Webinar - The new QMS Normal Post COVID19 for the Pharma, Life Sciences & Medical Device Companies

GMP Auditor

Over nineteen years of experience in Quality and technical operations of pharmaceutical formulations like tablets, liquid dosage, soft gel capsules, capsules, herbal medicine, herbal cosmetics, pharmaceutical APIs and medical device. Skilled in decision making, selection of optimistic approach and negotiation for the implementations of the decision, strong inter personal skill and result oriented and as a Quality Conscious Personality. Well versed with cGMP/GLP regulations for API’s and dosage forms. Hands-on with USFDA, MHRA, TGA, HSA, Gulf FDA and ISO requirements and audits designing, validation, setup, technology transfer and start-up of new pharma facility. Expert in internal, vendor and third party audits in compliance with cGMP and ISO standards.