Dr. Rajesh Kaushik

A quality consultant and qualified auditor with 20 years of experience in Pharmaceutical Manufacturing Organizations, with wide experience in handling various disciplines: :Quality Assurance ,Quality Control, Training and Development, Analytical R&D and Audits. Have represented the companies in regulatory inspections; USFDA, MHRA, PMDA, TGA, CDSCO, WHO-Geneva, EU-GMP, MFDS Korea and other reputed customers. Performed more than 225 audits of manufacturing units of drug products (OSD, Injectables, Ointment, Liquids), APIs, KSMs, Medical Devices, Biologicals.

Qualification as a Lead Auditor:
> Certified Lead Auditor from IRCA, UK (Certificate Number : 6056410)
> Qualified Auditor of Intertek, France
> Qualified Auditor by AFA, Spain
> Qualified Auditor by Chemsquare (Qualifyze now), Germany
> Qualifified as Auditor is under process by PQE, Italy
> Qualified Technical Expert (For Pharmaceuticals) by BSI
> Qualified consultant (Auditor and trainer) of Eurofins, France

Working Experience:
> Worked in Pharmaceutical Industry for 15 years in Manufacturing, Quality Control, Analytical Research and Development, Regulatory Affairs, IPR (Intellectual Property Rights) and Quality Assurance.
> Working as a freelancer qualified Lead auditor and GMP consultant for past six years.