Experience

The MetroHealth System (Cleveland, OH)

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Pharmacy Financial and Business Manager

  • Jul 2015 - Present

• Business Analyst

  • Jan 2014 - Jul 2015



Boehringer Ingelheim

• Analytical Reviewer

  • Jun 2011 - Dec 2013

  • Analyze, review and audit wet and analytical chemistry techniques during testing of raw materials, final product, stability samples and components for all phases of the production process • Perform the following wet chemistry tests: pH, titrations, determination of physical appearance, UV, specific gravity• Use and maintain analytical instrumentation such as KF, HPLC, UPLC, IC and GC • Train new chemists on SOP’s, analytical testing techniques, and time-management skills• Investigate and resolve analytical data inconsistencies, including troubleshooting of instrument malfunctions and interpreting aberrant data, assisting with ANDA (Abbreviated New Drug Application) filings and submissions• Conduct regulatory reviews of technical summaries• Manage the Empower Chromatographic Data System including routine maintenance, creation and implementation of an up to date training program, and constant improvement to ensure that all regulatory requirements are met• Review all tests against the specifications, methods and SOP’s to ensure that it could be turned in by usage of the company• Enhance efficiency of laboratory operations through use of Lean Sigma techniques



Boehringer Ingelheim

• Germany
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Control Chemist

  • Jun 2008 - Jun 2011



Mylan Pharmaceuticals ULC

• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Quality Control Chemist/Team Lead

  • Aug 2004 - Nov 2007

  • Supported routine activities of Pharmaceutical Quality Control involving testing intermediates, finished products and raw materials• Performed annual reviews on chemists within team• Trained new chemists on SOP’s and analytical testing techniques, including HPLC• Resolved analytical difficulties including troubleshooting instrument malfunctions, interpreting aberrant data, writing investigation reports and revising Standard Test Methods (STM’s) for clarity and to improve high sample throughput in the QC environment• Provided assistance in the audit of protocols and reports in support of method validation and method comparison• Reviewed method transfer process of Raw Material, in-process, and final product testing and change control of analytical test methods and specifications