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.

• 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...