R&D Quality Project Manager | Medical Devices | Dijon, FranceI’m currently supporting an innovative medical device company as they look to strengthen their R&D Quality function.This role sits at the intersection of Quality, R&D, and Regulatory, with a strong project-management focus. You’ll be responsible for ensuring product development activities comply with EU MDR, ISO 13485, and internal design control processes, while working closely with engineering, production, and QA/RA teams.️ Key responsibilities include:Leading R&D Quality projects from planning through execution and reportingActing as the quality reference for design control and development methodologyCoordinating and contributing to technical documentation, including DHF and DMRSupporting product registration and interactions with Notified BodiesReviewing R&D protocols and reports (pre-clinical, clinical, usability)Supporting QMS processes, document control, risk management, and change controlManaging non-conformances and CAPA activitiesParticipating in internal and external audits Profile they’re looking for:Engineering or scientific degree (Quality, Biomedical, Mechanical, or similar)3+ years’ experience in Quality within the medical device industry (or significant equivalent experience)Strong knowledge of ISO 13485, EU MDR (2017/745), and design controlsExperience working in project mode within R&D environmentsComfortable collaborating cross-functionallyFluent English and French is required What’s on offer:A hands-on, impactful role within a growing MedTech environmentClose collaboration with R&D and leadership teamsLong-term opportunity with real ownership and visibilityIf you’re open to a confidential discussion to learn more, feel free to message me directly or apply here and I’ll be in touch.