Pulkit Parikh

Background

About Pulkit Parikh

I am Pulkit Parikh (M.Pharma in QA) having cumulative more than 13 years of pharmaceutical industrial exposure (Injectables) currently working as a Senior Associate at Baxter Pharmaceuticals India Private Limited, Ahmedabad in QMS department since Apr-2022, to ensure effective and timely closure of the QMS elements. Earlier, I have worked with Liva Pharmaceuticals, Mylan Lab.(Ahmedabad), Intas Pharmaceuticals,Baxter and Nirlife Healthcare. My overall portfolios consists working in various sub-division of Quality Assurance viz. include Documentation, In-Process QA, Validation and QMS and production. I have been particularly interested in learning the regulatory aspects which will improve my pharmaceutical knowledge and now wishes to develop my career by working in QMS, Audit / Regulatory compliance, QA-RA departments. I would welcome the chance to work as a member of a dynamic team, where I could make a significant contribution while developing my skills yet further I would be happy to show you a portfolio of my work. So if there is any openings in your esteemed organization, which matching to my profile, please make a call or send me a mail for the further communication. Technical Expertise: Handling of QMS (NCR, CAPA, DCR, Change Control, OOS, OOT, OOL, OOA, LIR, CAPA, DCR, Change Control) Elements In-Process Quality Assurance Batch Record Review and Batch Release Handling of Market Complaint Basic knowledge of validation activity Faced USFDA, MHRA, TGA, INVIMA, various Party / Customer Audits