
Job description
Manages Quality aspects and projects within area of responsibility, ensuring overall GxP conformity and Compliance with the Sandoz Quality Management Systems.
Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance, Review and approval of production, QC, and AS and T records, MBR review, Executes batch release in compliance with registration, Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt, Distribution of marketing samples (where applicable).
QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &., Collaborating across boundaries, cleanliness zones, Continuous Learning, Dealing With Ambiguity, Gmp Procedures, QA (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence.
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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