Drive Quality Control initiatives at the associate director level, focusing on compliance with ICH and cGMP standards in the pharmaceutical sector. Lead stability programs and oversee analytical evaluations to ensure product integrity.

This role requires expertise in managing Quality Control processes, as well as strong leadership over cross-functional teams and external relationships. Candidates should possess a rich background in pharmaceutical quality assurance, specifically with small molecules or biologics, and experience in stability studies. Your contributions will significantly impact product development and compliance practices.

Key Responsibilities:
• Oversee Quality Control activities for drug substance and products
• Manage master specifications and stability program compliance




• Lead investigations for OOS and OOT events
• Facilitate audits and interactions with external testing labs
• Ensure regulatory compliance across multiple submissions

Requirements:
• 8+ years in pharmaceutical management
• Robust background in quality control testing
• Experience with stability programs per ICH
• Excellent communication skills, both oral and written
• Ability to travel domestically and internationally up to 20%

Contribute your extensive knowledge in quality control and compliance to ensure successful drug product launches.
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📌 Quality Control Lead in Pharmaceuticals (British Columbia)
🏢 Jobtailor
📍 British Columbia