Job Description
A QA Specialist is required to support a leading pharma company on their manufacturing site, this is an hourly rate 12 month contract with great opportunity for further work.
Main Responsibilities:
1. Reviews routine manufacturing & engineering documentation including batch manufacturing records
2. Support with customer complaint investigations
3. Authoring, reviewing and approving SOPs
4. Identifying & managing deviations & CAPAs
5. Facilitate internal audits & walkthroughs
Qualification & Experience:
6. 3+ years Industry experience across Pharma or Med device
7. Proven knowledge of working within GMP environment
8. Proven experience working in manufacturing environment
9. Must have experience with batch records & tablet manufacturing
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
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