Senior Manager, Clinical Product Supply Quality (all genders) (full-time, regular)

📋 Description

• Provide strategic QA oversight for assigned clinical development programs, including quality
• Serve as the senior QA representative on CMC and interdisciplinary product development teams
• Establish and defend risk-based quality positions for complex technical, manufacturing, analytical
• Lead the identification, assessment, and mitigation of quality and supply risks across the product
• Provide QA leadership for internal and external integration activities, including in-licensing
• Lead or oversee quality assessments supporting due diligence activities. Evaluate the

🎯 Requirements

• Bachelor’s degree in life sciences, chemistry, biology, engineering, pharmaceutical sciences, or
• 8+ years industry experience in Quality Assurance, production, testing of active pharmaceutical
• Demonstrated experience in pharmaceutical development, clinical product supply, quality assurance
• Broad understanding of pharmaceutical manufacturing and testing processes, including chemical and
• Experience supporting due diligence, in-licensing, collaborations, mergers and acquisitions
• In-depth knowledge of global GMP requirements and regulatory expectations, including US and EU

🎁 Benefits

• Flexible work models for a healthy work-life balance
• Attractive salary and social benefits
• Comprehensive corporate health management program
• Intensive onboarding with a mentor
• Wide range of career opportunities in an international organization
• Top-tier, attractive development opportunities