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.