I'm working with a small, ambitious sponsor company with a late-stage drug-device combination programme. They need someone to take full ownership of the infusion device, reporting straight to the Chief Solutions Officer.
Design and manufacturing sit with external partners. You're the one holding it all together and making the calls.
What you'll be doing:
- Owning the device programme end to end: plan, budget, risk and decisions
- Holding design and manufacturing partners to scope, and challenging their testing and documentation
- Keeping the design history file and traceability tight
- Delivering device content for US and EU combination product submissions
- Getting verified devices, kits and training materials to trial sites on schedule
- Owning the software side, including SaMD lifecycle and cybersecurity
What you'll need:
- Infusion, injection or fluid delivery device development, through design control to clinical or commercial use
- Small-company experience: broad scope, lean support
- A track record managing external design and manufacturing partners
- Experience supplying devices into interventional clinical trials
- Strong ISO 13485, ISO 14971 and combination product knowledge (US and EU)
- Working knowledge of clinical and commercial builds
Nice to have: IEC 62304 / SaMD, AI-enabled devices, neurological or intraocular delivery, gene or cell therapy.
Regular travel to partner and clinical sites across Europe and the US.
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Medical Device Programme Lead employer: Barrington James
Barrington James is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in Epidemiology and Real-World Evidence. With a strong emphasis on employee growth, we offer tailored development opportunities and the chance to lead impactful projects across diverse therapeutic areas in the dynamic UK/Europe market. Join us to be part of a team that values flexibility, creativity, and meaningful contributions to healthcare advancements.
