Drive quality management for Roche as a Technical Manager focused on APQR processes. You'll conduct in-depth product reviews, ensuring compliance and quality across the board.

This 12-month contract role at Roche requires a B.A. or B.S. in Life Science and 3-5 years of experience in cGMP pharmaceutical or biopharmaceutical settings. You'll lead cross-functional teams to address complex quality issues while developing and maintaining Global APQR systems. Your role is central to optimizing data through visualizations and analytics, directly impacting the quality of Roche's commercial products.

Key Responsibilities:
• Conduct annual APQR reviews for Roche products
• Compile detailed APQR reportsusing data from various sites




• Identify and resolve product quality issues collaboratively
• Support administrative activities of Global APQR projects
• Ensure compliance with cross-functional deliverables

Requirements:
• B.A., B.S. or higher degree in Life Science
• 3-5 years in cGMP/pharmaceutical industry
• Expertise in drug manufacturing and control systems
• Experience with analytics and compliance reporting
• Ability to lead without formal authority

Become a vital part of Roche, shaping future healthcare solutions with your technical expertise and leadership.
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📌 Technical Manager APQR at Roche (Ontario)
🏢 F. Hoffmann-La Roche
📍 Ontario