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.
Essential Skills
- 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
Desirable Skills
- 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.
