Medical Device Consultant Regulatory Affairs
Introduction
Jennifer joined Qserve in October 2022 as a Medical Device Consultant, based in Belgium. She will support medical device manufacturers in projects related to quality and regulatory affairs.
Jennifer about working at Qserve
“I really enjoy working with people from different countries and cultures. This is enriching on both a personal and professional level since we all have different backgrounds and professional experiences. I am happy to be part of Qserve and am eager to expand my knowledge in the regulatory, clinical, and quality areas to serve customers as best as I can. I always knew that my career would be focused on improving patient health.”
Before Qserve
Before working at Qserve, she obtained a BSc degree and an MSc degree in Biomedical Sciences at the Université de Namur (Belgium) with a master’s thesis focused on the consequences of mutants of a lysosomal enzyme on the lysosomal enzyme trafficking and on uterine cancer cell behavior. The degree also involved an internship in Regulatory Affairs where Jennifer gained valuable experience with custom-made devices and 3D printing.
The key expertise areas of Jennifer:
- Medical devices
- Custom-made devices
- 3D printing
- Design and implementation of preclinical studies
- EU MDR
- Regulatory intelligence strategies
- Biocompatibility and ISO 10993 standards
- Languages: French and English