Description
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 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 Engineer will need to have had 4-5 years experience in general equipment and facilities validation in a Medical Device environment. This role will also require the ideal candidate to have an IT systems background with effective communication skills, team working and organisation skills as well as the ability to work independently.
To learn more about this excellent opportunity please contact Sarah Irvine on .