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Sandoz Hiring In Specialist in Quality Regulatory Operations

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Your Key Responsibilities:

  • Drafting of Annual Monitoring and Certification report for materials.
  • Drafting and Archival of Quality Assurance Agreement with Suppliers/Service providers.
  • Evaluation and Management of Supplier Change Notifications (SCN).
  • Performing Quality Risk Assessment (QRA) for existing and new Suppliers/Service providers.
  • Management of Supplier/Material qualification and supplier-related documentations.
  • Preparation of regulatory statement for materials and finished products.
  • Management and archival of Quality Questionnaires, QAA, QRA, and Compliance (ASL, Oversight monitoring) for Country Quality.
  • Adherence to the current GxP and compliance requirements of Sandoz.
  • Perform and deliver Quality Operations in support of product quality compliance and regulatory workflows.
  • Support implementing service quality and process improvement projects, CAPA management within GQSI.
  • Regularly communicate with customers and partners to collect feedback on support services and report deliverables.
  • Hold accounts in workflow applications (such as SAP, GxQEM, CONDOR, ESOPs, TrackWise) to ensure appropriate execution of service deliverables.
  • Intensify service-related GxP and non-GxP issues and ensure timely investigation and compliance with local and global operating procedures.

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PharmaBharat Editorial Team

The PharmaBharat Editorial Team, comprised of pharmaceutical industry experts with over 3 years of collective experience in research, regulatory affairs, and market analysis, delivers accurate and timely updates on trends, innovations, and career opportunities. Our content is rigorously vetted by professionals with advanced degrees in pharmacy and biotechnology, ensuring authoritative and trustworthy insights for job seekers in the pharmaceutical sector.