**Summary**:- Assurance that the product quality conforms with specifications and that production activity is compliant with Novartis quality policy and GxP requirements.Ensure that relevant documentation is up-to-date and archived correctly.Ensure state of the art GxP know-how and future trends in the field of GxP**About the Role**:**Major accountabilities**:- Ensure that all aspects of the handling, manufacturing and distribution of biopharmaceutical / pharmaceutical products are in compliance with the Novartis Quality Manual, the effective Quality Agreement that they meet relevant GxP regulatory requirements and are conducted according to local SOPs.
- Prepare, review and check the batch documentation for correctness, completeness and safely archive the original documents for the prescribed period and plan, conduct and monitor self-Inspection schemes for all sections.
- Monitor actions and corrections accordingly.
- Conduct GxP monitoring on all sections, conduct QA i...