QbD Group
Jens Vandormael has extensive experience in business development within the pharmaceutical sector, currently serving as a Senior Business Development Manager at QbD Group since September 2017, after holding various related positions including Business Development Manager and Project Consultant. Additionally, Jens is an active member of the ISPE Belgium Affiliate emerging leaders board since April 2022, contributing to advancements in pharmaceutical engineering. Prior to these roles, Jens was involved as a Tutor at Sagio.be VZW and as a Master Thesis Student at KU Leuven, focusing on the development of an optical fibre surface plasmon resonance method for monitoring the solubility of aptamer-based medicines. Jens was also a board member of LBK, a student association dedicated to education, during 2016-2017. Educational background includes a degree from KU Leuven, completed in 2017.
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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.