Validation Consultant - Midlands

19 Mar 2013
16 Apr 2013
Hemish Ilangaratne
Full Time

My client, a growing pharmaceutical organisation based in the Midlands is seeking a Validation consultant for a period of 12 months.

Working within the Quality department, the role will require someone with extensive Equipment and Process Validation experience with a strong GMP background, particularly within solid dose manufacturing. A candidate with CSV experience would be particularly beneficial. Additionally, someone with experience of using Enterprise Resource Planning and writing test scripts would be useful.


- 8-10 years validation experience within the pharmaceutical industry

- Strong GMP/Solid dose manufacturing background

- Detailed IQ,OQ,PQ knowledge and understanding

- Project management experience

- CSV/Electronic Resource Planning experience (beneficial but not essential)

Interviews will commence on the week commencing the 8th April, with a view to start as soon as possible thereafter.

If you are interested in this opportunity, please contact Hemish Ilangaratne on 020 7758 7322 with an updated CV. Please also forward this on to anyone who may be interested - we offer £200 of vouchers for any successful referrals.

Best regards

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