Technical QA Manager Annex 1 Project | Technischer QA Manager Annex 1 Projekt
ELAN Personal AG
Job Summary
This is a critical contract opportunity for an experienced Technical QA Manager to join the IMP Quality - Qualification/Validation Team at a leading pharmaceutical company in Basel. Focusing specifically on the Annex 1 Project concerning sterile filling operations, you will ensure the GMP compliance of existing and new equipment and systems. Key responsibilities include providing QA oversight for qualification and validation activities related to GMP-relevant systems, including CSV systems, and supporting the implementation of data integrity requirements. You will be responsible for reviewing and approving crucial GMP documentation such as qualification plans, reports, change/deviation management, CAPAs, and SOPs. This role demands collaboration with diverse stakeholders, representing the area during health authority inspections and internal audits, and requires proven success in navigating regulatory scrutiny. Fluency in both German and English is a mandatory prerequisite for success in this highly regulated environment.
Required Skills
Education
Academic degree in Engineering, Chemistry, Life Science, Pharmacy, or equivalent
Experience
- Minimum 5 years of experience in the pharmaceutical industry
- Minimum 2 years of experience in Quality Assurance
- Experience in equipment qualification and validation in the manufacturing of sterile medicinal products
- Proven success in handling inspections by health authorities and internal GMP audits
Languages
Additional
- Contract duration: January 2026 - July 2026. Must be a strong team player with excellent communication and influencing skills.
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