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Job description
Join Sandoz as a Senior Quality Assurance Specialist and contribute to the company's transformation as a global leader in biopharmaceutical and biosimilar medicines. The role involves monitoring, interpreting, and implementing GMP requirements and pharmaceutical laws, as well as developing and implementing quality management system procedures.
Responsibilities include monitoring GMP requirements, developing quality management system procedures, participating in risk analysis, reviewing change control, and managing quality agreements.
The ideal candidate will have good knowledge of GMP requirements and pharmaceutical laws, be action-oriented and effective in problem-solving, and have a willingness to continuously learn and develop competencies.
Company
Healthcare • Manufacturing
Sandoz is the global leader in generic and biosimilar medicines, delivering high-quality, affordable treatments to over 500 million patients across more than 100 countries. The company focuses on two core businesses—standard and complex generics, and biosimilars—while also offering a range of over-the-counter products. Sandoz differentiates itself by pioneering access to medicines through innovative, sustainable practices and a commitment to tackling global health challenges such as antimicrobial resistance. Its culture of responsibility and community engagement drives continuous improvement and positions Sandoz as a forward-thinking partner in the healthcare industry.
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