A global medical device company working on a new product launch is seeking an experienced Medical Device Engineer to support on a 6-month contract basis, starting as soon as possible.

You'll work with a cross-functional development team across the UK and US to support late-stage product development and launch readiness. The role will focus on Design History File documentation, marketing claims, supporting evidence summaries, and process documentation for a medical device system with both device and instrument elements.

Aside from initial onboarding at a UK site, the role will be predominantly remote.

• Medical device product development experience
• Design History File/DHF documentation experience
• MDR and FDA 510(k) knowledge
• Technical writing and evidence summary creation
• Cross-functional communication with engineering, regulatory, clinical, and marketing teams

• Experience with implantable devices, surgical instruments, or complex medical device systems
• Experience creating marketing claims, launch documentation, or procedural documentation

This is a strong fit for engineers who are confident owning design documentation, pulling together compliant evidence, and working with global teams to support late-stage medical device launch activity.

Please visit our website to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement.

To find out more about Real, please visit our website

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC387148 England and Wales