Biopharma Manufacturing Operator – GMP Production (Temp)

Job-Room; Schwarzenberg; Vor Ort; CHF 60.000 - 90.000; Teilzeit

Zusammenfassung

Job-Room is seeking a Manufacturing Operator (m/f/d) for a temporary placement in Werthenstein, Switzerland. You will join a GMP-regulated Biopharma production environment, supporting daily manufacturing tasks and ensuring compliance with SOPs and quality standards.

Responsibilities include equipment setup, material handling, sampling, documentation, and collaboration with support groups to maintain smooth production flow. 1 year of pharma/biotech experience and GMP knowledge are required.

Qualifikationen

• 1 year of experience in pharmaceutical or biotech industry or equivalent apprenticeship/education
• Solid understanding of GMP manufacturing processes
• Strong communication in German and English, spoken and written
• Experience in pharmaceutical manufacturing is an advantage
• Reliable, detail-oriented, team-driven work style

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
• Take samples and perform shop floor tasks supporting daily manufacturing operations
• Maintain GMP-compliant status through calibration, maintenance, and checks
• Complete and review batch documentation for proper recording
• Follow area-specific SOPs and work instructions
• Coordinate daily work schedules with support groups
• Handle inventory management, ordering and general shop floor housekeeping

Kenntnisse

German language

English language

GMP manufacturing

Pharma/manufacturing experience

Ausbildung

Pharmaceutical apprenticeship/education

Jobbeschreibung

Job-Room is seeking a Manufacturing Operator (m/f/d) for a temporary placement in Werthenstein, Switzerland. You will join a GMP-regulated Biopharma production environment, supporting daily manufacturing tasks and ensuring compliance with SOPs and quality standards.

Responsibilities include equipment setup, material handling, sampling, documentation, and collaboration with support groups to maintain smooth production flow. 1 year of pharma/biotech experience and GMP knowledge are required.