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The Director of Sai Pharmaceutical Consultants, Mrs. Vijaya Shinde entered the Pharma industry through US Vitamins India Ltd. After U S Vitamins Ltd., and a 20 years successful career with Johnson & Johnson Ltd. as a Senior QA Manager she supported Dishman pharmaceuticals, Ahmedabad as Vice President, QA, QC, ADL, RA.

Dishman Pharmaceuticals is a 100% Export Oriented Unit engaged in Manufacturing of Phase Transfer catalysts, Specialty Chemicals & Bulk drugs. The Quality systems here were established under her Leadership and guidance.

She has worked as CORE TEAM member & as Auditee for USFDA, EDQM & WHO GMP audits .

She was successful in all Regulatory & Customer Audits from Top Multinational companies which include Merck, Sanofi Aventis, Pfizer, Janseen, Normaco (Johnson & Johnson), Specialty Chemicals, Nippon Soda during her working with various companies. This success was due to a International exposure and her trainings by Corporate Quality Compliance Services in ‘Certified auditors course’ ,validation,cGMP,GLP etc.

She has visited National and International suppliers and developed Suppliers of Packaging Materials, Contract Manufactures .

She masters in Technology Transfer, Validations, Factory Acceptance Test for high speed Liquid filling m/c from Canada ,Facility design, Up-Gradation because of her trainings from Well known Raytheon Agency ,USA & Documentation as per USFDA/Local Regulatory Authorities.

She has also conducted training programs on the above topics at leading Formulations and API manufacturing companies.

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