Description
A pharmaceutical company based in the South - East is seeking an Validation Specialist, to start immediately on an initial 6 month contract.The successful Validation Specialist will be involved in writing validation documents - URS's, IQ, OQ and PQ and must have experience in equipment, process, facilities and utilities validation.
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 Pharmaceutical 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 Quality Assurance Manager.
- Reviewing and approving the relevant documentation on validation processes and general specifications.
The ideal Validation Specialist will need to have had 2- 3 years experience in general validation in a Pharmaceutical environment.
To learn more about this excellent opportunity to join a renowned Pharmaceutical company please send in your current CV to Reshma Patel or alternatively contact myself on