Product Quality Lead– Pharma, GMP, Lifecycle Management

6-Month Temporary Contract | Basel

Our client is a leading biopharmaceutical company dedicated to providing innovative treatments for rare diseases. To strengthen their Global Quality team, they are seeking an experienced Product Quality Lead (m/f/d) for a 6-month contract. This role will be split between leading a quality improvement project and managing product quality oversight for commercialized pharmaceuticals.

Your Role & Responsibilities

Quality Improvement Project (50%)

• Lead a cross-functional quality improvement initiative focused on streamlining change control handling in regulatory dossiers and release processes.
• Ensure compliance with GMP regulations and pharmaceutical quality standards.
• Provide project management support, including planning, scheduling, and coordination of activities.
• Collaborate with stakeholders to drive process efficiency and ensure successful implementation.

Product Quality Lead Responsibilities (50%)

• Act as key Quality Assurance contact for 1-3 medicinal products, ensuring compliance throughout their lifecycle.
• Provide assessment, guidance, and regulatory oversight on all product quality aspects.
• Support cross-functional teams involved in product lifecycle management.
• Ensure audit and inspection readiness in collaboration with internal teams.

Your Profile

• Educational Background: University degree (minimum 4 years) in Pharmacology, Biochemistry, Chemistry, Chemical Engineering, or equivalent.
• Industry Expertise: At least 5 years of Quality Assurance experience in commercial pharmaceuticals under GMP.
• Regulatory & Compliance Knowledge: Strong understanding of EU/FDA GMP requirements, regulatory dossiers, and release processes.
• Project Management: Proven track record in pharmaceutical project management, ideally with complex supply chains & CMO/CLO management.
• Communication & Leadership: Excellent stakeholder management skills, with the ability to work collaboratively in a global team environment.
• Language Skills: Fluent in English (spoken & written).

What’s in for You?
✅ 6-month interim contract in a global biopharmaceutical company.
✅ Exciting opportunity to lead a high-impact quality improvement project.
✅ Work in Basel, Switzerland, with a flexible hybrid model (minimum one day on-site required).
Are you ready to take on this high-impact Quality Assurance role? Join a leading pharmaceutical company and drive excellence in GMP compliance.