Vacancy Description
The QC Analyst will be responsible for performing a wide range of testing activities and plays a key part in maintaining cGMP compliance through accurate documentation.
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.
- Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiu...
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