Thomas Polsinelli

Thomas Polsinelli: Email & Phone Number

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Quality Assurance and Operations Consultant at Thomas Polsinelli LLC|Apex, North Carolina, United States

Position:

Quality Assurance and Operations Consultant at Thomas Polsinelli LLC

Location:

Apex, North Carolina, United States

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Last updated: 2025-12-17
Updated: 2025-12-17

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Work Experience 39 years

Quality Assurance and Operations Consultant at Thomas Polsinelli LLC

Jan 2017 - Current

Operations Manager, Commercial Manufacturing at Catalent

Jan 2016 - Jan 2017

Clinical Trial Manufacturing Manager at Catalent

Apr 2013 - Jan 2016

Manufacturing Manager at Catalent

May 2010 - Apr 2013

Senior Director, Manufacturing at Dey Pharma LP/ Mylan

Apr 2004 - Mar 2010

Senior Manager of Manufacturing/Director at AstraZeneca

Sep 1997 - Apr 2004

Manufacturing Supervisor at Astra USA

Jun 1994 - Sep 1997

Manufacturing Supervisor at Synergen

Feb 1992 - Jun 1994

Production Technician at Medi+Physics

Jan 1987 - Jan 1992

Thomas Polsinelli started working in 1987, then the employee has changed 6 companies and 7 jobs. On average, Thomas Polsinelli works for one company for 4 years 5 months.

Their professional focus is 5S, 21 CFR Part 11, and Aseptic Processing across 3 core areas.

Education

Bachelor of Science at Indiana University Bloomington

Master of Business Administration - MBA at Boston College Carroll School of Management

Skills

Compliance, Change Control, Corrective and Preventive Action (CAPA), Laboratory Information Management System (LIMS), SOP, Negotiation, cGMP, 5S, Cleaning Validation, LIMS, Continuous Improvement, Sterilization, Packaging, Biotechnology, Pharmaceuticals, Pharmaceutical Industry, Quality Assurance, CAPA, U.S. Food and Drug Administration (FDA), Process Improvement, Six Sigma, Cross-functional Team Leadership, GMP, Lean Manufacturing, Operations Management, Aseptic Processing, Manufacturing, Operational Excellence, GxP, Change Management, Standard Operating Procedure (SOP), Validation, Manufacturing Operations, Formulation, Technology Transfer, Quality System, Team Building, GLP, Trackwise, Team Leadership, Verification and Validation (V&V), Business Process Improvement, Good Laboratory Practice (GLP), Auditing, Contract Manufacturing, Lean Sigma, V&V, 21 CFR Part 11, Computer System Validation, FDA

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