Biopharma GMP Manufacturing Operator

nemensis ag Schweiz; Werthenstein; Vor Ort; CHF 60.000 - 80.000; Vollzeit

Benefits dieser Stelle

Consultant support

Client network NW Switzerland

Career coaching

Zusammenfassung

Nemensis AG Schweiz is seeking a Manufacturing Operator (m/f/d) for a temporary placement to support the Drug Substance Bioprocess team in a GMP environment. You will set up and operate manufacturing equipment, manage materials, and ensure documentation and compliance on the shop floor.

The role requires at least 1 year in pharma/biotech, strong GMP knowledge, and fluency in German and English. Join a team focused on quality and patient outcomes in Northwestern Switzerland.

Qualifikationen

• At least 1 year of experience in the pharmaceutical or biotech industry, or an equivalent apprenticeship/education.
• Solid understanding of GMP manufacturing processes.
• Strong communication skills in German and English, spoken and written.
• Reliable, detail-oriented, and team-driven approach.

Aufgaben

• Set up, prepare, and operate manufacturing equipment as part of a cross-functional production team.
• Prepare components and manage materials to keep production running smoothly.
• Take samples and perform shop floor tasks that support daily manufacturing operations.
• Keep equipment in GMP-compliant status through routine monitoring, calibration, and maintenance.
• Complete and review batch documentation to ensure production activities are properly recorded.
• Familiarize yourself with and follow area-specific SOPs.
• Support the coordination of daily work schedules with relevant support groups.
• Handle inventory management, ordering, and general housekeeping on the shop floor.

Kenntnisse

GMP manufacturing processes

German speaking

English speaking

Attention to detail

Team collaboration

Ausbildung

Pharmaceutical apprenticeship or related education

Jobbeschreibung

Nemensis AG Schweiz is seeking a Manufacturing Operator (m/f/d) for a temporary placement to support the Drug Substance Bioprocess team in a GMP environment. You will set up and operate manufacturing equipment, manage materials, and ensure documentation and compliance on the shop floor.

The role requires at least 1 year in pharma/biotech, strong GMP knowledge, and fluency in German and English. Join a team focused on quality and patient outcomes in Northwestern Switzerland.