Your Next Step in Pharmaceutical Quality Starts Here
Join an internationally active pharmaceutical company in Central Switzerland, operating in a highly regulated GMP environment. Known for its strong quality culture and global manufacturing excellence, this organization offers a significant opportunity to grow within a dedicated Quality Operations team.
Key Responsibilities
- Support compliance-based quality programs and cross-functional initiatives
- Contribute to release and rejection decisions for GMP-relevant materials, including critical issue support
- Review documentation, systems, and GMP-relevant records
- Help maintain and improve quality systems, directives, and site procedures
- Ensure work meets the highest standards of integrity, quality, and GMP compliance
Required Profile
- Previous experience in a similar quality role within a regulated environment is an advantage
- University degree (Bachelor's or higher) preferred
- Fluent German (C1) mandatory
- Business-proficient English expected
- Reliable, structured, and detail-oriented way of working
- On-site presence at least 3 days per week (hybrid model)
What You Can Expect
Work with a specialized personnel service provider in Life Sciences based in Basel. Benefits include comprehensive guidance throughout the process by consultants, access to a broad client network and exciting roles across Northwestern Switzerland, and fast, straightforward entry thanks to individual coaching.