Description
Validation Specialist - 6 month contract - South- EastA pharmaceutical company based in the South - East area is seeking an Equipment 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 validation, particularly solid dose.
The key responsibilities for this role include:
- Monitoring ongoing validation exercises and providing regular updates on progress to communicate possible issues that may affect timelines 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 Specialist will need to have had 2- 3 years experience in general equipment and facilities validation in a Pharmaceutical environment. This role will also require the ideal candidate to have some experience in solid dose within a GMP environment.
To learn more about this excellent opportunity to join a renowned Pharmaceutical company please send in your current CV to Reshma Patel or contact myself on