To run the department technically smoothly administratively and according to Good Manufacturing Practice rule and CGMP. To check and control the inprocess through inspection of Quality Assurance. Standard operating procedure compliance for production and warehouse. Vendor, Visit, Audit and Recommendation with Timeline for improvement. Self Inspection & Quality Audit / EHS (Environment Health & Stability) Compliance / Audit. Change control compliance / impact evaluation. Complaint handling. Training of Production, Warehouse, QC Staff & Workers. Periodic product Quality Evaluation. Stability data review. Development of validation protocols, conducting validation exercises and making the process validation compliant. Development of Raw Material, Packing Material, Specifications and specification compliance. Custodian of Production Records. Arching of legal documents, Legal reference sample. Control number allocation & sampling.
Skills Required:
To provide the company with an efficient service with regards to the assurance of the Quality personals and inspection of inprocess under the strictly compliance of GMP rule and standard operating procedure so that the Quality of Product is assured.
Company Information
Company Name:
Opal Laboratories (pvt.) Ltd.
Description:
A local pharmaceutical company having more than 250 employees. Opal Laboratories (Pvt) Ltd, a limited company incorporated under companies Ordinance 1984, having Head office at LC-41 L.I.T.E Landhi Karachi More
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