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Specialist Quality Control
Posted 1 month ago
Job summary
Support stability programs and perform quality control testing of pharmaceutical products under GMP conditions, involving analytical activities such as HPLC, GC, dissolution, and wet chemistry, with responsibilities including data review, reporting, and compliance with GMP and SOP standards.
Responsibilities
The specialist will perform analytical activities for the stability program of drug products under GMP conditions. Responsibilities include writing stability summaries, protocols, and reports, as well as managing laboratory supplies and data checking.
Qualifications
Candidates must hold a relevant qualification such as an HNC, HND, or Science Degree and possess demonstrated technical competence in analytical techniques like HPLC and GC. Experience within a pharmaceutical or biotechnology industry and a strong understanding of GMP/GLP environments are highly desired.
Benefits
- Private Medical Insurance
- Health Cash Plan
- Contributory pension scheme
- Life Insurance
Company
NextPharma
- Location
- East Calder, Scotland, United Kingdom
- Website
- nextpharma.com
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