Pearl Pathways announces the hiring of Eric English as a Quality Assurance and Regulatory Affairs (QA/RA) Advisor. Eric brings over 18 years of experience in quality, regulatory, and auditing roles within the pharmaceutical and medical device industries, including over a decade of direct consulting experience.

Eric English, MS, CQA, RAC

An accomplished quality and regulatory affairs professional, Eric’s previous experience includes developing, implementing, and managing GMP quality systems for pharmaceutical startups, leading the external audit program for one of the world’s largest contract research organizations (CROs). He was also responsible for creating and managing the quality and compliance infrastructure for a biotech CDMO/CTO which was performing early phase cell culture and protein purification, GMP cell banking, and tissue-based therapy development and testing.

Eric is a BSI Accredited ISO 13485:2016 Lead Auditor, holds a Regulatory Affair Certification (RAC) from the Regulatory Affairs Professionals Society (RAPS) (2009) and is an ASQ Certified Quality Auditor Certification (CQA) (2011).  Eric has a BS in Chemistry from Haverford College and an MS in Biotechnology from Johns Hopkins University. Learn more about Eric by viewing his full biography.