Microsoft Word - LowLactose_ERP-Proposal-May2019
UJWAL S. PATIL 3114 Banks Street, New Orleans, LA 70119 (504) 919-3275 (C) ujwalpatil@eurofinus.com www.linkedin.com/in/patilu SUMMARY Cross-disciplinary, bio-analytical chemist responsible for method development and validation using a broad range of analytical techniques. EDUCATION MS, PhD in Analytical Chemistry, University of New Orleans, New Orleans, LA (2010-2015) Dissertation: Development of magnetically separable live cell surface labeling reagents for structural profiling of solvent exposed cell surface proteins. Advisor: Dr. Matthew Tarr, GPA: 3.4/4.0 MS in Pharmaceutical Sciences, Idaho State University, Pocatello, ID (2008-2010) Thesis: Study of anticancer and anti-microbial properties of Blood vine plant obtained from Guatemala. Advisor: Dr. James Bigelow, GPA: 3.83/4.0 Bachelor of Pharmacy , Amravati University, India, (2003-2007), GPA: 3.97/4.0 Developed and validated analytical testing methods to quantify veterinary drugs, mycotoxins, industrial contaminants, and proteins in a variety of complex food matrices. Developed sample preparation strategies for extraction of a variety of food contaminants from complex food matrices Developed extraction methods which utilized immunoaffinity based enrichment, and hydrophilic lipophilic extraction Performed analytical validation studies using UHPLC-MS/MS (AB Sciex 4000, 5500, 6500 Triple Quad/QTrap, Agilent 6470 and 6495), UPLC/HPLC-UV/FLD (Agilent 1260 infinity, Shimadzu Nexera and Prominence) to provide data in support of proposed analytical method. Trained operational managers and analysts for new methods developed. Selected and purchased UPLC and LC-MS/MS instruments Participated in Scientific Communities to stay current with analytical technology. RESEARCH EXPERIENCE Method development Scientist, Eurofins Central Analytical Laboratories 2015-present
Interim Manager, Veterinary drugs and Mycotoxins, Eurofins Central Analytical Laboratories June2018-Sepember 2018
Responsible for direct line supervision of analysts and all activities relating to sample testing and instrument maintenance. Training of employees on test methods, safety rules and procedures as well as quality program. Data review of all test results and determining if controls meet QC acceptance criteria. Authorizing technical documents including Standard Operating Procedures, and control specifications. Monitoring equipment control documentation, employee's punctuality, work habits, and communication of workers' performance to upper management.
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