Harshit Patel
About Harshit Patel
Harshit Patel is a System and Equipment Validation Engineer at Bristol Myers Squibb in Warren, New Jersey, with extensive experience in pharmaceutical quality assurance and production.
Current Title at Bristol Myers Squibb
Harshit Patel holds the position of System and Equipment Validation Engineer at Bristol Myers Squibb in Warren, New Jersey, United States. His role involves handling and validating complex GxP equipment and computer systems. He develops critical documents such as Validation Plans, Risk Assessments, SOPs, URSs, IQs, OQs, PQ/UATs, CS and DQs, RTMs, and Validation Summary Reports.
Previous Role at Amneal Pharmaceuticals
Between 2016 and 2019, Harshit Patel served as a Quality Assurance Inspector III at Amneal Pharmaceuticals in New Jersey. During this three-year period, he conducted quality inspections and ensured compliance with necessary standards in pharmaceutical production.
Experience with Various Pharmaceutical Companies
Harshit Patel has a robust background in the pharmaceutical industry, having worked at several companies. These include Global Medicine and Surgical Instruments as a Pharmacy specialist, Unimed Technologies (a division of Sun Pharmaceuticals) as a Production Officer of Parenteral Products, and Relax Biotech Pvt. Ltd. as a QC Control Chemist III. His varied roles in these organizations have provided him with extensive knowledge and hands-on experience in pharmaceutical production and quality control.
Educational Background in Pharmacy
Harshit Patel completed his education at the R.C. Patel Institute of Pharmaceutical Education and Research, where he studied Pharmacy and earned a Bachelor of Pharmacy degree. His educational journey spanned from 2007 to 2011, providing him with a strong foundation in pharmaceutical sciences.
Skills and Technical Proficiency
Harshit Patel is proficient in using a wide range of analytical instruments and software tools. These include HPLC, Dissolution Test Apparatus, UV Spectroscopy, and FTIR for analytical purposes. He is also skilled in utilizing quality and compliance software such as QUMAS, eQRMS, Veeva Vault, Infinity, Blue Mountain RAM, ComplianceWire, JD Edwards, MS Office, MS Project, and Outlook. His expertise extends to handling pharmaceutical production equipment, including DHS, Autoclave, Ampoule and Vial Tunnel, Vial Filling and Sealing Machine, Fluid Bed Dryer, Freeze Dryer, and BFS Machine.