Meghal Patel
Qc Analytical Chemist-i @Medical Products Laboratories, Inc
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WORK HISTORY
Qc Analytical Chemist-i @Medical Products Laboratories, Inc
Philadelphia, PA, US
Analysis (Impurity, Assay, Identification, Purity) of Raw/Bulk materials, Finished products and Stability samples by GC/MS, HPLC, LC/MS, UV, FTIR, DSC, TGP and other Spectroscopy lab techniques• Analytical Method Validation and Development as per regulatory guidance (ICH, FDA, USP, BP, EP etc.) for new formulations, including Tablets, Capsules, Gels, Pastes, Creams and Oral solutions/Suspensions• Reviewing of the analytical data, Preparing CoA-Specification (Raw materials, Bulk-Finished Products)• Performing method transfer activity with various customers and handling regulatory affairs• Performing various analytical tests to ensure the quality of the product• Calibration of various analytical instruments (HPLC, LC/MS, GC/MS, FT-IR Spectrometer, Refractometer, Viscometer, UV-Vis Spectroscopy, pH, Coulometric/Volumetric Titration, Dissolution Apparatus etc.)• Pharmaceutical experience in Quality control and Analytical Development, fully versed in cGMP, cGLP, FDA, ICH and other regulatory agency requirements sufficient to comply with quality operation and compliance
EDUCATION
CHAROTAR UNIVERSITY OF SCIENCE AND TECHNOLOGY
Master of Pharmacy, Pharmaceutical Technology, First Class with Distinction-3.5 GPA (WES)
Entrepreneurship Development Institute of India
Biotechnopreneur Programme, Entrepreneurship/Entrepreneurial Studies, Certification Programme
Gujarat Technological University, Ahmedbabd
Bachelor of Pharmacy, Pharmacy, First Class-2.85 GPA (WES)
Duke University - The Fuqua School of Business
Product Managment Programme-Duke Corporate Eduction, Business Administration and Management, Certification Programme
ABOUT MEGHAL PATEL
I am a skilled and experienced research fellow, backed by a solid academic background and exceptional communication abilities. My expertise lies in the pharmaceuticals industry, specifically in areas such as Oncology, Nanotechnology, Cell Culture – Aseptic Techniques, cGMP, GLPs, Analytical Techniques (HPLC, LC/MS, GC/MS), API Validation, SoPs, Formulation Stability, DMFs, ICH, Pre-Clinical Study, Drug Regulatory Affairs, Intellectual Property Rights (IPR), Product Management, and Quality by Design (QbD) through Design of Experiment (DOE) approach. My objective is to make a meaningful contribution to an organization that values growth and excellence, while also advancing my own career. My approach is characterized by a can-do attitude and a drive for success. I am proactive and take the initiative, and I am open to feedback, using it to improve and adapt as needed. Throughout my research career, I have gained extensive hands-on experience in the use of advanced instruments and managing both client relationships and research teams in the field of pharmaceutical sciences.
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