Technical Documentation and Development Engineer

A Technical Documentation and 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 DetailsThis 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.DescriptionKey responsibilities: Produce and maintain technical documentation in line with MDR requirementsBuild, manage, and update Technical Files for both new and legacy productsTake ownership of legacy documentation, including reverse engineering and generating CAD models/drawingsCreate production-ready, revision-controlled CAD drawings from existing products and development inputsDocument all design changes, improvements, and development activitiesEnsure compliance with medical device regulations, standards, and internal gated processesSupport risk management activities and maintain structured design documentation (e.g. DHF)Collaborate with cross-functional teams (RandD, Manufacturing, Regulatory, Supply Chain, Sales)Support value engineering initiatives to improve cost efficiency without ..... full job details .....