The QC Analyst will be responsible for performing a wide range of testing activities and role plays a key part in maintaining cGMP compliance through accurate documentation,
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This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. Normal working hours apply; however, candidates must be flexible to work 12-hour shifts when required based on business needs.
What you’ll get
An agile career and dynamic working culture in a global life sciences leader.
An inclusive and ethical workplace that values diversity and integrity.
Competitive compensation programs that recognize high performance.
Professional growth opportunities through cross-functional projects and global exposure...