Annick boasts over 15 years of extensive expertise in the fields of ethylene oxide sterilization, quality management, and pharmaceutical manufacturing. In her role as Technical Director, Chemical sterilization Pharma, Annick leads the Ethylene Oxide (EO) sterilization projects at numerous Sterigenics facilities and supports the sites as the technical expert with pharmaceutical project responsibility. She’s also supporting the development and validation of new technologies like NO2. Renowned for her seasoned speaking engagements, Annick is a frequent presenter at significant industry conferences such as CPhI, and she holds acclaim as a recognized trainer by the Parenteral Drug Association (PDA). Her contributions extend beyond the podium, as she has also contributed to various technical journals. Annick’s presentations consistently delve into innovative and tailored solutions for the terminal sterilization of pharmaceuticals. Recognizing the evolving landscape of pharmaceutical regulations, Annick has recently augmented her skill set by acquiring competencies in Regulatory Affairs.
Education: B.Sc. Liège (Belgium), DES Total Quality from Faculté Polytechnique Mons (Belgium), Management of Pharmaceutical Quality Systems from the ECA Academy, Regulatory Affairs certificate Liège-Namur University
Certifications: Certified Trainer, EO Sterilization Validation, Quality auditor
Expertise: EO and NO2 Sterilization Validation of Medical Devices and Pharma Applications (API, drug products, Prefilled devices), Cycle Design and Development, EO Residues, Quality management systems, Regulatory Affairs of health care products
