Quality Assurance Specialist

Job description

GMP Quality Operations Specialist (m/f/d) Your Next Step in Pharmaceutical Quality Starts Here – GMP Quality Operations Specialist (m/f/d) Assignment period: 01.11.2026 – 31.10.2028 (temporary) Location: Schachen (LU), Central Switzerland Employment type: Temporary placement through nemensis ag About our client Our client is an internationally active pharmaceutical company in Central Switzerland, operating in a highly regulated GMP environment and known for its strong quality culture and global manufacturing excellence – a great place to grow as a GMP Quality Operations Specialist (m/f/d). Your tasks As GMP Quality Operations Specialist (m/f/d), you play a key role within the Quality Operations team: Support compliance-based quality programs and cross-functional initiatives Contribute to release/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 Your 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 at least 3 days/week (hybrid) What you can expect from nemensis Nemensis AG is your specialized personnel service provider in Life Sciences, based in Basel Comprehensive guidance throughout your application process by our consultants Access to a broad client network and exciting roles across Northwestern Switzerland Fast, straightforward entry thanks to individual coaching At nemensis ag, we've connected thousands of candidates with their dream job. What can we do for your career today? Get in touch about this GMP Quality Operations Specialist (m/f/d) role in Schachen (LU)!