Direct pharmaceutical Quality Control initiatives, managing compliance with ICH and cGMP requirements. This associate director role focuses on overseeing stability programs and analytical result management.

You will lead critical Quality Control functions, managing stability studies while fostering effective cross-team collaboration. A robust understanding of compliance frameworks and quality testing is essential for this role. This position involves significant mentorship and leadership responsibilities, ensuring team performance and adherence to industry regulations.

Key Responsibilities:
• Manage Quality Control operations for drugs
• Lead stability activities and analytical assessments
• Organize OOS and OOT investigations




• Facilitate audits with external laboratories
• Ensure compliance for regulatory submissions and workflows

Requirements:
• 8+ years’ management experience in pharmaceuticals
• Knowledge of stability program management
• Expertise in quality control processes
• Strong leadership and mentoring skills
• Willingness to travel up to 20%

Assert your expertise in Quality Control and leadership to ensure the highest standards of pharmaceutical product integrity.
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📌 Pharmaceutical Quality Control Director (British Columbia)
🏢 Jobtailor
📍 British Columbia