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Job Description & How to Apply Below
Talentmark are recruiting for an QA Administrator, to join a pharmaceutical company, based in Birmingham, on a permanent basis.
The salary is around 27,000- 29,000 per annum.
The Company:
Our client are a Pharma manufacturing company who produce, import, and distribute bespoke medicines (Specials), and CBPMs (Cannabis-Based Products for Medicinal Use).
Your main duties will be:
- Manage the lifecycle of all controlled documents within the paper-based QMS (SOPs, forms, master documents, batch records, policies and specifications).
- Provide administrative support for deviations, NCs, CAPAs, change controls, complaints and incident reports.
- Ensure document activities comply with EU GMP (as applicable to Specials), MHRA expectations, and internal quality procedures.
- Work closely with Production, QC and QA teams to ensure correct and timely use of controlled documents.
- Design and execute method validation/verification, method transfers and robustness studies as required.
Your Background (Essential):
- Degree in scientific, pharmaceutical or quality-related discipline.
- Previous administration experience in an office or documentation-focused role.
- Strong command in Microsoft Excel.
Your Background (Desireable):
- Familiarity with core GMP documentation.
- Experience in a GMP, pharmaceutical, specials or other regulated environment.
- Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence.
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