Quality Manager - Sterile Manufacturing

• 01 septembre 2026
• 100%
• Indefinite duration
• English (Fluent)
• 4001 Basel
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French-speaking Switzerland | GMP | Quality & Compliance ##

Are you looking for more visibility, responsibility, and impact in Quality?

Join a site specialized in sterile pharmaceutical manufacturing where you will work in close collaboration with Production, Quality Assurance, Quality Control, and the Qualified Person, driving GMP compliance and operational quality activities in a highly regulated environment.

Your Responsibilities

• Support batch review and release activities
• Review GMP documentation and manufacturing records
• Manage deviations, CAPA, and change controls
• Provide quality support to production, laboratories, and warehouse operations
• Maintain a strong field presence and drive continuous improvement
• Act as the compliance contact for external customers and partners
• Support customer inspections and audits

Your Profile

• Degree in Pharmacy, Chemistry, Life Sciences, or Engineering
• Experience in regulated GMP pharmaceutical manufacturing
• Good knowledge of sterile / aseptic production
• Experience with deviations, investigations, and change controls
• Operational mindset and willingness to work closely with production
• Fluent French and good English

What is offered

• High-visibility role within a specialized pharmaceutical site
• Broad quality responsibilities with direct impact on operations
• Close collaboration with Production, Quality Assurance, Quality Control, and Release teams
• International environment with short decision-making processes
• Excellent development opportunity towards broader quality and Qualified Person responsibilities