Posted:1 day ago|
Platform:
Work from Office
Full Time
Work Location - Baddi, Baroda & Navsari
Ensure GMP/GLP compliance at Contract Manufacturing sitesand third party sites and provide registration documents and required support for registration from site.
Ensure availability of current valid masterdocuments like raw material /packing material /finished product specificationsbatch manufacturing record /batch packing record at site and retrieval ofobsolete documents.
To check and find non compliances at Contract Manufacturing /Third Party location and ensure corrective and preventive action.
To execute, ensure and monitor processvalidation / Technology Transfer activities, Unit Operation, QMS Compliance atsite and arrange for the reports.
Preparation and submission of annual productreview report for Contract Manufacturing products manufactured at site.
Visit at Third party manufacturing sites forproduct data review and COA.
Co-ordinate with PPIC, Nasik QA office and PDCfor routine activities and queries.
Verification of RM/PM testing as per GPLspecification & Sampling Plan at Contract Manufacturing /Third Party Site and approval of site masterdocuments, Training to be given for shop floor persons related to changeimplementation in BMR, BPR to execute the quality product & GMP process atLL/ TP site
Glenmark Pharmaceuticals
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