MANAGER

0- 15 years in Pharmaceutical industry B. Pharm/ M. Pharm/ M. Sc (Organic/ Analytical Chemistry)

Best in Industry Job Responsibilities Preferably working with Parenteral / Solid dosage manufacturing plant, responsible for conducting audits in plant, to implement cGMP system, to train QA personnels, monitoring of QA functions, to ensure that pharmaceutical products manufactured by the company meets the quality standards, Responsible for preparation, approval and compliances of following documents and records

1) Standard Operating Procedures. 2) Protocols (Process Validation, Equipment Validation and stability). 3) Annual Product Review. 4) Vendor Approval (RM and PM) Forward your Resume to

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