Pam Nieves

Pam Nieves has a wealth of experience in Quality Assurance & Compliance, Quality/EHS Management, Quality Management and Safety Program Development, and Internal/External Auditing. Pam began their career in 1997 as a QA/QC Scientist at Penwest Pharmaceuticals, where they approved and released raw, in-process and finished product materials and performed annual product reviews. In 2003, they held two positions simultaneously, Environmental, Health & Safety Manager at Genzyme and Quality Manager at Genzyme Genetics. In this role, they implemented comprehensive Health and Safety and Environmental Management Systems, and maintained compliant Quality Systems. From 2007 to 2010, they worked as a Sr. Regulatory Specialist at Penwest and an Independent Quality & Safety Consultant/Internal Auditor. From 2011 to 2015, they were a Quality, Safety and Regulatory Manager, Laboratory Quality Consultant at Histopathology Services, LLC, where they directed and managed all Quality, Safety, Regulatory activities and collaborated with multiple state and regulating agencies for compliance. From 2015 to 2017, they were a Sr. Quality Assurance Manager at Berkshire Sterile Manufacturing, where they were a Senior Management Member, reported directly to the CEO, and grew the QA team from 1 to 7. Finally, from 2017 to 2019, they worked as a Quality/EHS Manager at ProAmpac and an Associate Director and Sr. Manager of Quality Assurance & Compliance at Trevi Therapeutics, Inc.

Pam Nieves attended Marist College from 1989 to 1991, studying Computer Science. Pam then transferred to Western CT State University and earned a BA in Biology with a minor in Chemistry in 1993.