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Biotechnology Production Operator

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Onsite

Biotechnology Production Operator

Gi Group

Biotechnology Production Operator

Skills

Compliance

9 days ago

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Important information


Contract type:

Temporary

Location:

3930 Visp, Switzerland

Work mode:

Onsite

Published on:

16 October 2026

What they need


For our renowned industrial partner located in Visp, GI Life Sciences is looking for a Biotechnology Production Operator for a temporary assignment within a demanding and innovative biopharmaceutical environment.

Would you like to be at the heart of pharmaceutical manufacturing processes, in a GMP environment where quality, safety, and performance are key priorities? Then this opportunity is for you!

Temporary position

Start date: 02.11.2026

End date: 30.04.2027

4-shift rotation schedule

Your mission :

As part of the biotechnology production team, you will contribute to the manufacturing of pharmaceutical products while ensuring compliance with cGMP quality requirements and safety procedures.

You will be involved in various stages of the manufacturing process, ensure full traceability of operations, and contribute to the smooth execution of production activities.

Your responsibilities :

  • Perform production operations in compliance with established procedures and cGMP standards.
  • Participate in various activities within biopharmaceutical manufacturing facilities.
  • Identify, analyze, and report deviations or anomalies encountered during production.
  • Execute production steps, perform associated calculations, and complete production documentation.
  • Ensure the accuracy of production records and compliance of manufacturing data.
  • Strictly follow HSE (Health, Safety, and Environment) and quality requirements.
  • Support the onboarding and training of new team members when required.

Your profile :

  • Completed education in Chemistry, Biotechnology, Biopharmaceutical Sciences, or a related scientific field.
  • Initial experience in pharmaceutical, biotechnology, or chemical manufacturing (Operator, Production Technician, Manufacturing Technician, or similar role).
  • Good understanding of GMP/cGMP environments.
  • Strong commitment to quality, safety, and procedural compliance.
  • Professional level of English; German language skills are considered a strong asset.
  • Willingness to work in a 4-shift rotation schedule with flexibility.
  • Team-oriented, detail-oriented, and able to thrive in a dynamic and demanding environment.

If you recognize yourself in this description and would like to join one of Switzerland’s leading biopharmaceutical companies, we look forward to receiving your application.

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