This is a contract of 1 year as a Consultant. Location : Braine l'Alleud Your Responsibilities: Lead and manage the Clinical Drug Delivery Devices (CDDD) sub-teams for selection and assessment of devices. Provide expert technical support to clinical teams and trial sites on drug delivery devices. Analyze and validate device specifications (e.g., needle size, tubing length, flow rate) to ensure compatibility with drug products. Support technical assessments of devices selected by CROs. Address and process Change Requests from clinical sites (e.g., device availability or new site activation). Act as the subject matter expert (SME) for all device-related queries during clinical trial lifecycles. Ensure timely documentation and updates of device decisions and changes in the CDDD database. Collaborate cross-functionally with QA, RA, Safety, and SME teams to meet trial timelines. Profile We’re Looking For: Must-Haves Master’s degree in a relevant scientific or engineering field (or equivalent experience). 4–8 years of experience with injection systems (syringes, pumps, needles, infusion lines, etc.) in clinical or technical contexts. Strong technical understanding of medical devices and drug-device compatibility. Experience in clinical trials setup and device support. Thorough knowledge of medical device regulations : EU MDR 21 CFR Part 820 ISO 13485 GxP (GMP/GCP) Excellent analytical and problem-solving skills to assess technical specifications and ensure product compatibility. Solid project management and risk management capabilities. Excellent written communication and documentation skills. Strong autonomy, responsiveness, and attention to detail. Nice-to-Haves Experience supporting clinical operations or sites in device selection. Knowledge in QA or regulatory affairs in combination with technical skills. Experience with drug-device compatibility testing and materials of contact assessments.