
Project Engineer CAPEX - Biopharmacutical Manufactering - VISP
Switzerland
Apply by 18 Jun 2026
Competitive
Job Ref.: BH-57395
Job Description
Project Details:
- Focus: Leading technical modifications, managing change controls, and driving the CQV (IQ/OQ/PQ) phase for a commercial production line upgrade.
- Duration: 7-month initial contract (ASAP through Dec 2026).
- Location: 100% On-site in Visp.
- 5 years of experience in biopharmaceutical manufacturing, focusing on technical project management or operational excellence.
- Proven experience working on GMP-compliant projects, including change management and qualification activities.
- Hands-on experience in commissioning, qualification, and validation (CQV) of equipment and processes in a GMP environment.
- Strong knowledge of GMP regulations and biopharmaceutical manufacturing processes.
German lanuage is highly beneficial
We believe in equal opportunity for all and actively encourage applications from diverse backgrounds, experiences, and perspectives.
Source Group International Ltd is acting as an Employment Business in relation to this vacancy