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SalaryA pharmaceutical client is looking for CQV Engineer for an ongoing project, which involves the qualification of process equipment.
This is an initial 6-month minimum contract role with the view to extend.The role has been assessed and is outside IR35.
The role has the following general responsibilities:
- Produce CQV documentation including: CQV Protocols & Summary Reports, SOPs
- Perform field activities including: Attend witness FATs and SATs, execution of CQV protocols
- Walkdown and verification of system drawings (P&IDs, as-builts, etc.)
- Compile data and prepare reports
- Assist in deviation investigations and resolving issues / problems encountered during execution activities
Experience within the Life Sciences sector is a necessity for this position, and it requires someone who has a strong background with equipment / process validation activities.
The interview process is a two-stage one, both conducted via Microsoft Teams, so the client are in a position to move quickly.
If this sounds like the role for you, please apply now!
