SPDS ERP CVs - DEC 2017

CURRICULUM VITAE: GARRETT A. ZIELINSKI

scientific publications and presented the material at domestic and international scientific meetings. He also assisted other functional groups with method development projects as needed. 03/2011 – 08/2012: Technical Leader III, Nutritional Chemistry and Food Safety Mr. Zielinski served as technical leader for carbohydrate analyses conducted within Nutritional Chemistry. Along with all responsibilities listed below as technical leader, he acted as a lead chemist with new methods, method modifications and specific client specific procedures. He regularly assisted clients with interpretation of results and troubleshooting problematic sample analyses. He identified process improvement initiatives and helped drive these projects to completion. Mr. Zielinski also identified commercial development opportunities and helped develop and implement these service offerings. He authored and co-authored scientific papers, presentations and posters that were published and presented at scientific meetings. He also assisted other functional groups as necessary. 02/2010 – 03/2011: Technical Leader II, Nutritional Chemistry and Food Safety Mr. Zielinski served as a Technical Leader for routine analyses under the direction of Nutritional Chemistry management. His overall responsibility was the technical conduct of the fiber and sugar related assays, study work, and validation procedures, as well as the analytical direction, review, documentation and reporting of results. 09/2009 – 02/2010: Research Associate I, Pharmaceutical Analysis Mr. Zielinski served as lead chemist on projects, helping drive the project from initiation to completion. He provided input and participated in project meetings, plans, and guided project work. In concert with the PI, he developed Protocols for method transfers/validations and discussed study designs/results with clients. Mr. Zielinski performed method development/validation of various analytes in a variety of matrices. He performed complex analyses using unfamiliar or new methods. He suggested and performed modifications to test methods and procedures when appropriate. Mr. Zielinski wrote, revised, and reviewed methods, SOPs, and portions of reports and protocols. He assisted with Quality Audit responses and CAPAs as assigned. 06/2008 – 09/2009: Research Assistant III/Team Leader, Pharmaceutical Analysis Mr. Zielinski served as a project leader for a team of five chemists. He was responsible for scheduling work and ensuring this work is completed efficiently, on-time and with the highest quality. He was the team’s contact for technical and lab issues that arise. He was also the team contact for the Principle Investigator with lab-based questions and concerns. In concert with the PI, he developed Protocols for method transfers/validations and discusses study designs/results with clients. Mr. Zielinski assists with Quality Audit responses and CAPAs as assigned. He was constantly striving for process improvements and participates in process improvement initiatives. Mr. Zielinski performed method Mr. Zielinski implemented analytical methods from the United States Pharmacopoeia (USP), client protocols, or other sources in accordance with standard operating procedures (SOPs), GLP and cGMP regulations. He performed routine and nonroutine assays in support of GLP and cGMP – related studies for multiple customers. He was experienced in HPLC, GC, IC, dissolution testing and UV- Spectrophotometer analysis, and helps train new employees on these analyses. Mr. Zielinski also reviewed and evaluated analytical methods and results to assure scientific expectations and regulatory guidelines are met. He was proficient in Chemstation, Empower, and Nautilus. He also participated in client visits/communications and presented study results directly to clients. development/validation of various analytes in a variety of matrices. 07/2007 – 06/2008: Research Assistant II, Pharmaceutical Analysis

NA-GEN Form Number 79

Revised: 30 Dec 2011

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