Executive - Quality Assurance

13 hours ago

Paonta Sahib, India Sun Pharmaceutical Industries Ltd Full time

Initiation, Review and Approval of SOPs, Specifications, STPs in DCM.
- Initiation, of Specifications, STPs in Laboratory information management system.
- Approval of Artwork and Vendor Proof in Artwork Management System (AMS).
- Review and Approval of All document related to vendor management.
- Initiation & review of Vendor Qualification documents, QM/QI view requests, Code to Code Transfer Requests, Specification Linkage Requests and Shelf-life and retest period extension.
- Preparation of Product Risk Assessment Report.
- Initiation, Review & Approval of Change Management.
- Initiation & QA review of Deviation Management.
- Timely completion of investigations and reports on Market Complaints, change controls, Product Recall, OOS, Deviations and their Compliance.
- Handling of Market complaints and Product Recall.
- Queries response to QP/Customers.
- Compliance to CAPA implementation if any given in the APR against any recommendation.
- Vendor Risk Assessment.
- Preparation of Annual Product Review and timely closure of Annual product review.

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