Description
A pharmaceutical company based in the Midlands area is seeking the services of an experienced Validation Engineer to start immediately on an initial 3 month contract.The successful Validation Engineer will be involved in writing validation documents - URS's, IQ, OQ and PQ and must have experience in equipment validation, facilities validation and IT systems.
The key responsibilities for this role include:
- Monitoring ongoing validation exercises and providing regular updates on progress to communicate possible issues that may affect time lines and milestones.
- Ensure that the Validation systems are working in accordance with any changing regulations
- Prepare and review validation protocols and to promptly write reports on completion of execution of the validation/verification duties.
- To review data from validation activities and report them to the Validation Manager.
- Reviewing and approving the relevant documents on validation processes and specifications.
The ideal Validation Engineer will need to have had 2- 3 years experience in general equipment and facilities validation in a Pharmaceutical environment.
To learn more about this excellent opportunity to join a growing pharmaceutical company please send in your current CV to Reshma Patel or alternatively contact myself on