QbD Group
Lode van Aert is a Validation Engineer at Organon Heist since June 2020, focusing on coordinating the installation and qualification of utility equipment, as well as developing and executing commissioning and qualification protocols and reports. Prior to this, Lode served as a Life Science Consultant at QbD, providing support to life sciences companies worldwide from product conception to patient delivery. Lode's experience also includes roles as Project Coordinator for Serialization at Sharp Packaging Solutions, where project coordination and stakeholder communication were key responsibilities, and as Production Manager and Process Engineer at AUTAJON LABELS Belgium, emphasizing workflow analysis and ERP system utilization. Lode holds a Master of Science degree in Biowetenschappen: voedingsindustrie from KU Leuven and has experience in optimizing production lines through internships in industrial engineering and lean manufacturing.
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.