliance standards and company goals. You are a proactive, solutions oriented thinker and you love finding ways to standardize and improve processes. This position is temporarily remote. RESPONSIBILITIES: Perform analysis of products, deviations, process changes, CAPAs, technology transfers, and other metrics to identify trends and provide recommendations to Quality Management for continuous improvement. Draft, review, approve, and maintain controlled documents, validation plans, change controls, equipment inspections, safety documentation, and scientific reports as needed. Assist in all aspects of Quality Systems development and in program execution and enhancement. Provide direction, motivation, and leadership to the Quality Team as recommended by Quality Management. Assess customer requirements and ensure that these are met. Respond to customer inquiries or complaints as needed. Assist in monitoring/validating current and new internal procedures for accuracy and efficiency. Lead weekly Quality team meetings and provide project updates to Quality management. Schedule, conduct, and analyze findings for internal audits where applicable, to ensure compliance to current SOPs, processes, and/or regulatory requirements. Compile monthly, quarterly, and annual metrics relating to Quality for Quality Management review. Assist with training programs for new employees and maintain training records. Design and provide recurring training on quality procedures and company best practices as needed. Review and suggest new software and tools to reduce waste, facilitate continuous improvement, encourage cross-functional workflows QC all internal software deploys for SIMS to ensure accuracy. Pro-actively encourages continuous improvement and daily problem-solving initiatives to increase operational effectiveness and efficiency. Responsible for organizing and maintaining the testing schedule for Seed Co., certification renewal, and international shipment documentation records. QUALIFICATIONS: BS/BA in Biology, Agriculture, Chemistry and/or other related fields preferred. 3 years of professional experience in Quality Assurance. Knowledge of ISO 9001, ISO 17025, GMP, and GLP preferred. Ability to develop and follow protocols, policies and procedures with exactness. Strong communication and organizational skills with ability to work on multiple priorities at once with high attention to detail. Proven experience in implementing processes in collaboration with cross functional teams. Strong analytical and technical writing skills. Current experience with MS Office, Google Suite, and Smartsheet or similar project management system. Ability to sit and stand for prolonged periods. Ability to perform repetitive motions with hands and arms. Comfortable in a fast-paced environment. Must be a self-starter demonstrating initiative with the ability to work in an independent and organized manner. Working knowledge of Quality systems required. We have been honored to receive inquiries for our positions from all over the world. In order to have the best possible outcome in the hiring process, we would like to make sure that you are aware that: 1. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. 2. Given the current status of cannabis in the US, if you are not a US citizen, there is a possibility that this association may jeopardize the status of your VISA, and/or your ability to exit and reenter the United States. If this is a concern for you, please contact your immigration attorney regarding this potential risk prior to proceeding with your application Monthly updates with the latest news, events, and helpful resources</p></div>","company":{"website":"phylos.bio","name":"Phylos Bioscience, Inc."},"location":{"country":"United States","address":"Portland, OR, USA","city":"Portland","stateProvince":"OR"},"frontendLink":"/job-posting/phylos-bioscience-inc/quality-lead/a3a869c65897833266f7cdd1a99945ac","title":"Quality Lead","category":"Agriculture & Farming","hash":"a3a869c65897833266f7cdd1a99945ac","postingUrl":"https://www.recruit.net/job/quality-lead-jobs/BD739AE6430AC649","salary":"$46k - $110k"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"7 days ago","description":"<div><p>VIVO Cannabis™ is recognized for trusted, premium cannabis products and services. It holds production and sales licences from Health Canada and operates world-class indoor and seasonal airhouse cultivation facilities. VIVO has a collection of premium brands, each targeting different customer segments, including Canna Farms™, Beacon Medical™, Fireside™, Fireside-X™, Lumina™ and Canadian Bud Collection™. Harvest Medicine, VIVO's patient-centric, scalable network of medical cannabis clinics, has serviced over 150,000 patient visits. VIVO is pursuing several partnership and product development opportunities and is focusing its international efforts on Germany and Australia. The Opportunity Are you a champion of quality processes and standards? Are you passionate about ensuring the products that are delivered to market are in compliance with appropriate quality regulations? Do you have exceptional attention to detail, document writing and record keeping capacity? Are you eager to learn and be part of a dynamic business in a fast-paced industry? If so keep reading to learn about an exciting new opportunity to join VIVO Cannabis on our journey to create, grow and deliver excellence outcomes in the cannabis space focused primarily on health and wellness Position Overview VIVO’s licensed producer, Canna Farms Inc, located in Hope BC is seeking a methodical, conscientious and innovative Quality Assurance Technician to support all aspects of quality assurance. Key Responsibilities Assist the Quality Manager in managing the Quality Management System (QMS) Ensure compliance with the Cannabis Act, Controlled Drugs and Substances Act (CDSA), Narcotics Control Regulations (NCR), Pest Control Products Act (PCPA), Fertilizer Act, GPP/GMP, and HACCP, and other relevant legislation and standards Write, review, and update Standard Operating Procedures (SOPs) and quality policies/procedures to ensure continuous compliance with the Cannabis Act Support continuous quality improvement initiatives Enforcing established SOPs and all health &amp; safety protocols and workplace policies to ensure consistent quality of all cannabis products, including but not limited to, dried cannabis, cannabis oil, and live cannabis plants Conduct quality control checks for in-process and finished products and assist with internal audit program; documenting, correcting, and preventing any deviations Update computer records/ERP and/or perform required calculations as needed Participation in analytical investigations of out-of-specification (OOS) results, including examination of results, generation of deviation reports, root-cause analysis, and implementation of corrective and preventative actions (CAPA) Analysis of reports and QC data to identify trends, and if necessary, recommend revisions to quality standards and procedures Reporting of potential or actual process/specification deviations Identify and report potential or actual process/specification deviations Assist in preparation of quality related reports (CAPA, Deviation and Investigation) Review lot coding and tracking of individual plants and the resultant harvested bulk and finished products and update computer records/ERP Perform review of documents from all within facility departments Evaluate and approve sanitation of equipment and production areas and ensure all products are free of contamination Qualifications and Skills Academic/Educational Requirements University/College Degree/Diploma OR Equivalent Professional Experience in a natural or applied science (e.g., chemistry, biology, food/pharmaceutical sciences or a related field) Required Skills/Experience/Knowledge University/College Degree/Diploma OR Equivalent Professional Experience in a natural or applied science (e.g., chemistry, biology, food/pharmaceutical sciences or a related field 1-3+ years’ experience in the Legal Cannabis, Agriculture, Food, or Pharmaceutical Industry Knowledge, training, and experience in Good Production Practices (GPP) and/or Good Manufacturing Practices (GMP) is considered a significant asset Knowledge of analytical chemistry/microbiology and extraction systems is considered an asset Previous experience working in a regulated production environment Excellent attention to detail Excellent critical thinking and assessment skills Excellent English communication skills (written and verbal) Knowledge of quality assurance terminology, methods, and tools Strong organizational skills, including the ability to manage time, set priorities, and multi-task Strong verbal and written communication skills; Strong organizational skills; ability to efficiently manage time and competing priorities Customer-centric commercial driven mindset Positive can-do attitude; entrepreneurial spirit with a bias for action Champion of high-performance culture through engagement with company’s performance management process and provision of meaningful feedback Ability to thrive &amp; succeed in a fast-paced growth environment High degree of collaboration working cross functionally and geographically Excellent learning agility with a hunger to become knowledgeable in the space Excellent quantitative analytical skills; Excel power-user; proficient in Microsoft 365 applications (PowerPoint, Word) Previous Health Canada Security Clearance and work experience with a Canadian Licensed Producer (LP) is considered as an asset Must be able to obtain and maintain a security clearance, as per Health Canada's Cannabis Act VIVO Competencies &amp; Values Unity – We know great outcomes in business aren’t accomplished by one person, they are accomplished by a team, success for us hinges on collaboration Accountability – We take ownership and have a bias for action that allows us to produce excellent customer-centric results Integrity – We know it’s this simple, wrong is wrong even if everyone is doing it, right is right even if no one is doing it Innovation – We strive to identify and embrace opportunities to differentiate and elevate the experience of our customers and our employees Self-Awareness – We embrace reflection and feedback so our growth and development thrives Leadership – We know authenticity in our interactions and empowering those around us makes us valued leaders no matter our position</p></div>","company":{"website":"cannafarms.ca","companyType":"Private/Established","name":"Canna Farms","logoUrl":"/logos/canna-farms-ltd-3c74a1cafb40aca11ffc2c9195637faa.png"},"location":{"country":"Canada","address":"Fraser Valley, BC","city":"Fraser Valley","stateProvince":"BC"},"frontendLink":"/job-posting/canna-farms/quality-assurance-technician/d99822ce536e1314ab02c05e83dc5ca0","title":"Quality Assurance Technician","category":"Medical & Healthcare","hash":"d99822ce536e1314ab02c05e83dc5ca0","postingUrl":"https://ca.trabajo.org/job-166-20211013-bc8471c9e299c2043e5e20d77daa07fe"},{"salaries":[],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"9 days ago","description":"<div><p><b>Position Summary:</b></p><p>The Quality Assurance Manager is responsible for management of all quality system related activities. In addition, the QA Manager is responsible for coordinating, facilitating, and implementing quality assurance standards based on Company, AZDHS and FDA GAP requirements across all Company products and related processes. This position will write quality assurance SOPs and policies, develop and control early-stage quality programs, monitor suppliers/CRO conformance with QA standards and procedures and set their direction for regulatory compliance.</p><p>Why does this role exist? To monitor the process and understand all areas of quality assurance and the risk or hazards that can adversely affect the quality of the product.</p><p>How does this role contribute to the mission? The Quality Assurance Manager ensures the quality of the product that leaves the facility meets AZDHS requirements and is safe, amenable and protects the consumer (patient).</p><p>How will your role be measured Success will be measured by the frequency of quality-based returns and defects. As the system and process is continually improved, there will be a tremendous reduction in the amount of returns. The processes put in place will assure a uniform and consistent product across the board. Our customers will know what to expect and the production facility will then be able to deliver on those expectations on a regular basis.</p><p><b>Essential Duties and Responsibilities:</b></p><p>• Define quality strategic direction and drive continuous improvement efforts.</p><p>• Must stay current with regulatory compliance requirements applicable to the industry such as AZDHS, FDA, USDA, and OSHA regulations by conducting research on such matters utilizing regulatory publications and web sites</p><p>• Investigate and track customer complaints regarding quality as well as work with external customers (from operations to senior management) to resolve quality issues.</p><p>• Product Monitoring (From seed to sell and return) - Evaluate and document product quality and rate products in accordance with specifications and metrics at various stages of process.</p><p>• Report deficiencies to the assigned Supervisor for corrective action by initiating a non-conformance report and reviewing at CAPA meetings.</p><p>• Conduct Internal Quality Audits and Quality Evaluations by inspecting assigned facility based on pre-established criteria, documenting and reporting deficiencies to the assigned Supervisor for corrective action</p><p>• Assist and train others in QMS document control, writing and revisions, including routing and/or approval of change request packages.</p><p>• Reviews batch documentation, test results, and good documentation and record-keeping practices.</p><p>• Discusses issues and concerns directly with cultivation agent and cultivation operations management so any corrections and improvements can be made in a timely manner.</p><p>• Collaborates with operational functions to troubleshoot product defects, provides advice with process improvements to eliminate errors and reduce risk.</p><p>• Consolidates technical information from cultivation operations and prepares written investigation and CAPA reports which may be provided to AZDHS.</p><p>• Monitors compliance to established Good Manufacturing Practice (GMP &amp; cGMP)</p><p>• Prepare Monthly QA Review reports</p><p>• Support continuous improvement through teamwork, shared best practices and personnel and self -development.</p><p>• Develop and implement AZDHS compliant lab sampling protocol and program. Work with the Lab Manager assuring timely and accurate reporting of lab data while meeting.</p><p>• Formulate and maintain quality assurance objectives and coordinate objectives with production procedures in cooperation with other plant managers to maximize product reliability and minimize costs.</p><p>• Investigate and track customer complaints regarding quality.</p><p>• Develop and analyze statistical data and product specifications to determine present standards and establish proposed quality and reliability expectancy of finished product.</p><p>• Supervises accurate and timely reporting of HACCP and work documentations and records to ensure integrity and retention requirements.</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• Direct workers engaged in inspection and testing activities to ensure continuous control over materials and products.</p><p>• Ownership of quality KPIs and develop action plans to improve.</p><p>• Plan, promote, and organize training activities related to product quality and reliability.</p><p>• Investigate and track customer complaints regarding quality.</p><p>• Write, update, and maintain Quality SOP's (Standard Operating Procedures).</p><p>• Review other departmental SOP’s and Work Instructions for validity, clarity, and accuracy.</p><p>• Improve system by conducting hazard analysis; studying and creating process flow charts; recommending modifications in workflow, workstations and product; developing new procedures; recommending equipment modifications and purchases.</p><p>• Reduce waste by studying guidelines, methods, equipment, and operator techniques; recommending changes; identifying and analyzing waste.</p><p>• Work with staff to prepare quality assurance information and reports by collecting, analyzing and summarizing information and trends and provide feedback and interpretation to production management and staff.</p><p>• Maintain and improve Quality Management Systems database by writing computer programs; entering, verifying, and securing data.</p><p>• Maintain operations guidelines by writing and updating policies, procedures and methods including but not limited to standard operating procedures, quality assurance manuals, testing procedures, methodologies or criteria to determine usefulness.</p><p>• Improve quality assurance job knowledge by attending educational workshops; reviewing professional publications and studies; establishing personal networks; benchmarking state-of-the-art practices; participating in professional societies.</p><p>• Provide direct reports with effective leadership through development and implementation of daily/weekly work plan, effective communication, provide necessary training, recognize and reward good performance, identify performance deficiencies and take corrective action when necessary.</p><p>• Oversee and assist in HACCP.</p><p><b>Job Requirements:</b></p><p>• The Arizona Medical Marijuana Act (the “Act”) stipulates that candidate must be at least 21 years of age or older, and successfully pass a criminal background investigation and fingerprint clearance conducted by state authorities. Additionally, the Act requires that candidates apply for and obtain a valid dispensary agent registration card prior to commencing employment at either a dispensary or any of its cultivation sites.</p><p>• Bachelor’s degree (or foreign equivalent) in a related field or equivalent job experience.</p><p>• Experience in organizing and managing Quality Management Systems, HACCP plan implementation and monitoring. Solid people management experience, strong written and verbal communication skills, including writing non-conformance reports and executive summaries and communicating with senior level operations, quality management team, and regulatory agencies</p><p>• Familiar with the regulatory requirements, AZDHS, ADEQ, FDA, USDA, OSHA</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>• Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA</p><p>• HACCP Certification. Additional certs a plus i.e. GFSI, ISO 9001, PCQI, ISO 22000</p><p>• Sound knowledge of the practical application of statistical methods (SPS Charts/Graphs) to determine whether processes and results are appropriate.</p><p>• Strong organizational skills &amp; Advanced problem-solving skills</p><p>• Effective communication skills In English (Verbal, Reading and Writing); Bilingual (English/Spanish) a plus</p><p>• Strong computer proficiency including Microsoft Office Suite (Outlook, Word, Excel, PowerPoint) and data base programs, statistical process control, analytical instrumentations and quantitative analysis reporting.</p><p>• You Must Possess a current Driver’s License (minimum Class D) and have own vehicle to travel to various sites, several times a day.</p><p>• Ability to successfully complete a post-offer / pre-employment Drug and Alcohol Screening.</p><p>• Ability to stand and sit for prolonged periods of time, as this position will be working in both an office setting and a manufacturing work site.</p><p>• Ability to withstand differing temperatures, as the greenhouse is hot and humid, and the manufacturing area is cold and dry.</p><p>• Ability to lift up to 25 lbs. frequently, to move and grade product.</p><p>• Ability to visually assess product for grading and defects, ability to communicate verbally and written to report results.</p><p><b>Compensation:</b></p><p>• $60k - $80k base salary (negotiable)</p><p>• Benefits / medical, vision and dental</p><p>• Paid holidays</p><p>• Flexible PTO</p><p>• Recognition and rewards for a job well done</p><p>• A fun and focused team atmosphere</p><p>• Casual dress</p><p>• Open to relocation if not in Willcox, AZ</p><p><b>About Vangst:</b></p><p>Vangst is a venture backed, high growth recruiting technology company. We have revolutionized the fastest growing industry in the world by connecting thousands of professionals with careers in cannabis. Through technology and a world-class team, Vangst supplies the cannabis industry with the best talent.</p><p>Vangst is an equal opportunity employer and 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 characters protected by the law. This job description is a product of Vangst</p></div>","company":{"companyType":"Private/Established","name":"Vangst","logoUrl":"/logos/vangst-1731290886786334fb502ebdee566cc6.png"},"location":{"country":"United States","address":"Willcox, AZ, USA","city":"Willcox","stateProvince":"AZ"},"frontendLink":"/job-posting/vangst/quality-assurance-manager/4024890982603e70469a0451799f71c1","title":"Quality Assurance Manager","category":"Professional, Scientific, and Technical Services","hash":"4024890982603e70469a0451799f71c1","postingUrl":"https://www.linkedin.com/jobs/view/quality-assurance-manager-at-vangst-2747358363"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"6 hours ago","description":"<div><div><p><b>Location:</b> Franklin, MA</p><p></p><p><b><br />PARALLEL</b></p><p></p><p><b><br />Everyone is welcome here</b>. Each of us is unique, and that’s what makes us amazing. We believe in inclusiveness and celebrating each person’s individuality, because there’s power in bringing people with different points of view and life experiences together. That’s why we provide equal employment opportunities (EEO). All applicants are considered regardless of race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, or sexual orientation.</p><p></p><p><br />So, bring yourself and your best ideas; when we feel safe and comfortable being ourselves, there’s no limit to what we can achieve.</p><p></p><p><b><br />IN A NUTSHELL…</b></p><p></p><p><br />This role is to help drive the teams towards the day’s goals and help them prioritize or switch gears when necessary. Inventory Specialists play a critical role in ensuring that all monitoring of inventory is compliant with all RMD regulations.</p><p></p><p><br />This role is with NETA, one of the renowned retail brands under the Parallel umbrella. Parallel is one of the largest multi-state cannabis companies in the world, owning and operating in five markets; Florida (Surterra Wellness), Massachusetts (NETA), Pennsylvania (Goodblend), Nevada (The Apothecary Shoppe) and Texas (Surterra Wellness). If you enjoy companies that are growing, moving fast, and constantly challenging themselves to achieve more, then Parallel is for you. We work hard, lean on each other, and are passionate about a pretty ambitious vision … pioneering a new paradigm of what well-being can be for all people, everywhere. For more information, visit www.liveparallel.com.<br /></p><p></p><br /><p><b>WHAT YOU WILL BE DOING</b></p><p></p><ul><li><br />Daily maintenance of menu decisions, product storage, intake, and continuous live tracking with internal systems.</li><li>Provide product expertise and knowledge to PSAs and explain the potential benefits of various type products and strains of medical marijuana, as well as methods of use.</li><li>Responsible for performing any quality control checks as directed by the Inventory Director, Supervisor, Coordinator, or Dispensary Manager.</li><li>Responsible for accepting, tracking and processing all returns that occur at the point of sale; and daily reconciliation process.</li><li>Accurately perform inventory management, including processing product deliveries and restocking sales stations.</li><li>Maintain organized and consistent stocking and packaging systems for both existing and new products.</li><li>Communicate information to dispensary operation teams regarding inventory locations and any changes throughout the day. EXPERIENCE AND SKILLS YOU’LL BRING</li></ul><p></p><p><b><br />Required</b></p><p></p><ul><li>Age 21 or over</li><li>High school Diploma or equivalent</li><li>Valid Government-Issued Photo ID</li></ul><p></p><p><b><br />Preferred</b></p><p></p><ul><li>Strong communication skills.</li><li>Prior experience with Seed to Sale Systems or Virtual Gateway software.</li><li>Demonstrated ability to address situations and problem solve.</li><li>Must have full time open availability, every weekend availability.</li><li>Strong attention to detail, organizational skills and time management abilities.</li><li>Proficiency in windows-based software and Internet navigation.<br /></li></ul><p></p><br /><p><b>PHYSICAL REQUIREMENTS</b></p><p></p><ul><li><br />Ability to lift up to 50 lbs on occasion.</li><li>Ability to be able to be in constant standing/moving position.</li><li>Constantly operates a computer and other office productivity machinery.</li><li>The person in this position frequently communicates with other employees/customers.<br /></li></ul><p></p><br /><p><b>YOU WILL BE SUCCESSFUL IF YOU…</b></p><p></p><ul><li><br />Are self-motivated; micro-managing isn’t fun for anyone</li><li>Roll your sleeves up and do the work; strategy is important, but so is getting stuff done</li><li>Can work fast and be flexible; our industry is always changing</li><li>Play nice with others; we collaborate with each other a lot</li><li>Think creatively; sometimes, the “traditional” solution isn’t the best one</li></ul><p></p><p><b><br />WHAT YOU GET</b></p><p></p><ul><li><br />Consistent, reliable benefits; Full medical/vision/dental, 401k with possibility of a company match, access to company-sponsored well-being programs</li><li>Personal growth; industry-leading leadership and professional development offerings</li><li>Balance and flexibility; paid time off, paid parental leave, flexible work arrangements</li><li>Belonging and voice; employee resource groups, product advisory councils, monthly opportunities to share feedback and discuss your employee experience</li><li>Chance to make a difference; Employee Relief Fund, community volunteerism through our Parallel Cares program</li><li>Equity opportunity; ability to share in both the short-term and the long-term financial success of Parallel</li><li>Employee discount</li></ul><p></p><p><b><br />PARALLEL IS UNITED BY OUR VISION, MISSION, &amp; VALUES</b></p><p></p><p><b><br />Our Vision – </b>why we exist – is to pioneer well-being and improve the quality of life for humanity through the benefits of cannabinoids.</p><p><b>Our Mission –</b> how we will do this – is to build a leading, global well-being company through the best talent, our values, trusted and recognized brands, science and technology-based innovation, and a relentless focus on execution and continuous improvement.</p><p><b>Our Values –</b> Integrity | Collaboration | Alignment | Intentionality | Accountability | Agility</p><p></p><p><b><br />We are an Equal Opportunity Employer.</b> We embrace and encourage our employees’ differences in age, color, disability, ethnicity, gender identity or expression, language, national origin, physical and mental ability, political affiliation, race, religion, sexual orientation, socioeconomic status, veteran status, and other characteristics that make our employees unique.</p><p></p><p><b><br />DISCLAIMER</b></p><p></p><p><br />Parallel reserves the right to change or assign other duties to this job description. Your employment with Parallel is a voluntary one and is subject to termination by you or Parallel at will, with or without cause, and with or without notice, at any time. Nothing in this document shall be interpreted to be in conflict with or to eliminate or modify in any way the employment-at-will status of Parallel associates.</p><br />Internal ID: 43912_20211019</div></div>","company":{"companyType":"Public/Growth","name":"Neta"},"location":{"country":"United States","address":"Franklin, MA 02038","city":"Franklin","stateProvince":"MA"},"frontendLink":"/job-posting/neta/2247-quality-assurance-specialist/0f3a0365b9daa95c6720e0d0710b7be7","title":"2247 - Quality Assurance Specialist","category":"Professional, Scientific, and Technical Services","hash":"0f3a0365b9daa95c6720e0d0710b7be7","postingUrl":"https://www.indeed.com/job/2247-quality-assurance-specialist-439fec5f850d27ca"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"14 days ago","description":"<div><p><b>JOB SUMMARY</b></p><p>Caraway Tea is seeking Quality Assurance (QA) Manager to initially support our manufacturing facility in Highland, NY. As a QA Manager, you will be responsible for overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans. Product families include tea and herbal botanical s. This position will be responsible for ensuring products are being produced in a manner that meets all specifications and brand consistency and promoting a culture of Quality across all departments. You will also lead efforts to identify potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.</p><p><b>CORE JOB DUTIES</b>.</p><ul><li>Performs in-process and finished product sampling and inspection.</li><li>Ensures equipment and product line clearances before production runs.</li><li>Manages and writes customer complaint and product investigations, helping to assess risk, identify root cause, plan CAPA activities, and implement 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>Manage and track stability sampling and testing per state regulation.</li><li>Reviews batch manufacturing records, logbooks, test results, and ensures good documentation practices are followed.</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 GMP facility inspections.</li><li>Participates in corporate Quality internal 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), Good Agricultural Practice (GAP) and GFSI (Global Food Safety Initiative) guidance such as BRC, SQF, and FSSC 22000</li><li>Facilitates creation of and/or updates to product safety plans or product process parameters.</li><li>Overall accountability 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></ul><p><b>EQUIRED EXPERIENCE, EDUCATION AND SKILLS</b></p><ul><li>Bachelors Degree and/or Associates Degree with equivalent experience</li><li>5+ years' experience in a quality role</li><li>Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, or tobacco.</li><li>Highly desirable: FDA, HACCP, GFSI (Global Food Safety Initiative) such as BRC, SQF, and FSSC 22000</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 in 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><li>Able to manage personnel effectively, including performance issues, setting vision, priorities, etc.</li><li>Demonstrates high sense of urgency and proactive thinking</li><li>Experience with Continuous Improvement initiatives is a plus</li><li>Experience with Good Agricultural Practice (GAP) is a plus</li><li>SQF Practitioner is a bonus. But will train the right individual.</li></ul><p>Job Type: Full-time</p><p>Pay: $51,807.00 - $55,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>Dental insurance</li><li>Flexible schedule</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Day shift</li><li>Monday to Friday</li></ul><p>COVID-19 considerations:<br />Yes, we are masked and practice social distancing.</p><p>Ability to commute/relocate:</p><ul><li>Highland, NY 12528: Reliably commute or planning to relocate before starting work (Preferred)</li></ul><p>Experience:</p><ul><li>SQF: 1 year (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul><p>Work Location: One location</p></div>","company":{"name":"Caraway Tea Company LLC"},"location":{"country":"United States","address":"Highland, NY 12528","city":"Highland","stateProvince":"NY"},"frontendLink":"/job-posting/caraway-tea-company-llc/quality-control-manager/1015e3ea65f34ec1b9411231d9a62346","title":"Quality Control Manager","category":"Manufacturing","hash":"1015e3ea65f34ec1b9411231d9a62346","postingUrl":"https://www.indeed.com/job/quality-control-manager-223276d68eb6c3a1"},{"salaries":[{"salaryStart":"$49k","salaryEnd":"$81k","currency":"","source":"Salary.com","position":"Quality Assurance Specialist I","type":"per year","url":"https://www.salary.com/research/salary/benchmark/level-i-quality-assurance-specialist-salary/montreal-qc-canada"},{"salaryStart":"$39k","salaryEnd":"$70k","currency":"","source":"PayScale","position":"Quality Assurance (QA) Specialist","type":"per year","url":"https://www.payscale.com/research/CA/Job=Quality_Assurance_(QA)_Specialist/Salary/a29cb398/Montr%C3%A9al-QC"},{"salaryStart":"$60k","salaryEnd":"$65k","currency":"","source":"Glassdoor","position":"Quality Assurance Specialist","type":"per year","url":"https://www.glassdoor.ca/Salary/Equisoft-Quality-Assurance-Specialist-Montreal-Salaries-EJI_IE298587.0,8_KO9,37_IL.38,46_IM990.htm"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"9 days ago","description":"<div><p>Since the legalization of recreational Cannabis in October 2018, HEXO Corp has experienced incredible growth. As one of Canada’s top Cannabis companies, we continue to advance in this exciting new industry along with the incredibly talented people we have working on the team.</p><p>HEXO Corp creates globally trusted brands of easy-to-use and easy-to-understand cannabis products. HEXO Corp is a serious, business-oriented and socially responsible organization that is building dynamic teams of professionals that aren't afraid to step outside of their role, try new things and challenge the status quo.</p><p>If you are excited to take on a new challenge and are open to getting out of your comfort zone, we’re looking for people like you to join the HEXO Corp family.</p><p><b>Overview</b></p><p>Reporting to a Quality Manager, the Quality Specialist will be responsible for the implementation and ongoing monitoring of the quality assurance and/or quality control systems for adult use cannabis in strict compliance with Health Canada’s Cannabis regulations. The Quality Specialist is responsible for supporting the company’s Quality Management, Production, Maintenance and Facilities departments.</p><p><b>Responsibilities:</b></p><p>• Performs QA/QC monitoring for all areas of cultivation, harvest, processing and storage to ensure compliance with Health Canada’s guidelines/regulations, including GPP and GMP by working with employees of different departments on the floor;</p><p>• Performing pre-operational inspections before the start of the production, cultivation, harvest and processing activities and documenting the observations in the pre-operational inspection control sheet.</p><p>• Perform operational inspections and documenting the observations on the operational inspection control sheet.</p><p>• Performing quality inspections and quality checks at various stages of cannabis from seed to storage and report the findings in control sheet.</p><p>• Ensures compliance to process quality requirements through monitoring, documenting and collaboration with departments;</p><p>• Implement the Preventive Control Program (HACCP), Critical Control Points, verification and corrective action procedures.</p><p>• Communicates non-compliances to respective department stakeholders in a timely fashion;</p><p>• Assists the production team with QA/QC activities relative to their area;</p><p>• Performs laboratory functions such as filling the COC sheets, coordinating sampling of product, reception of the results and data entry of the lab results, and external testing, equipment management and test product development;</p><p>• Provides support for inspection/testing/analysis of raw materials;</p><p>• Participates in the investigation of problems or failures within the overall quality system, including root cause analysis, identifying corrective actions, ensuring corrective actions are completed and documenting deviations;</p><p>• As needed, supports document change control, complaints investigation and recall investigation;</p><p>• Liaises closely with colleagues and provides required QA/QC training/coaching for all areas of the facility;</p><p>• Monitors process control and QC data trends, reporting findings to quality team leads;</p><p>• Follows procedures efficiently and consistently in laboratory and production environment.</p><p>• Supports creation of Quality Assurance/Control Reports for management.</p><p>• Assists quality assurance/control requirements for production R&amp;D projects if needed.</p><p><b>Requirements:</b></p><p>• Post-secondary diploma or certificate in a technical discipline (e.g. Food, Physical, or Biological Sciences) required;</p><p>• Experience in Quality assurance in food, Pharma or cannabis industries;</p><p>• Experience in implementation of the HACCP, GFSI, FSEP</p><p>• Bilingual an asset;</p><p>• Familiarity with Health Canada Cannabis Regulations is an asset;</p><p>• Proven ability to effectively use Microsoft Office Applications;</p><p>• Detail oriented, self-directed in execution of tasks, strong critical thinking and leadership skills;</p><p>• Communication, Conflict Management, documentation and record keeping skills are an asset;</p><p>• Motivated team player with strong communication skills, attention to detail and a willingness to learn;</p><p>HEXO cultivates an inclusive and respectful workplace. This includes treating everyone with dignity and fairness, and maintaining a workplace that is free of harassment, discrimination, and violence. We welcome and encourage applications from people with disabilities and people from different backgrounds and capabilities. This diversity brings our organization a wealth of experience that builds a better team. Accommodations are available on request for candidates taking part in all aspects of the hiring and selection process</p></div>","company":{"website":"hexocorp.com","companyType":"Public/Established","name":"HEXO Operations Inc.","logoUrl":"/logos/hexo-corporation-cfa61f882259ac7f742a01266b314a98.jpeg"},"location":{"country":"Canada","address":"Gatineau, QC","city":"Gatineau","stateProvince":"QC"},"frontendLink":"/job-posting/hexo-operations-inc/quality-assurance-specialist/91672ad084096f659f5f287c373e5688","title":"Quality Assurance Specialist","category":"Medical & Healthcare","hash":"91672ad084096f659f5f287c373e5688","postingUrl":"https://www.glassdoor.ca/job-listing/quality-assurance-specialist-hexo-operations-JV_IC2301146_KO0,28_KE29,44.htm?jl=4119186713","salary":"$49k - $81k"},{"salaries":[{"salaryStart":"$120k","salaryEnd":"$130k","currency":"US","source":"Glassdoor","position":"Quality Assurance Manager","type":"per year","url":"https://www.glassdoor.co.in/Salary/General-Motors-GM-Quality-Assurance-Manager-Lansing-Salaries-EJI_IE279.0,17_KO18,43_IL.44,51_IM472.htm"},{"salaryStart":"$68k","salaryEnd":"$100k","currency":"US","source":"Monster","position":"Quality Assurance Manager","type":"per year","url":"https://www.monster.com/salary/q-quality-assurance-manager-l-east-lansing-mi"},{"salaryStart":"$91k","salaryEnd":"$150k","currency":"US","source":"Salary.com","position":"Quality Assurance Manager","type":"per year","url":"https://www.salary.com/research/salary/benchmark/quality-assurance-manager-salary/mi"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"11 days ago","description":"<div><p>AWH is a vertically integrated cannabis cultivator, processor and dispensary operator with assets in Illinois, Massachusetts Michigan and Ohio. We seek to foster a robust and inclusive cannabis organization through providing a premium, unmatched customer-focused retail experience and producing quality and mindfully created cannabis products. Our goal is to build a world class team that will continue our mission of helping to shape the future of cannabis and bettering our customers life with cannabis. How will we achieve this? By offering unrivaled quality, consistency and meticulously curated products that satisfy our customers unique, individual needs.</p><p>When it comes to customer service experience, our dispensaries will set a new standard of excellence, emphasizing health and wellness. As a team that is committed to our values, our people and our communities; we are looking for people who are inspired by our vision and stay dedicated to our mission as we scale continuously.</p><p>• *Why AWH**?</p><p>Our people are our greatest asset. Our teams are comprised of a group of skilled and passionate professionals and partners from a diverse range of fields. We believe in not only building a diverse team but creating a space where ALL feel welcome and training our leaders to not only be inclusive themselves but to inspire their teams to be the same. We provide equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, gender identity, national origin, age or disability. We believe in providing competitive compensation, quality benefits and a work environment that fosters creativity, hard work and leverage every one of our employees' unique skills while giving them what it takes to advance those said skills and learn new ones. We sweat the details to ensure our teams are confident and excited to provide best in class service to our customers and communities we serve.</p><p>The Quality Assurance Manager is responsible for monitoring and evaluating internal production processes, overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans. The Quality Assurance Manager responsible for ensuring products are being produced in a manner that meets all specifications and brand consistency and promoting a culture of Quality across all departments. The Quality Assurance Manager reports directly to the site leader.</p><p>• *Essential Duties and Responsibilities**</p><p>• Monitoring and evaluating internal production processes.</p><p>• Responsible for developing product quality safety and sanitation programs for the cultivation site.</p><p>• Build a documented consumer complaint process complete with trending, weekly reviews and trend reduction.</p><p>• Create guidance in regulations consistent with FSMA, CGMP and food CFR requirements.</p><p>• Assurance of sound raw and FG traceability program.</p><p>• Development of Master Sanitation program.</p><p>• Implementation of thorough line quality measurement systems.</p><p>• Documentation and control of all processes.</p><p>• Lead a strong pest control program.</p><p>• Developing quality control processes and design product specifications.</p><p>• Supervising staff and monitoring production standards.</p><p>• Examining the quality of raw\\/pack materials that are used in production.</p><p>• Evaluating the final output of products to determine their quality.</p><p>• Producing statistical reports on quality standards.</p><p>• Rejecting products that fail quality standards.</p><p>• Implement HACCP program all within the food work streams.</p><p>• *Supervisory Responsibilities**</p><p>• This position has no supervisory responsibilities at this time but will require engagement and accountability by managers involved in the daily operations of the facility.</p><p>• *Competencies**</p><p>• Treat people with respect, keeps commitments, inspires the trust of others, works with integrity and ethically, upholds organizational values.</p><p>• Is consistently at work and on time, ensures work responsibilities are covered when absent, arrives at meetings and appointments on time.</p><p>• Observes and adheres to regulatory, safety and security procedures.</p><p>• Ability to maintain a 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-driven environment while successfully managing multiple tasks.</p><p>• *Requirements and Qualifications**</p><p>• 2 year degree in Business Administration, or relevant field. 4 year degree preferred.</p><p>• Quality Control Certification preferred.</p><p>• Minimum 3 – 5 years as a Site Quality Manager; strong food experience is a plus</p><p>• Ability to build and manage external auditing such as SQF or BRC initiatives.</p><p>• Lean manufacturing experience and HACCP certified a plus.</p><p>• Advanced CAPA, RCA, and strategic planning experience</p><p>• Advanced experience conducting audits, data analysis and reporting statistics.</p><p>• Highly computer literate and proficient in MS Office including Excel, PowerPoint, Word and data analytics.</p><p>• Excellent critical thinking and problem-solving skills.</p><p>• Excellent interpersonal and communication skills including speaking and writing.</p><p>• Proven track record in people leadership (supporting, developing, engaging) with demonstrated teambuilding and collaboration skills.</p><p>• Must\\u200B \\u200Bbe\\u200B \\u200Ba\\u200Bt least \\u200B21\\u200B \\u200Byears\\u200B \\u200Bof\\u200B \\u200Bage.</p><p>• Must\\u200B \\u200Bpass\\u200B \\u200Bany\\u200B \\u200Band\\u200B \\u200Ball\\u200B \\u200Brequired\\u200B \\u200Bbackground\\u200B \\u200Bchecks.</p><p>• Must\\u200B \\u200Bbe\\u200B \\u200Band\\u200B \\u200Bremain\\u200B \\u200Bcompliant\\u200B \\u200Bwith\\u200B \\u200Bany\\u200B \\u200Band\\u200B \\u200Ball\\u200B \\u200Bregulatory requirements\\u200B \\u200Bfor\\u200B \\u200Bworking\\u200B \\u200Bin\\u200B \\u200Bthe cannabis industry.</p><p>• Must\\u200B be able to \\u200Bobtain\\u200B \\u200Band\\u200B \\u200Bretain\\u200B \\u200Ba\\u200B \\u200BRegistered Agent Card issued by the MA Cannabis Control Commission.</p><p>• Must have excellent organization and time management skills.</p><p>• Must be focused, pay close attention to detail and accuracy of data recorded.</p><p>• Must be able to internalize training and \\u200Bfollow instructions consistently.</p><p>• Must be able to work effectively as part of a team and grow with the company</p><p>• *Work Environment**</p><p>This position performs duties in an agricultural\\/manufacturing environment.</p><p>• *EEO STATEMENT:**</p><p>Ascend Wellness Holdings, LLC and its subsidiaries is an equal opportunity employer and celebrate the population of differences, and does not discriminate in its hiring \\/ hiring practices, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status or any other characteristic protected by law.</p><p>Location: Lansing, Michigan, United States</p><p><b>Skills required for this job:</b></p><p>• Customer service</p></div>","company":{"companyType":"Private/Established","name":"AWH","logoUrl":"/logos/awh-4fde58360265383fe2c8cebe7c77e375.png"},"location":{"country":"United States","address":"Lansing, MI, USA","city":"Lansing","stateProvince":"MI"},"frontendLink":"/job-posting/awh/quality-assurance-manager/4bd56e7841f220b95060c115bc3d3749","title":"Quality Assurance Manager","category":"Information Technology & Services","hash":"4bd56e7841f220b95060c115bc3d3749","postingUrl":"https://torre.co/jobs/JWO9Aqod-awh-quality-assurance-manager-2","salary":"$120k - $130k"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"2 days ago","description":"<div><p>Quality Assurance Associate - Processing Leamington ON.</p><p>Monday-Friday 11:00PM-7:30AM</p><p>About Tilray</p><p>Tilray is a global pioneer in cannabis research, cultivation, processing and distribution currently serving tens of thousands of patients in ten countries spanning five continents.</p><p>Looking to develop your career at the forefront of a rapidly expanding industry?</p><p><b>Job Summary:</b></p><p>Reporting to the Quality Assurance Supervisor, this position will be responsible for supporting Tilray's Quality Assurance team in the cultivation department. As industry leaders committed to offering clean, safe, and pure cannabis products, we engage in a collaborative culture that is fast paced, dynamic and highly motivating. If you’re looking to thrive in a new, rapidly growing and innovative space, we would love to hear from you. We are currently seeking a strong leader to join our Quality team. This position will be Monday-Friday with some required Saturdays on a rotational swing shift of 6:30AM-3:00PM 3:00PM-11:30PM.</p><p><b>Your day-to-day responsibilities will consist of:</b></p><p>• Continually monitor processing areas for GPP regulatory requirements under the Cannabis Act and Cannabis Regulations and their associated regulations such as those for Natural Health Products.</p><p>• Assist all functional departments on establishing systems to eliminate GACP/GPP gaps that relate to Processing and manufacturing</p><p>• Support and maintain systems to ensure quality of products as defined through internal Good Production Practices and established Standard Operating Procedures.</p><p>• Communicate, educate and support the quality requirements to all operational departments.</p><p>• Create, review and maintain Standard Operational Procedures, investigate non-conformances/deviations and customer complaints as it relates to quality.</p><p>• Participate in the initiation and writing of change controls to controlled documents as needed to ensure defined quality objectives are met</p><p>• Coordinate and conduct new hire and ongoing GPP/GACP training.</p><p>• Read, understand and follow safe work procedures</p><p>• Other duties as assigned</p><p><b>To be successful in this position you will have the following:</b></p><p>• A combination of bachelor’s degree in science related field and/or technical Diploma from an accredited post-secondary institution.</p><p>• Quality experience in a horticulture, food or health product environment is preferred</p><p>• Knowledge of plant science, pest management, GPP/GACP (Good Production Practices/Good Agricultural and Collection Practices) or GMP (Good manufacturing Practices) would be considered an asset</p><p>• Superior communication and writing skills</p><p>• Self-starter, critical thinker and team oriented</p><p>• High work ethic standards are a must</p><p>• Exceptional attention to detail</p><p>• Candidates must be able to work swing shift hours (two weeks days 6:30 am-3:00 pm, two weeks afternoons 8:30am-5:00pm). Weekend coverage may be required.</p><p>• Due to the nature of the business and working with controlled substances, all new employees will be required to complete a background check prior to starting work. This may include: verifying work references, validating all credentials and criminal record checks.</p><p>• It is a requirement that the selected Candidate be legally eligible to work in Canada at the time an offer is presented.</p><p>Internal Candidates: For any internal applicants, we ask that you bring a hard copy of your resume with a supporting cover letter to the Human Resources Office, send a direct email to our Talent Acquisition Specialist or apply online at https://www.tilray.com/careers</p><p>Note: The statements above are intended to describe the general nature and level of work being performed by people assigned to the job. They are not constructed to be an exhaustive list of responsibilities, duties and skills required of personnel in the job. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer. Tilray is committed to providing an accessible and barrier-free environment. Please advise Human Resources if you require accommodation during any part of the recruitment process</p></div>","company":{"website":"tilray.com","companyType":"Public/Established","name":"Tilray","logoUrl":"/logos/tilray-7a827f507c4afad3caee3c003054401d.png"},"location":{"country":"Canada","address":"Leamington, ON","city":"Leamington","stateProvince":"ON"},"frontendLink":"/job-posting/tilray/quality-assurance-associate-midnights/8142efbc942057795fa065651affcd6a","title":"Quality Assurance Associate (Midnights)","category":"Medical & Healthcare","hash":"8142efbc942057795fa065651affcd6a","postingUrl":"https://www.ziprecruiter.com/c/Tilray/Job/Quality-Assurance-Associate-(Midnights)/-in-Leamington,ON?jid=ec33ec97b92a3af3"},{"employmentType":"Contractor","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"2 days ago","description":"<div><p>Quality Assurance Associate - Processing Leamington ON.</p><p>Monday-Friday 11:00PM-7:30AM</p><p>About Tilray</p><p>Tilray is a global pioneer in cannabis research, cultivation, processing and distribution currently serving tens of thousands of patients in ten countries spanning five continents.</p><p>Looking to develop your career at the forefront of a rapidly expanding industry?</p><p><b>Job Summary</b></p><p>Reporting to the Quality Assurance Supervisor, this position will be responsible for supporting Tilray's Quality Assurance team in the cultivation department. As industry leaders committed to offering clean, safe, and pure cannabis products, we engage in a collaborative culture that is fast paced, dynamic and highly motivating. If you’re looking to thrive in a new, rapidly growing and innovative space, we would love to hear from you. We are currently seeking a strong leader to join our Quality team. This position will be Monday-Friday with some required Saturdays on a rotational swing shift of 6:30AM-3:00PM 3:00PM-11:30PM.</p><p>Your Day-to-day Responsibilities Will Consist Of</p><p>• Continually monitor processing areas for GPP regulatory requirements under the Cannabis Act and Cannabis Regulations and their associated regulations such as those for Natural Health Products.</p><p>• Assist all functional departments on establishing systems to eliminate GACP/GPP gaps that relate to Processing and manufacturing</p><p>• Support and maintain systems to ensure quality of products as defined through internal Good Production Practices and established Standard Operating Procedures.</p><p>• Communicate, educate and support the quality requirements to all operational departments.</p><p>• Create, review and maintain Standard Operational Procedures, investigate non-conformances/deviations and customer complaints as it relates to quality.</p><p>• Participate in the initiation and writing of change controls to controlled documents as needed to ensure defined quality objectives are met</p><p>• Coordinate and conduct new hire and ongoing GPP/GACP training.</p><p>• Read, understand and follow safe work procedures</p><p>• Other duties as assigned</p><p><b>To be successful in this position you will have the following:</b></p><p>• A combination of bachelor’s degree in science related field and/or technical Diploma from an accredited post-secondary institution.</p><p>• Quality experience in a horticulture, food or health product environment is preferred</p><p>• Knowledge of plant science, pest management, GPP/GACP (Good Production Practices/Good Agricultural and Collection Practices) or GMP (Good manufacturing Practices) would be considered an asset</p><p>• Superior communication and writing skills</p><p>• Self-starter, critical thinker and team oriented</p><p>• High work ethic standards are a must</p><p>• Exceptional attention to detail</p><p>• Candidates must be able to work swing shift hours (two weeks days 6:30 am-3:00 pm, two weeks afternoons 8:30am-5:00pm). Weekend coverage may be required.</p><p>• Due to the nature of the business and working with controlled substances, all new employees will be required to complete a background check prior to starting work. This may include: verifying work references, validating all credentials and criminal record checks.</p><p>• It is a requirement that the selected Candidate be legally eligible to work in Canada at the time an offer is presented.</p><p>Internal Candidates: For any internal applicants, we ask that you bring a hard copy of your resume with a supporting cover letter to the Human Resources Office, send a direct email to our Talent Acquisition Specialist or apply online at https://www.tilray.com/careers</p><p>Note: The statements above are intended to describe the general nature and level of work being performed by people assigned to the job. They are not constructed to be an exhaustive list of responsibilities, duties and skills required of personnel in the job. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer. Tilray is committed to providing an accessible and barrier-free environment. Please advise Human Resources if you require accommodation during any part of the recruitment process</p></div>","company":{"website":"tilray.com","companyType":"Public/Established","name":"Tilray","logoUrl":"/logos/tilray-7a827f507c4afad3caee3c003054401d.png"},"location":{"country":"Canada","address":"Staples, ON","city":"Staples","stateProvince":"ON"},"frontendLink":"/job-posting/tilray/quality-assurance-associate-midnights/732dde43e13843fde509843580486f38","title":"Quality Assurance Associate (Midnights)","category":"Medical & Healthcare","hash":"732dde43e13843fde509843580486f38","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-associate-midnights-at-tilray-2766129149"},{"salaries":[{"salaryStart":"$58k","salaryEnd":"$100k","currency":"US","source":"Salary.com","position":"Quality Control Supervisor I","type":"per year","url":"https://www.salary.com/research/salary/benchmark/quality-control-supervisor-i-salary/denver-co"},{"salaryStart":"$71k","salaryEnd":"$110k","currency":"US","source":"ZipRecruiter","position":"Construction Quality Control Manager","type":"per year","url":"https://www.ziprecruiter.com/Salaries/Construction-Quality-Control-Manager-Salary-in-Denver,CO"},{"salaryStart":"$58k","salaryEnd":"$100k","currency":"US","source":"PayScale","position":"Quality Manager","type":"per year","url":"https://www.payscale.com/research/US/Job=Quality_Manager/Salary/8dbfb511/Denver-CO-Quality-Assurance-Quality-Control"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"15 days ago","description":"<div><p><b>The Company</b></p><p>At Canopy Growth, our mission is clear: improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We're building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.</p><p>With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.</p><p>Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!</p><p><b>The Opportunity</b></p><p>This role will be responsible for supporting the QA CMO Manager in developing, implementing, and enforcing quality standards, policies, procedures, and programs to ensure safe and compliant production with our contract manufacturers. You will also assist with efforts to track and trend data, identify potential quality risks and work cross functionally to support improvement opportunities.</p><p><b>Responsibilities</b></p><p>• Work with multiple third-party labs/sites/manufacturers to gather and provide batch release documentation, including COA's for products manufactured or processed on-site or off-site, and escalate any delays or issues to management</p><p>• Perform batch specific quality inspections in ERP system to release contract manufactured goods for sale</p><p>• Create and maintain quality inspection parameters in ERP system for all products and ensure expiry management processes are in place and functioning</p><p>• Maintain API traceability in ERP system from farm to extraction to production to sales.</p><p>• Collect and coordinate the sampling and testing of API and contract manufactured products as necessary to ensure compliance</p><p>• Provide correspondence to production planning and logistics with regards to requests for release documentation and batch status updates</p><p>• Perform analysis of reports and production data to identify trends &amp; areas of improvement; make recommendation on continuous improvement projects</p><p>• Draft Quality and other operational procedures, policies, forms, work instructions etc. and ensure compliance to document management processes</p><p>• Participate in the investigation of non-conformances, corrective action &amp; monitoring closure, determine inefficiencies, and streamline processes</p><p>• Support operations in third party audits, self-assessments, and process risk assessments to comply with requirements and continued compliance</p><p>• Other duties as assigned</p><p><b>Experience</b></p><p>• Bachelor's Degree</p><p>• 5+ years of demonstrated technical leadership and organization/control skills</p><p>• Must have excellent communication skills and be able to work in a fast - paced environment with conflicting priorities</p><p>• Must have excellent computer skills and experience with Microsoft Office Word, Excel and Adobe</p><p>• SAP experience a plus</p><p>• Data analytics is a plus</p><p>• Process oriented</p><p>• Strong business acumen, and strategic thinking</p><p>• Continuous Improvement experience would be an asset</p><p><b>Other Details</b></p><p>This is a full-time position based out of Denver, CO.</p><p>Canopy Growth offers a wide range of benefits for employees in the United States including: medical, dental, vision, life insurance, short-term disability, long-term disability, 401k plan, and paid time off.</p><p>Pay range: $82,000 USD per year, commensurate with experience, specific to Colorado.</p><p>We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don't hear from us, don't fret; every resume we get is kept in our database for six months for consideration in future searches for talent.</p><p>Canopy Growth welcomes and encourages applications from people with disabilities.</p><p>Accommodations are available upon request for candidates taking part in all aspects of the selection process.</p><p>One last note: the chosen applicant will be required to successfully complete background and reference checks.</p><p>Thank you so much for your interest in Canopy Growth.</p><p>Apply Now</p><p>• Denver, CO, USA</p></div>","company":{"website":"canopygrowth.com","companyType":"Public/Established","name":"Canopy Growth Corp.","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"United States","address":"Denver, CO, USA","city":"Denver","stateProvince":"CO"},"frontendLink":"/job-posting/canopy-growth-corp/supervisor-quality-control/9201d1f3009d4be72f301652ec027e10","title":"Supervisor, Quality Control","category":"Medical & Healthcare","hash":"9201d1f3009d4be72f301652ec027e10","postingUrl":"https://www.apply4itjobs.com/job-in-Denver-Colorado-USA/SUPERVISOR-QUALITY-CONTROL-0f5576dad90db96700/v2/","salary":"$58k - $100k"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"12 days ago","description":"<div>The Company<br /><b>At Canopy Growth, our mission is clear:</b> improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We’re building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.<br />With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.<br />Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!<br /><br />The Opportunity<br /><br />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.<br /><br />Responsibilities<br /><ul><li>Author test cases and test plans for new and existing web site features</li><li>Test functional changes being made for new features, feature enhancements, and bug fixes</li><li>Cross browser and device combability testing</li><li>Write Python or Java code to automate Selenium testing</li><li>Work with the application services and infrastructure teams to select and deploy testing platforms and frameworks</li><li>Assist developers monitor APM and fault logging facilities to proactively evaluate application performance</li><li>Help standardize testing environments to better reflect production environments</li></ul>Experience<br /><ul><li>2+ years of experience writing test cases and test plans in a TCM (Test Case Management) application (e.g. Test Rail)</li><li>2+ year of experience with frontend technologies (HTML, Javascript, VueJS or others)</li><li>Prior experience with e-commerce web sites</li><li>Experience coding in Python or Java</li><li>Experience with frontend testing frameworks (Selenium, Katalon Studio or others)</li><li>Experience with software development project tools (Git, Jira)</li><li>Experience with Bugsnag and Datadog or equivalent tools an asset</li><li>Good verbal and communication skills</li><li>Academic degree or comparable education and work experience</li></ul>Other Details<br />This is a full-time role based out of Kanata, Toronto, or Montreal.<br /><br />We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don’t hear from us, don’t fret; every resume we get is kept in our database for six months for consideration in future searches for talent.<br />Canopy Growth welcomes and encourages applications from people with disabilities.<br />Accommodations are available upon request for candidates taking part in all aspects of the selection process.<br /><b>One last note:</b> the chosen applicant will be required to successfully complete background and reference checks.<br />Thank you so much for your interest in Canopy Growth.</div>","company":{"companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Toronto, ON","city":"Toronto","stateProvince":"ON"},"frontendLink":"/job-posting/canopy-growth-corporation/web-quality-assurance/4ce29129935945e031938b82ea631f42","title":"Web Quality Assurance","category":"Medical & Healthcare","hash":"4ce29129935945e031938b82ea631f42","postingUrl":"https://ca.indeed.com/job/web-quality-assurance-c87fb44e929f584a"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"12 days ago","description":"<div><p><b>The Company</b></p><p>At Canopy Growth, our mission is clear: improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We’re building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.</p><p>With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.</p><p>Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!</p><p><b>The Opportunity</b></p><p>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.</p><p><b>Responsibilities</b></p><p>• Author test cases and test plans for new and existing web site features</p><p>• Test functional changes being made for new features, feature enhancements, and bug fixes</p><p>• Cross browser and device combability testing</p><p>• Write Python or Java code to automate Selenium testing</p><p>• Work with the application services and infrastructure teams to select and deploy testing platforms and frameworks</p><p>• Assist developers monitor APM and fault logging facilities to proactively evaluate application performance</p><p>• Help standardize testing environments to better reflect production environments</p><p><b>Experience</b></p><p>• 2+ years of experience writing test cases and test plans in a TCM (Test Case Management) application (e.g. Test Rail)</p><p>• 2+ year of experience with frontend technologies (HTML, Javascript, VueJS or others)</p><p>• Prior experience with e-commerce web sites</p><p>• Experience coding in Python or Java</p><p>• Experience with frontend testing frameworks (Selenium, Katalon Studio or others)</p><p>• Experience with software development project tools (Git, Jira)</p><p>• Experience with Bugsnag and Datadog or equivalent tools an asset</p><p>• Good verbal and communication skills</p><p>• Academic degree or comparable education and work experience</p><p><b>Other Details</b></p><p>This is a full-time role based out of Kanata, Toronto, or Montreal.</p><p>We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don’t hear from us, don’t fret; every resume we get is kept in our database for six months for consideration in future searches for talent.</p><p>Canopy Growth welcomes and encourages applications from people with disabilities.</p><p>Accommodations are available upon request for candidates taking part in all aspects of the selection process.</p><p>One last note: the chosen applicant will be required to successfully complete background and reference checks.</p><p>Thank you so much for your interest in Canopy Growth</p></div>","company":{"website":"canopygrowth.com","companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/canopy-growth-corporation/web-quality-assurance/3db4a17078fe4f9b3cf4f0df805b8c4d","title":"Web Quality Assurance","category":"Medical & Healthcare","hash":"3db4a17078fe4f9b3cf4f0df805b8c4d","postingUrl":"https://jobs.laimoon.com/jobs/externalview/28671661"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"12 days ago","description":"<div>The Company<br /><b>At Canopy Growth, our mission is clear:</b> improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We’re building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.<br />With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.<br />Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!<br /><br />The Opportunity<br /><br />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.<br /><br />Responsibilities<br /><ul><li>Author test cases and test plans for new and existing web site features</li><li>Test functional changes being made for new features, feature enhancements, and bug fixes</li><li>Cross browser and device combability testing</li><li>Write Python or Java code to automate Selenium testing</li><li>Work with the application services and infrastructure teams to select and deploy testing platforms and frameworks</li><li>Assist developers monitor APM and fault logging facilities to proactively evaluate application performance</li><li>Help standardize testing environments to better reflect production environments</li></ul>Experience<br /><ul><li>2+ years of experience writing test cases and test plans in a TCM (Test Case Management) application (e.g. Test Rail)</li><li>2+ year of experience with frontend technologies (HTML, Javascript, VueJS or others)</li><li>Prior experience with e-commerce web sites</li><li>Experience coding in Python or Java</li><li>Experience with frontend testing frameworks (Selenium, Katalon Studio or others)</li><li>Experience with software development project tools (Git, Jira)</li><li>Experience with Bugsnag and Datadog or equivalent tools an asset</li><li>Good verbal and communication skills</li><li>Academic degree or comparable education and work experience</li></ul>Other Details<br />This is a full-time role based out of Kanata, Toronto, or Montreal.<br /><br />We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don’t hear from us, don’t fret; every resume we get is kept in our database for six months for consideration in future searches for talent.<br />Canopy Growth welcomes and encourages applications from people with disabilities.<br />Accommodations are available upon request for candidates taking part in all aspects of the selection process.<br /><b>One last note:</b> the chosen applicant will be required to successfully complete background and reference checks.<br />Thank you so much for your interest in Canopy Growth.</div>","company":{"companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Ottawa, ON","city":"Ottawa","stateProvince":"ON"},"frontendLink":"/job-posting/canopy-growth-corporation/web-quality-assurance/19e82ee3547862be5c6108ed0b82683c","title":"Web Quality Assurance","category":"Medical & Healthcare","hash":"19e82ee3547862be5c6108ed0b82683c","postingUrl":"https://ca.indeed.com/job/web-quality-assurance-091ad0078f9a05a2"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"12 days ago","description":"<div>The Company<br /><b>At Canopy Growth, our mission is clear:</b> improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We’re building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.<br />With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.<br />Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!<br /><br />The Opportunity<br /><br />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.<br /><br />Responsibilities<br /><ul><li>Author test cases and test plans for new and existing web site features</li><li>Test functional changes being made for new features, feature enhancements, and bug fixes</li><li>Cross browser and device combability testing</li><li>Write Python or Java code to automate Selenium testing</li><li>Work with the application services and infrastructure teams to select and deploy testing platforms and frameworks</li><li>Assist developers monitor APM and fault logging facilities to proactively evaluate application performance</li><li>Help standardize testing environments to better reflect production environments</li></ul>Experience<br /><ul><li>2+ years of experience writing test cases and test plans in a TCM (Test Case Management) application (e.g. Test Rail)</li><li>2+ year of experience with frontend technologies (HTML, Javascript, VueJS or others)</li><li>Prior experience with e-commerce web sites</li><li>Experience coding in Python or Java</li><li>Experience with frontend testing frameworks (Selenium, Katalon Studio or others)</li><li>Experience with software development project tools (Git, Jira)</li><li>Experience with Bugsnag and Datadog or equivalent tools an asset</li><li>Good verbal and communication skills</li><li>Academic degree or comparable education and work experience</li></ul>Other Details<br />This is a full-time role based out of Kanata, Toronto, or Montreal.<br /><br />We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don’t hear from us, don’t fret; every resume we get is kept in our database for six months for consideration in future searches for talent.<br />Canopy Growth welcomes and encourages applications from people with disabilities.<br />Accommodations are available upon request for candidates taking part in all aspects of the selection process.<br /><b>One last note:</b> the chosen applicant will be required to successfully complete background and reference checks.<br />Thank you so much for your interest in Canopy Growth.</div>","company":{"companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Montréal, QC","city":"MontréAl","stateProvince":"QC"},"frontendLink":"/job-posting/canopy-growth-corporation/web-quality-assurance/4e8743ddc2ed019f4cad1fe9bd540e83","title":"Web Quality Assurance","category":"Medical & Healthcare","hash":"4e8743ddc2ed019f4cad1fe9bd540e83","postingUrl":"https://ca.indeed.com/job/web-quality-assurance-4a93fdc05167faa7"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"13 days ago","description":"<div><p><b>Quality Assurance Manager/QAP</b></p><p>Our client is searching for a for a talented and ambitious Quality Assurance Person/Manager who will be responsible for building and managing the Quality Assurance team. You will maintain and build upon the company’s quality management program to implement quality processes, systems, and relationships and drive best in class quality and performance.</p><p>You will act as the primary Quality Assurance Person (QAP) on the license, overseeing testing, review, and release of all products entering the market.</p><p>The Quality assurance manager/QAP is accountable for the development, implementation and ongoing monitoring of the quality assurance and control systems in strict compliance with The Cannabis Act. The QAP is responsible for representing the company’s QA/QC Department in all reports in relations to Health Canada.</p><p><b>Role and Responsibilities: </b></p><p>· Act as the primary QAP on the site license(s), as designated by Health Canada</p><p>· Draft and approve all Standard Operating Procedures (SOPs) for site activities</p><p>· Maintain all technical documents pertaining to Standard Operating Procedures</p><p>· Establish and enforce GAP, GPP, GMP, GLP and HACCP and quality assurance standards, providing technical and regulatory input for growing, packaging, and production</p><p>· Review and approve all packaging and labeling for compliance with Cannabis Regulations</p><p>· Review and approve all third-party analytical test results against established specifications</p><p>· Maintain standards of quality and GPP/GMP compliance through training and mentorship within and outside of the department, staff development, monitoring performance of the quality systems</p><p>· Ensure compliance with Health Canada’s QA guidelines pertaining to business, production, facility, security, storage, packaging, and labeling for the Cannabis Act</p><p>· Support the facility on all scheduled and unplanned inspections by a regulator</p><p>· Monitoring and reporting of quality systems metrics to drive performance and identify trends for action and implements quality assurance systems</p><p>· Ensure that destruction is managed and compliant with SOPs and the Cannabis Act</p><p>· Coordinate all key product quality issues such as complaint handling, recall coordination, investigations on deviations/failures and implementing corrective and preventive actions (CAPA)</p><p>· Review status of process materials and ensure proper control, release and transfer of materials for production and sale through proper documentation and/or ERP System</p><p>· Ensure Corrective Action and Preventative Action (CAPA) investigations are conducted appropriately and closed in a timely manner</p><p>· Oversee an effective sanitation program to ensure production, packaging, labeling and storage activities are conducted under sanitary conditions</p><p>· Coordinate external testing of materials/products and perform in-house testing of stating materials, bulk and finished product as per approved specifications</p><p>· Train staff in SOPs to ensure the correct implementation in operations and regulatory compliance</p><p>· Review testing raw data, analytical reports, and Certificate of Analysis (CoA) of each product batch prior to its release for sale</p><p>· Support continuous quality improvement through reinforcement of product quality and safety programs, sanitization program and oversight of security system</p><p>· Develop the QA budget for review</p><p><b>Education and Experience.</b></p><ul><li>Bachelor’s degree in a technical discipline (Food, Physical, or Biological Sciences preferred) is required;</li><li>3+ years of experience as a Quality Assurance Manager in a GAP, GPP, GMP, GLP and HACCP regulated environment, with proficiency in quality assurance systems, documentation, and testing methods</li><li>Strong and current knowledge of the Cannabis Act &amp; Regulations, Good Production Practice, Good Agricultural Practice, Good Manufacturing Practice, Good Laboratory Practice, HACCP, Food Safety, and environmental guidelines</li><li>Ability to review regulations, documents, and reports pertaining to Non-Conforming Reports (NCR), Corrective Action Reports (CR), Food &amp; Drugs Act (FDA), Controlled Drugs &amp; Substances Act (CDSA), and Pest Control Act (PCPA)</li><li>Experience in identifying GPP gaps with experience in writing SOPS, work instructions, HACCP plans, and identifying omissions within regulatory requirements</li><li>Strong quality decision making skills; with an understanding of root cause analysis and ability to lead and support critical investigations</li></ul><p><b>Requirements: </b></p><ul><li>Possess strong leadership, motivational, and mentorship experience and skills</li><li>Be highly personable, entrepreneurial, team oriented, and collaborative</li><li>Possess strong communication skills both written and verbal,</li><li>Security Clearance Holder status and QAP designation is a strong asset</li><li>Proficient in MS Office Suite software (Excel, Outlook, Word)</li><li>The Cannabis Act requires candidates to undergo security/background checks, and the individual must be approved by Health Canada as suitable for the QAP role.</li><li>Must be legally eligible to work in Canada</li></ul><p>Our Client cultivates an inclusive and respectful workplace. This includes treating everyone with dignity and fairness, and maintaining a workplace that is free of harassment, discrimination, and violence. We welcome and encourage applications from people with disabilities and people from different backgrounds and capabilities.</p><p>Job Type: Full-time</p><p>Salary: $46,176.00-$104,641.00 per year</p><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Education:</p><ul><li>Bachelor's Degree (required)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 3 years (required)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Startup","name":"2Kfinishers Inc."},"location":{"country":"Canada","address":"Montréal, QC","city":"MontréAl","stateProvince":"QC"},"frontendLink":"/job-posting/2kfinishers-inc/quality-assurance-manager-qap/4d658ac2789901b25f5d4e7311c9cb5a","title":"Quality Assurance Manager/QAP","category":"Supply Chain & Logistics","hash":"4d658ac2789901b25f5d4e7311c9cb5a","postingUrl":"https://ca.indeed.com/job/quality-assurance-managerqap-04f0132402285527"},{"function":["Quality Assurance & Regulatory Affairs"],"postedOn":"13 days ago","description":"<div><div><p><b><i>Who we are</i></b></p><p>Here at Vireo Health, Inc. ( Vireo ) our mission is to bring the best of technology, science, and engineering to the cannabis industry. We are a physician-led, customer-focused team of more than 500 dedicated employees creating best-in-class cannabis products and customer experiences. Vireo is proud to have one of the most diverse workforces in cannabis, promoting diversity, equity, and inclusion through engaging employee outreach programs, community events, and non-profit partnerships. We are rapidly expanding nationwide, and we are looking for talented, compassionate, and dedicated people to join our team and help us grow. From Cultivation to Operations to Sales &amp; Marketing, we are hiring people who share our vision and passion for improving people s lives. If you are looking for a positive work environment where your contributions truly make a difference, click apply and let us learn about you!</p><p><b><i>What you will do</i></b></p><p>We are seeking an experienced and energetic <b><i>Quality Assurance Specialist </i></b>to join our growing dynamic team! The ideal candidate will be driven, innovative, compassionate, believe in the goodness of people and cannabis, and enjoys the one team, one dream motto! The Quality Assurance Specialist is responsible for quality inspections of Medical Cannabis products and monitoring the processes and procedures in the medical cannabis manufacturing operation. This position will report directly to the Quality Manager.</p><p><b><i>Highlighted Responsibilities</i></b></p><ul><li>Perform Quality Control inspections on Products, Equipment and procedures. Ensure package integrity and accuracy.</li><li>May perform or assist inventory management personnel with inventory audits when needed.</li><li>Responsible for monitoring product cannabis safety and quality throughout the manufacturing process.</li><li>Ensure all cannabis and cannabis containing products produced at the facility are properly tested in accordance with company procedures and guidelines, at appropriate frequencies, and meet specifications prior to release. Ensure testing data is appropriately recorded and maintained.</li><li>Responsible for performing verification on equipment and other areas required.</li><li>Responsible for ensuring the correct recording and filing of all relevant record logs and documentation completed by staff.</li><li>Ensures the correct guidelines for production are followed during operations.</li><li>Ensures employees are following all SOPs, Work Instructions and worker safety practices.</li><li>Ensure the facility follows applicable Quality Management directives such as SOP s, manuals, policies and procedures, work instructions, etc.</li><li>Assist Quality Manager with instructing employees on Quality Improvements and Issues.</li><li>Analyze quality data to recommend quality and process improvements.</li><li>Collect product samples for Product Development, lab retains and the laboratory when directed.</li><li>Assist in aligning the company with all state, federal and 3rd party requirements. Compliance will work with QA to ensure compliance with government regulatory agencies and third-party audits.</li><li>Support QA Manager and assist other QA Specialists as needed.</li></ul><p></p><p><b><i>Qualifications</i></b></p><ul><li>21 years or older.</li><li>Experience with record keeping/internal auditing.</li><li>2+ years of experience in a manufacturing or quality control setting.</li><li>Ability to follow existing inventory/inspection procedures accurately.</li><li>Working knowledge of general computer operation and competency with Microsoft Office Products.</li><li>Experience operating in a quality-centric setting (Medical/Manufacturing/Health related industries).</li><li>Good writing/reading/arithmetic skills.</li><li>Basic physical ability to walk back and forth across facility and lift/move up to 50lbs if necessary.</li><li>Self-motivated with proven leadership skills and attention to detail.</li><li>Strong interpersonal skills for multitasking and interacting with team member.</li></ul><p><b><i>EEO Statement</i></b></p><p><i>Vireo Health, Inc. is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. </i><b><i>www.vireohealth.com</i></b></p></div><p></p></div>","company":{"companyType":"Private/Established","name":"Vireo Health Inc.","logoUrl":"/logos/vireo-health-125544955cfe8cdd68bc5cddd679f996.png"},"location":{"country":"United States","address":"Amado, AZ","city":"Amado","stateProvince":"AZ"},"frontendLink":"/job-posting/vireo-health-inc/quality-assurance-specialist/56735cf2d5efe7c3383b921a95c37ee8","title":"Quality Assurance Specialist","category":"Medical & Healthcare","hash":"56735cf2d5efe7c3383b921a95c37ee8","postingUrl":"https://www.indeed.com/job/quality-assurance-specialist-976559a662033c97"},{"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"13 days ago","description":"<div><p><b>The Company</b></p><p>At Canopy Growth, our mission is clear: improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We’re building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.</p><p>With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.</p><p>Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!</p><p><b>The Opportunity</b></p><p>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.</p><p><b>Responsibilities</b></p><p>• Author test cases and test plans for new and existing web site features</p><p>• Test functional changes being made for new features, feature enhancements, and bug fixes</p><p>• Cross browser and device combability testing</p><p>• Write Python or Java code to automate Selenium testing</p><p>• Work with the application services and infrastructure teams to select and deploy testing platforms and frameworks</p><p>• Assist developers monitor APM and fault logging facilities to proactively evaluate application performance</p><p>• Help standardize testing environments to better reflect production environments</p><p><b>Experience</b></p><p>• 2+ years of experience writing test cases and test plans in a TCM (Test Case Management) application (e.g. Test Rail)</p><p>• 2+ year of experience with frontend technologies (HTML, Javascript, VueJS or others)</p><p>• Prior experience with e-commerce web sites</p><p>• Experience coding in Python or Java</p><p>• Experience with frontend testing frameworks (Selenium, Katalon Studio or others)</p><p>• Experience with software development project tools (Git, Jira)</p><p>• Experience with Bugsnag and Datadog or equivalent tools an asset</p><p>• Good verbal and communication skills</p><p>• Academic degree or comparable education and work experience</p><p><b>Other Details</b></p><p>This is a full-time role based out of Kanata, Toronto, or Montreal.</p><p>We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don’t hear from us, don’t fret; every resume we get is kept in our database for six months for consideration in future searches for talent.</p><p>Canopy Growth welcomes and encourages applications from people with disabilities.</p><p>Accommodations are available upon request for candidates taking part in all aspects of the selection process.</p><p>One last note: the chosen applicant will be required to successfully complete background and reference checks.</p><p>Thank you so much for your interest in Canopy Growth.</p><p>Apply Now</p></div>","company":{"website":"canopygrowth.com","companyType":"Public/Established","name":"Canopy Growth Corporation","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"Canada","address":"Montreal, QC","city":"Montreal","stateProvince":"QC"},"frontendLink":"/job-posting/canopy-growth-corporation/web-quality-assurance/e91425c0e1ca913cb152e61baad9c5d8","title":"Web Quality Assurance","category":"Medical & Healthcare","hash":"e91425c0e1ca913cb152e61baad9c5d8","postingUrl":"https://ca.linkedin.com/jobs/view/web-quality-assurance-at-canopy-growth-corporation-2750467317"},{"employmentType":"Full-time, Permanent","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"14 days ago","description":"<div><p><b>Company description</b></p><p>We are a small private licensed producer with a cultivation and processing license and we are located in Kelowna, BC. We are looking for a quality assurance person who will join our dynamic team. We offer a full health benefit plan, hours of operation 7-3:30 Monday to Friday . Depending on experience, the salary range is from $80,000 - $90,000 yearly.</p><p><b>Job description</b></p><p>Quality Assurance Person for Oakum Cannabis Corp, Kelowna, BC</p><p>Under the direction and the supervision of the CEO, the Quality Assurance Person ensures that quality standards and current procedures meet or exceed Canadian Cannabis regulations for Good Production Practices as well as the standards set out by the Cannabis Act, Health Canada.</p><p>Duties include writing, reviewing and implementing consistent quality standards, goals and objectives in conjunction with designated management and leading the development and standardization of quality specific policies and procedures, continuing education and training programs.</p><p>The Quality Assurance Person is responsible for tracking, monitoring and reporting on quality, and safety initiatives, quality indicators and laboratory occurrences. Monitors Quality Control program policies, procedures and standards and develops new procedures as appropriate ensuring utilizing best practice standards. Recommends and implements corrective action as required.</p><p>Achieves Quality Assurance objectives by monitoring and assigning day to day activities; identifying and addressing gaps and problems; completing audits; implementing change and providing regular feedback to the CEO regarding system performance and issues.</p><p>Having experience in a licensed cannabis facility in Canada is essential including a current security clearance.</p><p>Industry: Agriculture and Extraction</p><p>Benefits:</p><ul><li>Extended health care</li><li>Dental care</li><li>Life insurance</li></ul><p>Job Types: Full-time, Permanent</p><p>Salary: $80,000.00-$90,000.00 per year</p><p>Benefits:</p><ul><li>Extended health care</li></ul><p>Schedule:</p><ul><li>Monday to Friday</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"name":"Oakum Cannabis Corp"},"location":{"country":"Canada","address":"Kelowna, BC","city":"Kelowna","stateProvince":"BC"},"frontendLink":"/job-posting/oakum-cannabis-corp/quality-assurance-person/0226e678ff14264360a4f01e52fdc117","title":"Quality Assurance Person","category":"Agriculture & Farming","hash":"0226e678ff14264360a4f01e52fdc117","postingUrl":"https://ca.indeed.com/job/quality-assurance-person-e9a87e4fd07c4596"},{"salaries":[{"salaryStart":"$62k","salaryEnd":"$90k","currency":"US","source":"Monster","position":"Quality Assurance Manager","type":"per year","url":"https://www.monster.com/salary/q-quality-assurance-manager-l-modesto-ca"},{"salaryStart":"$69k","salaryEnd":"$100k","currency":"US","source":"Salary.com","position":"Quality Assurance Engineer II","type":"per year","url":"https://www.salary.com/research/salary/benchmark/quality-assurance-engineer-ii-salary/modesto-ca"},{"salaryStart":"$41k","salaryEnd":"$120k","currency":"US","source":"Glassdoor","position":"QA Lead","type":"per year","url":"https://www.glassdoor.com/Salaries/sacramento-qa-lead-salary-SRCH_IL.0,10_IM747_KO11,18.htm"}],"employmentType":"Full-time","function":["Quality Assurance & Regulatory Affairs"],"postedOn":"19 days ago","description":"<div><p><b>The Company</b></p><p>At Canopy Growth, our mission is clear: improve lives, end cannabis prohibition, and strengthen communities. We believe that cannabis can be a force for good. We're building a consumer-centric organization that is focused on sharing the transformational potential of cannabis with the world. We will achieve this through an innovative and disruptive portfolio of cannabis and hemp-derived products.</p><p>With millions of square feet of licensed production capacity and operations spanning four continents, Canopy Growth is the world's leading cannabis and hemp company. We recognize that employees are at the core of our success, and we take pride in a corporate culture that emphasizes inclusiveness, collaboration, and diversity.</p><p>Our employees come from a wide range of backgrounds, each bringing their own unique skills and talents to the table, working together to continue our incredible momentum of growth. If you are interested in building global challenger brands, scaling a business, and working in a values-driven environment, we want to hear from you!</p><p><b>The Opportunity</b></p><p>We are looking for an experienced, highly motivated, self-starter who can take the Laboratory Supervisor position to a new level. If you have sound judgment, great time management skills mixed with the ability to work as part of an ever-growing team we want to hear from you. The lab supervisor ensures the safe, accurate and timely testing of all instrument and production QC samples. The role involves conducting and overseeing the work of lab technician(s).</p><p><b>Responsibilities</b></p><p>• Implement, monitor, and perform calibration of all lab equipment by establishing and ensuring consistent standards of use</p><p>• Facilitate testing of variety of samples with both internal and external labs</p><p>• Review and make decisions based on laboratory results. Present information and findings at departmental meetings as needed</p><p>• Review and develop current and future laboratory operations to improve efficiency and productivity</p><p>• Conduct various testing on ingredients, intermediate &amp; finished products, including chromatographic techniques</p><p>• Support QA and Operations Manager prepare batch production records and lot release reports</p><p>• Work with the QA and Sr. QA Mfg. Manager to review and develop QC operations.</p><p>• Create optimal batches of samples to increase efficiency of instrument run time</p><p>• Data maintenance and thorough logbook and record keeping</p><p>• Generate Certificate of Analysis and Certificate of Conformance for in-process batch releases</p><p>• Input QC and production lab results in LIMS and ERP (SAP) System as required</p><p>• Responsible for maintaining and ordering lab consumables, chemicals and materials</p><p>• Create reports on test results and provide trend analysis on results.</p><p>• Operation of HPLC, GC, GC/MS, pipetting, wet chemistry, and any other required techniques</p><p>• Maintain and calibrate lab equipment on a regular cycle.</p><p>• Ensure test equipment is clean, maintained and in good working order</p><p>• Conduct USP, HPFB and EP microbiological assays for TAMC/TYMC and specific microorganisms.</p><p>• Conduct testing using Karl Fisher titrations or others as required.</p><p>• Communicate equipment and disposables requirements to laboratory supervisor, as required.</p><p>• Analytical laboratory tasks as assigned from time to time.</p><p>• Contribute to method validations.</p><p>• Must be able to work a variable of different shifts</p><p>• Other duties as assigned</p><p><b>Experience</b></p><p>• Bachelors or higher degree in Biology or Chemistry</p><p>• Have a minimum of 2 years' worth of post University hands on experience with Mass Spectrometers</p><p>• Knowledge of routine microbiological methods for the analysis of environmental, agricultural and food samples, including AOAC, FDA, BAM, ISO, PCR or ELISA.</p><p>• Comfortable working in a fast-paced deadline driven environment</p><p>• Detail-oriented and strong time management skills</p><p>• Experience in the preparation of pharmaceuticals, cosmetics and natural health products are an asset.</p><p>• Working knowledge of computer applications including Microsoft Word and Excel</p><p>• Must be meticulous and able to work independently and safely.</p><p>• Knowledge of sample preparation equipment and techniques.</p><p>• Must be comfortable standing for long periods of time.</p><p><b>Other Details</b></p><p>This is a full-time position based out of Modesto, CA.</p><p>We appreciate the interest from all candidates, and promise to review all applications, but we will only be contacting those who best fit the requirements. If you don't hear from us, don't fret; every resume we get is kept in our database for six months for consideration in future searches for talent.</p><p>Canopy Growth welcomes and encourages applications from people with disabilities.</p><p>Accommodations are available upon request for candidates taking part in all aspects of the selection process.</p><p>One last note: the chosen applicant will be required to successfully complete background and reference checks.</p><p>Thank you so much for your interest in Canopy Growth.</p><p>Apply Now</p><p>• Modesto, CA, USA</p></div>","company":{"website":"canopygrowth.com","companyType":"Public/Established","name":"Canopy Growth Corp.","logoUrl":"/logos/canopy-growth-corporation-4824ec81067c68cbe6c52ae1676e4cd3.jpeg"},"location":{"country":"United States","address":"Modesto, CA, USA","city":"Modesto","stateProvince":"CA"},"frontendLink":"/job-posting/canopy-growth-corp/quality-control-lead/77382880afe0ca68948c40fc9c221337","title":"Quality Control Lead","category":"Medical & Healthcare","hash":"77382880afe0ca68948c40fc9c221337","postingUrl":"https://tarta.ai/j/qtdfQnwBPV406l6X3-At-quality-control-lead-in-modesto-california-at-canopy-growth-corp","salary":"$62k - $90k"}]