Posted:2 months ago| Platform:
Work from Office
Full Time
1. Handling of quality management system (Change Control system, Deviation, Incident & other related documents). 2. To follow and implement good documentation practices. 3. To prepare the Validation Master Plan, Site Master File and other documents related to QAD. 4. To prepare and review validation protocols, execution of the activity and reports summarization. 5. Preparation & implementation of SOPs related to the QAD. 6. To investigate market complaints and to maintain market complaints investigation records. 7. To issue, control, review and retrieval of Formats, Log books, Batch records & Protocols etc. 8. To verify dispensing of materials and In-process quality control, online entries in BMR & BPR of product at manufacturing site. 9. To give line clearance before starting of the activity related to batch. 10. To ensure the handling of non-conformity as per defined procedure. 11. To plan the internal audits and self-inspections of the manufacturing facility to ensure that the facility meets the required quality standards as per the procedure. 12. To prepare and review qualification / re-qualification protocols and reports. 13. To review the artworks and shade cards. 14. To execute documentation as per procedure for approval of new manufacturer / supplier / vendor meant for raw material, primary packing material or secondary packing material. 15. To obey any task assigned by reporting manager.
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