Description
UK based Bio-Pharmaceutical company requires a Validation Lead to join them on an initial 6-month contract.Duties:
- The Successful individual will have supervision of a third party who are providing C&Q services
- The role will include Validation Documentation preparation support
- In addition, the individual will be witnessing Commissioning execution
- They will also be required to ensure documentation is correct
- Experience in leading C&Q activities across mechanical process equipment, facilities and clean & black utilities
- Experience in working with third party suppliers
- Biologics manufacturing experience (Beneficial)