Mar 26, 2026
Your new company
You will be joining a global biopharmaceutical organisation. Known for its innovation, high‑quality manufacturing, and patient‑focused culture, operating within state‑of‑the‑art GMP facilities supporting sterile manufacturing, biologics production, and advanced therapy programmes.The QC function plays a critical role in ensuring products meet regulatory, safety, and quality standards. You will be part of a collaborative, well‑established team working alongside experienced QC, QA, and manufacturing professionals.
Your new role
As a QC Analyst, you will be responsible for performing routine and non‑routine analytical and/or microbiological testing to support raw materials release, in‑process control, environmental monitoring, utilities testing, and finished product batches.
Conducting analysis using HPLC, GC, UV-Vis, FTIR, and wet chemistry.
Performing bioburden, endotoxin, EM, water testing, and sterility testing in line with GMP.
Completing environmental...
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Unknown Status
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CV-Library
Oxfordshire, UK
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