Description
Equipment Validation Consultant - 12 month contractA large Pharmaceutical company based in Cheshire is seeking an Equipment Validation Specialist, for a 12 month contract to start immediately. You will be involved in writing validation documents - URS's, IQ, OQ and PQ and must have experience in equipment validation.
The Equipment Validation Consultant's key responsibilities will consist of:
- You will be required to monitor ongoing validation exercises and provide regular updates on progress and 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 successful Equipment Validation Consultant will need to have had 2- 3 years experience in general equipment or packaging validation in a Pharmaceutical / Biotech environment. This role will also require excellent communication skills, team working and organisation skills as well as the ability to work independently.
To learn more about this excellent opportunity to join a renowned Pharmaceutical company please send in your current CV to Reshma Patel or call