Validation Consultant - 9 Month Contract

England  ‐ Onsite
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Keywords

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
Start date
12/2014
Duration
9 Months
From
Real Staffing
Published at
12.12.2014
Project ID:
822181
Contract type
Freelance
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