Richèle joined Progress in May 2015. Before that she worked as a QA consultant and project manager in various Quality positions within Pharmaceutical companies. She is experienced with FDA inspections, QA and GMP trainings, Deviation and Change management, Product scale-up, Pharmaceutical development (CMC), product and process Tech Transfer, System Validation, Audits of logistical warehousing, Data integrity remediation, Serialization/aggregation projects and Quality management systems.

Richèle has 15+ years of experience in the pharmaceutical and biotech industry. She holds a Bachelor’s degree in Molecular Biology and Microbiology. Richèle started her career as a technician in a research laboratory and from 2008 to 2015 she worked in aseptic and inhalation capsule production as quality systems and QA validation expert.