Position:  Quality Compliance Associate
Location:  Toronto, Ontario
Job Id:  1168
# of Openings:  1

Quality Compliance Associate - Toronto, Ontario
Tilray is a federally licensed producer of medical cannabis. We are committed to setting the gold standard of care and excellence in our industry. We believe that commitment starts with a great work environment and benefits for our associates.
Looking to develop your career at the forefront of a rapidly expanding industry?
Ready to apply your talents to make a positive difference in the lives of patients across the country?
Reporting to the Global Third-Party Manager, Quality Compliance Associate performs supplier management quality and compliance activities of licensed producers of Cannabis, suppliers of API, excipients, packaging components, and firms providing GMP services such as laboratories and others as required, to ensure products and services meet quality and compliance standards. Prepares Quality Agreement templates, paper-based audit reviews, and communicates findings to external and internal stakeholder. Able to work independently or as part of a team.
Roles and responsibilities
  • Conducts quality assessment of supplier qualification files
  • Provide GMP/ GPP expertise and experience to Tilray Inc. on the status of compliance of the supplier files
  • Maintain supplier matrix, performs paper-based audits, communicate with the auditee and request additional documents, as required
  • Independently perform evaluations of quality systems and practices in compliance with (GMP, ICH, CFR, IPEC, GACP, etc.), coordinates resolutions, and provides guidance on quality/compliance risk levels
  • Prepares vendor assessment reports and communicates findings to external and internal stakeholders
  • Updates the Global Supplier Managements tools e.g. Approved Vendor List and Audit databases
  • Participates in the development of QA programs, auditing tools (checklists, questionnaires, policies, SOPs and controls
  • 3+ years of relevant experience in the pharmaceutical industry and a BSc degree
  • Minimum 2 years QA experience in the pharmaceutical or cannabis industry
  • Prior knowledge of the requirements of ICH Q10 (plus ICH Q8 and ICH Q9)
  • Prior knowledge of Change Management principles and supplier quality monitoring
  • Knowledge and experience working within a pharmaceutical manufacturing, packaging, and/or warehousing GMP Quality Management System
  • Knowledge of the EU-GACP and Canadian Cannabis Regulations, Cannabis Act, Food and Drugs Act and Regulations, Controlled Drugs and Substances Act and Regulations
  • Excellent communication skills - written and verbal
  • Fluent in English, additional language is a plus
  • Travel approximately 20%

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