QbD Group
Laurien Vleeschouwers is an experienced professional in the field of process validation and quality assurance, currently serving as an MSAT Process and Cleaning Validation Engineer at QbD, supporting the MES next-gen project and handling process and cleaning validation activities since June 2022. Prior to this role, Laurien held positions as an MSAT Process Validation Engineer and QA Operations Specialist at The Estée Lauder Companies Inc. and The Janssen Pharmaceutical Companies of Johnson & Johnson, respectively, and has contributed to research and development as an R&D Scientist Compounding and Associate Scientist in Dissolution Sciences. Laurien earned a Master of Science in Biomedical Sciences from KU Leuven, following a Bachelor of Science in the same field, highlighting a strong educational foundation in biomedical basic and translational research.
This person is not in the org chart
This person is not in any offices
QbD Group
The QbD Group supports life science companies worldwide throughout the entire product lifecycle – from idea to patient. We are a multinational company with over 450 high-qualified employees. Our experienced team serves the wider life science industry, with a strong focus on ATMPs, medical devices, IVDs, and digital health, thanks to the specific expertise we have built in these areas. The services we offer fall under the following divisions: • Regulatory Affairs: We help our clients in their journey throughout the entire drug and medical device regulatory lifecycle. • Clinical: We are an expert clinical solutions provider specialized in medical devices and biotech, offering global CRO services and consultancy. • Qualification and Validation: We guarantee that products meet quality demands and comply with regulation through the qualification and validation of your processes, equipment, and software. • Quality Assurance: We offer the full range of QA services necessary to get your product to market in a safe and compliant way, including auditing from certified auditors, setting up your QMS, and all QP (Qualified Person) activities. • Quality Control: Our QC division consists of a GMP laboratory that offers analytical services for testing pharmaceutical raw materials, excipients, and release testing of finished products. • Software solutions: Cloud-based and pre-validated Quality Management Software built for the life sciences, as well as eIFU services which enable IVD and MD manufacturers to digitalize paper Instructions For Use (IFU). • Go to market: We help you launch your product to market by providing marketing and communication services, business development support and sales strategy.