Clinical QA Specialist (Pharmaceuticals)

Hampshire  ‐ Onsite
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Keywords

Description

Available immediately.  Great opportunity to provide QA support for the manufacture, packaging, labelling and control of clinical trials materials manufactured by subcontractors to ensure compliance with GMP requirements. In addition you will be providing QA support to contract laboratories and to perform GMP release of IMP, ensuring compliant release to global markets.

To be successful you will have a university degree in Chemistry, Biology or other relevant science and/or on the job experience.  You are unlikely to have less than 8 years' experience in a Pharmaceutical QA environment.  You must also have clinical, manufacturing, packaging and/or labelling experience in particular the manufacturing of solid dose pharmaceutical products.  GMP understanding within a global environment is also key.

Travel will be necessary for audits and other quality related visits.  Some overseas travel may be required.  Please contact us to hear more about this great opportunity.
Start date
NOW
Duration
3 Months +++
(extension possible)
From
Taylor Mclaren
Published at
12.10.2012
Project ID:
433320
Contract type
Freelance
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