Posted:2 weeks ago|
Platform:
Work from Office
Full Time
1. Planning and preparation of qualification protocols and documents for equipment, instruments, systems, including of utilities, manufacturing process, packing equipment.
2. Review, execution and compilation of qualification protocols and documents for equipment, instruments, systems, including of utilities, manufacturing process, packing equipment.
3. Preparation of yearly and add-on schedule for Periodic Performance Verification-Performance Testing (PPV-PTS).
4. Preparation of yearly and add-on schedule for Periodic Performance Verification-Support Programme Review (PPV-SPR).
5. Follow and ensure compliance of validation SOPs, policy documents and written procedures.
6. Follow and ensure the current Good Manufacturing Practices as per applicable SOPs.
7. Provide training to the personnel involved in qualification and validation activities as & when required.
8. Arrangement, Tracking, Preparation, Review & compliance for the document required for Inspection at site.
9. Co-ordination with CFT for smooth functioning of qualification activity.
10. Any other responsibility that may be assigned by HOD or reporting manager from time to time.
11. Participation in quality improvement projects.
12. Extend need based support to DF Sites, viz. Sun Pharmaceutical Industries Limited (SPIL), India sites and Overseas DF locations.
13. Any other responsibility that may be assigned by HOD or reporting manager from time to time.
Sun Pharma
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