Posted: 8 June
The role
A Technical Documentation & Development Engineer is required to support medical device product development through robust documentation, CAD formalisation, and regulatory compliance. The role focuses on ensuring all new and legacy products meet MDR requirements, with a strong emphasis on technical file ownership, structure, and accuracy. Client Details This is an established healthcare manufacturer operating within a regulated medical device environment, focused on improving patient outcomes through product innovation and continuous improvement. The business has a growing portfolio of products and is investing in strengthening its documentation, compliance, and development processes. Description Key responsibilities: Produce and maintain technical documentation in line with MDR requirements Build, manage, and update Technical Files for both new and legacy products Take ownership of legacy documentation, including reverse engineering and generating CAD models/drawings Create production-ready, revision-controlled CAD drawings from existing products and development inputs Document all design changes, improvements, and development activities Ensure compliance with medical device regulations, standards, and internal gated processes Support risk management activities and maintain structured design documentation (e.g. DHF) Collaborate with cross-functional teams (R&D, Manufacturing, Regulatory, Supply Chain, Sales) Support value engi...
