GMP Quality Operations Specialist (m/f/d)

nemensis AG; Schachen; Hybrid; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

nemensis ag is seeking a GMP Quality Operations Specialist (m/f/d) to join the Quality Operations team. You will support compliance-based quality programs and cross-functional initiatives in a highly regulated GMP environment.

Responsibilities include contributing to release/rejection decisions for GMP materials, reviewing documentation and quality records, and maintaining quality systems. The role requires a university degree and fluent German (C1), with a hybrid on-site work arrangement (at

Qualifikationen

• Fluent German (C1) mandatory.
• University degree (Bachelor's or higher) preferred.
• On-site at least 3 days/week (hybrid).

Aufgaben

• 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.

Kenntnisse

German (C1)

Ausbildung

Bachelor's degree or higher

Jobbeschreibung

GMP Quality Operations Specialist (m/f/d)

Your Next Step in Pharmaceutical Quality Starts Here – GMP Quality Operations Specialist (m/f/d)

• 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).

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
• Reliable, structured and detail-oriented way of working
• On site at least 3 days/week (hybrid)