Posted:3 weeks ago|
Platform:
Work from Office
Full Time
Preparation of Site Master File, Validation Master Plan and execution as per Plan, Preparation of Quality Manual & approved by QA Head, to prepare the standard operating procedures for conformance with good manufacturing practices & good laboratory practices. To take active part in conduction of an internal audit to ensure compliance to good manufacturing practices & other regulatory requirement, to review the market complaints.To review the product recall, To participate in validation of processing equipment, cleaning equipment, process & cleaning procedures are done on timely basis, to carry out the documentation in compliance with good manufacturing practices, provide the required documents to regulatory department.
Icpa Health Products
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