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This job expired on 22/07/2026. It no longer accepts applications.

Production Operator

CK QLS · Lucerne

Junior 🇬🇧 English
GMP manufacturing batch documentation

Job description

About the role

We are seeking a Production Operator to join a global biopharmaceutical company in Lucerne for a 12‑month assignment, with the possibility of extension. The role is part of the Biologics Manufacturing Science and Operations department, focusing on drug substance bioprocesses.

Key responsibilities

  • Support cross‑functional teams in equipment operation during manufacturing, including component preparation, equipment setup, sampling, and material management.
  • Maintain GMP status of equipment through routine monitoring, calibration, maintenance, and certification.
  • Review and complete batch documentation to support production activities.
  • Familiarise with and follow area Standard Operating Procedures (SOPs).
  • Coordinate daily work schedules and organise collaboration with support groups.
  • Manage inventory and order supplies as needed.

Required profile

  • At least 1 year of experience in the pharmaceutical or biotech industry, or equivalent apprenticeship/education.
  • Familiarity with GMP manufacturing processes.
  • Good verbal and written communication skills in German and English.
  • Additional 2‑3 years of pharmaceutical manufacturing experience is advantageous.

Required skills

  • GMP manufacturing knowledge.
  • Equipment calibration and maintenance.
  • Batch documentation handling.

Questions fréquentes

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Published 4 months ago

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CK QLS

Lucerne