Work Location - Baddi, Baroda & Navsari
Ensure GMP/GLP compliance at Contract Manufacturing sites and third party sites and provide registration documents and required support for registration from site.
- Ensure availability of current valid master documents like raw material /packing material /finished product specifications batch manufacturing record /batch packing record at site and retrieval of obsolete documents.
- To check and find non compliances at Contract Manufacturing /Third Party location and ensure corrective and preventive action.
- To execute, ensure and monitor process validation / Technology Transfer activities, Unit Operation, QMS Compliance at site and arrange for the reports.
- Preparation and submission of annual product review report for Contract Manufacturing products manufactured at site.
- Visit at Third party manufacturing sites for product data review and COA.
- Co-ordinate with PPIC, Nasik QA office and PDC for routine activities and queries.
- Verification of RM/PM testing as per GPL specification & Sampling Plan at Contract Manufacturing /Third Party Site and approval of site master documents, Training to be given for shop floor persons related to change implementation in BMR, BPR to execute the quality product & GMP process at LL/ TP site
