Position:  Project Manager - Quality
Location:  Nanaimo, British Columbia
Job Id:  697
# of Openings:  1

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?
 
PROJECT MANAGER - QUALITY, NANAIMO, BC
 
Reporting to Director, Global Quality, the Global Projects Manager is responsible for overseeing the planning and execution of global quality management systems projects.  Ensure projects are planned and implemented in full compliance with all ACMPR, EU GACP, GMP, GDP, GVP and 21CFR Part 11 requirements as applicable. This role wil also act as the advisor to project teams on the interpretation of quality requirements at different stages of project realization.
 

Role and Responsibilities

  • Drive implementation of IT Quality systems e.g. Trackwise
  • Act as Quality SPoC for new projects
  • Liaise with BizDev for planning and implementation of new contracts/business models
  • Ensure project plans, project scope, resources and roles & responsibilities are defined in accordance with the applicable regulatory requirements.
  • Ensure the needs of the different quality functions at different sites are accounted for during concept development and project execution. 
  • Collaborate with project teams to managing risks and advocates for solutions in compliance with regulatory expectations.
  • Collaborate with business owners to ensure overall performance of the project and project completion documentation is accurate and available
  • Report to senior management on project performance and escalate potential compliance gaps or project delays.
  • Act as a delegate system owner to Global Quality Management System applications and solutions
  • Participate in regulatory inspections and be responsible to present the quality elements of Global Quality Projects

Qualifications 

  • B.Sc./M.Sc. degree in Biological/Life Sciences/Bio engineering (Pharmacology, Molecular Biology, Biology, Chemistry) or extensive experience and related training.
  • 3+ years of project management experience.
  • 5+ years of working experience in a regulated industry.
  • Fluent in English required (oral & written).
  • Good knowledge of cGMP, working knowledge in technical development, production or QA.
  • Excellent organizational and decision-making skills.
  • Proven ability to analyze and evaluate cGMP compliance.
  • Must be a good team player with good communication skills.

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