Commissioning & Qualification Engineer

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.