Description
My client a pharmaceutical company based in the South - East area is currently seeking the services of two Validation Specialist, to join on an initial 9 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, 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 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 Specialist will need to have had 2- 3 years experience in general equipment in a Pharmaceutical environment. This role will also require the ideal candidate to have some experience in solid dose and air handling systems within a GMP environment.
To learn more about this excellent opportunity to join a great Pharmaceutical company please send in your current CV or contact directly on