End-to-End Medical Device Programme Lead

Barrington James

Greater London

On-site

GBP 90,000 - 130,000

Full time

22 hours ago
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Job summary

Barrington James is seeking a Medical Device Programme Lead for a late-stage drug-device combination programme in the UK. This hands-on, senior role requires ownership of timelines, risk decisions and end-to-end delivery, with close collaboration across clinical, regulatory, quality, manufacturing, procurement and finance teams.

You will review technical documentation, manage external design/manufacturing partners, and lead regulatory submissions while maintaining device quality and supply

Qualifications

  • Experience leading medical device programmes within a sponsor, with broad ownership and limited internal support.

Responsibilities

  • Own the medical device programme across timelines, risks, decisions and delivery.
  • Manage external design and manufacturing partners, holding them accountable for deliverables.
  • Review and challenge technical documentation, protocols, reports and risk analyses.
  • Manage device development alongside clinical and regulatory timelines.
  • Oversee builds, yields, component lead times, ordering and clinical supply.
  • Own the device budget alongside Procurement and Finance.
  • Support combination product submissions and regulatory responses.
  • Ensure devices, kits, labelling and shipping are ready for clinical sites.

Skills

Programme leadership
Medical devices
Regulatory understanding
Vendor management
Clinical trials

Education

Engineering degree
Life sciences degree

Tools

Design controls

Job description

Barrington James is seeking a Medical Device Programme Lead for a late-stage drug-device combination programme in the UK. This hands-on, senior role requires ownership of timelines, risk decisions and end-to-end delivery, with close collaboration across clinical, regulatory, quality, manufacturing, procurement and finance teams.

You will review technical documentation, manage external design/manufacturing partners, and lead regulatory submissions while maintaining device quality and supply

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