A global Biotech organisation are looking to bring on a Commissioning & Qualification Engineer on an initial 12 month contract basis. This role will be based minimum of 2-3 days on site in Visp.
Key duties & responsibilities:
- Commissioning, Qualification & Validation of equipment, systems & processes
- C&Q Testing
- IQ/OQ/PQ
- Ensuring compliance with GxP, FDA, EMA, ISO standards
- Updating Master C&Q plan
- Identifying risks
- Handover and Release process
Candidate profile:
- 5+ years experience within C&Q/Validation in a Life Science environment
- Used to working with lab instruments
- CSV experience
- Writing CQV documents
- Experience in reviewing IQ/OQ/PQ Protocols
- GMP knowledge
- Knowledge of regulatory requirements
If you'd be interested in discussing further, please send your CV to to set up a call.