
Priyanka Pathak
Summary: Eight plus years of experience with Masters of Science (M.S.) in Industrial Pharmacy with experience in Analytical Method... | Washington DC-Baltimore Area, Washington DC-Baltimore Area, United States
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Priyanka Pathak’s Emails pr****@va****.com
Priyanka Pathak’s Phone Numbers No phone number available.
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Priyanka Pathak’s Location Washington DC-Baltimore Area, Washington DC-Baltimore Area, United States
Priyanka Pathak’s Expertise Summary: Eight plus years of experience with Masters of Science (M.S.) in Industrial Pharmacy with experience in Analytical Method Validation, Analytical Quality Control (QC), Quality Assurance (QA) and pharmacovigilance. Awareness regarding current Good Manufacturing Practice (cGMP), Current Good Laboratory Practices (cGLP), International Conference on Harmonization (ICH) guidelines and 21 CFR Part 11. Sound knowledge of production process in the area of solid, semi-solid and liquid dosage form. Understanding of SOP development, non-conformance/CAPA and other documentation management systems. Good understanding Familiar with Spontaneous post-marketing surveillance with respect to drug safety. Able to work independently and a good team player with good written and communication skills. Ability to follow SOP and execute the given task accurately and solve problems with creativity. Skills: Analytical Instrument Skills: Dissolution Apparatus, HPLC, TLC, UPLC, Infrared and UV-VIS Spectroscopy, Friability tester, Hardness tester, Disintegration, Karl Fischer Titrations, pH meter, Titration, Density Meter, Torque Tester. Software Skills: SAP, Empower, LIMS TotalChrom, ARGUS Safety, Sebel Data Analysis, Microsoft (Word, Excel, PowerPoint) LEGAL STATUS IN USA: H-1B (Requires Sponsorship)
Priyanka Pathak’s Current Industry Vanda Pharmaceuticals
Priyanka
Pathak’s Prior Industry
Cognizant Technology Solutions
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Kabco Pharmaceuticals
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Revereit
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Lupin Pharmaceuticals
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Pii
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Vanda Pharmaceuticals
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Work Experience

Vanda Pharmaceuticals
Manager QA / CMC Regulatory
Wed Sep 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Pii
Quality Control Project Lead
Tue Oct 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Sep 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Pii
Sr. Chemist
Sat Sep 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Nov 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Lupin Pharmaceuticals
Standard Coordinator/Quality Control Chemist-III
Mon Aug 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Aug 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Lupin Pharmaceuticals
Analytical Stability Chemist-II
Mon Jun 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Aug 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Lupin Pharmaceuticals
Method Validation Chemist-I
Tue Apr 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jun 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)
Revereit
Validation Trainee
Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Apr 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Kabco Pharmaceuticals
Laboratory Technician
Mon Jul 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Cognizant Technology Solutions
Data Analyst for Pfizer Project
Tue Feb 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jul 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)