Contract: 09/06/2025 to 31/12/2025
Location: Visp
Language: English or German or both
We are hiring for a Biotechnologist role. This role involves hands-on production of liquid and freeze-dried medicines in a GMP-regulated environment. The person is responsible for operating, setting up, and cleaning equipment, ensuring safe and timely batch production, and following strict quality and documentation standards.
Key responsibilities:
Executing daily manufacturing tasks (compounding, filtration, inspection)
Ensuring compliance with cGMP and batch instructions
Preparing, reviewing, and completing GMP documentation
Supporting investigations, process improvements, and CAPAs
Assisting in training and onboarding new staff
Working closely with teams across production, quality, and technical functions
Must Haves:
2–4 years of experience in GMP/sterile manufacturing
Strong attention to detail and a structured way of working
Fluent in English or German (ideally both)
Team player with good communication skills
Familiar with SOPs, SAP, MES, and GMP documentation
Willingness to work in 2-shift patterns
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