QA Manager Pharma / Batch Release, GMP & Validation

About the job

Responsibility - Overview - Learnings

Your next step in quality assurance – with more responsibility, but without corporate overload.

You already have experience in pharmaceutical quality assurance and want to take the next step? Take on more responsibility, be closer to decisions, and contribute your know-how in a dynamic environment?

Then this could be exactly your move.

Your tasks

• Responsibility for batch record review and approvals
• Collaboration and further development of QA processes in the GMP environment
• Support and execution of deviations, CAPAs and change controls
• Participation in validation activities and risk analyses
• Cooperation with production, QC and other interfaces
• Support during audits and inspections

Your profile

• Initial to several years of experience in QA within the pharma/biotech industry
• Good knowledge of GMP guidelines
• Experience with batch review, documentation or validation is an advantage
• Structured, solution-oriented working style
• Fluent in German and English in everyday work

Important: You don’t have to be an "old hand" – we are deliberately looking for candidates with development potential.

What to expect

• Exciting mix of operational QA and project work
• Opportunity to develop towards Senior QA or specialist (e.g. validation, compliance)
• Short decision-making paths and visible impact
• Stable employer with a clear future perspective
• Attractive overall package

Why this role?
Many QA roles are either too operational or already strongly strategic.
Here you get exactly the right mix to develop professionally and career-wise without committing too early.