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You will be updated with latest job alerts via emailResponsibilities:
Issuance of Sops formats Logbooks Specifications and other documents.
Handling PQS including Change control management Quality risk management Deviation investigations Incidents Market complaints CAPA and also maintain track of CAPA trend analysis of deviations Market complaints/OOS/OOT etc.
Issuance and retrieval of BMR and BPR in absence of a concerned person.
To maintain training documents.
Preparation review and retrieval of Sops.
Updation of induction training record certified training record on job training and training need identification record.
Stability studies management including samples charging in chambers samples withdrawn for analysis as per Schedule Schedule preparation of new products and collection and review of stability data per maintain protocols maintain cleaning record of stability chambers and stability reports retrieval per station.
To maintain control of the sample room.
Daily monitoring of temperature and humidity of the control sample room.
To maintain the destruction record of control samples and also ensure the destruction of samples as per schedule.
Retrieval of specifications and Standard test procedures.
Updation of Equipment lists Self inspection planners technical staff and Internal trainer list.
To maintain JDs/ Signature log/ Organograms/ Layouts/ QTA/ Contracts etc.
Handling of RA related queries.
and Maintain Compliance Reports /internal selfinspection as per schedule under supervision of ManagerQA.
Approval of shade cards in absence of a concerned person.
The executive will look after the above mentioned responsibility in absence of Officer QA.
Any other job as and when assigned by ManagerQA
24 Years (Up to 3 LPA)
56 Years (Up to 4.2 LPA)
Required Experience:
Senior IC
Full-Time