Key Responsibilities Include:
- Manage GMP batch release of commercial products in Canada
- Oversee Quality System documentation (SOPs, Quality Agreements, Site Master Files)
- Support internal and external audits, Health Canada inspections, and license renewals
- Collaborate with global and local cross-functional teams (Regulatory, QA, Supply Chain)
- Drive inspection readiness, CAPA management, and quality performance tracking
- Handle product recalls, customer complaints, and continuous training programs
Required Background:
- 7–8+ years in QA roles within the pharma or biotech industry
- Experience with GMP/GDP; familiarity with GVP, GCP, or GLP preferred
- Strong leadership, compliance, and cross-functional collaboration skills
- Bachelor’s in a life science or related field
Job Type: Fixed term contract
Contract length: 24 months
Pay: $50.43-$65.00 per hour
Experience:
- GMP/GDP: 5 years (required)
- Quality Systems Oversight: 4 years (required)
- , Inspection Readiness: 3 years (required)
- Canadian Product Distribution: 3 years (required)
Work Location: In person
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