Biotechnologist

Biotechnologist

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.

Contract: 09/06/2025 to 31/12/2025

Location: Visp

Language: English or German or both

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