Richèle joined Progress-PME in May 2015. For Progress-PME, she has worked as QA consultant and project manager in various Quality positions within Pharmaceutical companies affiliated 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’ experience in the pharmaceutical and biotech industry. She holds a Bachelor’s degree in Molecular Biology and Microbiology. Richèle started her career as technician in a research laboratory and from 2008 to 2015 worked in aseptic and inhalation capsule production as quality systems and QA validation expert.
Since October 2016, Richèle is attending the Qualified Person and Professional Development training program (NSF England/University of Strathclyde) for a MSc in Pharmaceutical Quality and GMP with the aim to obtain QP registration.
Richèle (1976) enjoys going out, travelling, having a cup of coffee or a drink with friends, and sports. Her favourite sports are skiing, tennis and yoga.
- QA and validation support and GMP consultancy
- QA management
- GMP / QA training
- Project coordination and management
- Quality Risk management
- CSV and Data Integrity
- Aseptic production