Apply GMP and RCCA expertise to manufacturing investigations at Apotex’s Richmond Hill facility. Produce transparent reports and guide corrective action decisions. The Project Leader ensures investigations are completed efficiently and documented accurately for the Manufacturing and Production departments. You will determine probable root causes, coordinate reviews, and provide support to Operations. Success requires strong written and verbal English, independent prioritization, and regulatory compliance awareness. Key Responsibilities:





Determine probable root causes for completed manufacturing investigations Define corrective and preventative actions for investigation findings Review reports for completeness and accuracy before approval Track progress with Production and Quality Assurance teams Maintain compliance with quality, safety, and ethics requirements Requirements:

Engineering, sciences, or related technical post-secondary degree preferred Manufacturing, engineering, or QA/QC experience preferred Five to seven years in pharmaceutical or manufacturing industry Fluency with project management and RCCA tools Strong written and verbal English command Use root cause analysis, GMP knowledge, and concise reporting to strengthen compliant investigations for Apotex operations.

📌 GMP Root Cause Analysis Leader (Winnipeg)
🏢 Apotex
📍 Winnipeg