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Our client, a leading pharmaceutical manufacturing company based in Dublin are hiring a QA Manager on a 12 month contract.
Check out the role overview below If you are confident you have got the right skills and experience, apply today.
The QA Manager will join a team providing end-to-end oversight across a complex and global supply footprint. The role ensures the delivery of safe, high-quality products to patients by maintaining compliance across all stages—from early-phase clinical trials to commercial manufacturing and distribution. The position focuses on overseeing quality for external manufacturing of Drug Substance (DS), Drug Product (DP), and Finished Dosage Form (FDP) for both small and large molecules.
Key Responsibilities- Maintain global GMP/GDP licenses and ensure compliance for external suppliers.
- Manage and update Quality Agreements with outsourced partners.
- Approve deviations, change controls, and QMS documents with proper follow-up.
- Coordinate mock recalls and implement corrective actions for deficiencies.
- Support operational excellence programs and continuous improvement initiatives.
- 4+ years of quality and manufacturing experience in biotech or pharmaceutical industry
- Bachelor’s Degree in a Science Field
- Knowledge of cGMP and manufacturing/testing processes (API, DS, DP, Packaging, Device). xcfaprz
- Ability to manage multiple projects, deliver on time, and operate in team/matrix environments.
- Familiarity with project management tools and willingness to travel ~10%.
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Sprachkenntnisse
- English
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