Lead Quality Control programs in the pharmaceutical industry as an Associate Director. Focus on drug development compliance and management of stability studies, ensuring adherence to ICH and cGMP standards.

In this role, you will manage key Quality Control processes, guide teams through analytical evaluations, and support the stability study framework. Experience with master specifications and OOS/OOT investigations is crucial. Collaboration with cross-functional teams enhances regulatory compliance and product release efficacy.

Key Responsibilities:
• Direct Quality Control activities in drug programs
• Manage stability studies and quality checks for product release
• Lead investigations for any quality deviations
• Compile detailed reports with analytical results
• Supervise team efficiency and performance reviews

Requirements:
• Undergraduate degree in life sciences
• 8+ years of experience in quality management
• Expertise in quality testing and stability management
• Proven leadership capabilities in teams
• Travel required up to 20%

Utilize your pharmaceutical experience and leadership skills to elevate quality assurance standards.
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📌 Associate Director, Quality Control Programs (British Columbia)
🏢 Jobtailor
📍 British Columbia