1. To Co-ordinate with all Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D, QC, AR&D for closure of QMS like CAPAs, Investigations”, Deviations in set time as per SOP.
2. Preparation of “Risk Assessment” and Impact Assessment report as per requirement.
3. To Co-ordinate with all Production Blocks, Maintenance, Process Engineering, QA, CQA, PR&D, QC, AR&D for initiation of QMS like CAPAs, Deviations as per requirement.
4. Follow the cGMP compliance by following the SOPs and approved procedures.
5. Responsible for any activities assigned by Manager.
