Medical Technology Jobs in Exeter

Johnson & Johnson MedTech · Spring House, United States · US$102,000 – US$177,100 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors performing anonymisation and synthetisation, serves as the primary contact for YODA Project requests, and supports external research teams using clinical study data. Operates independently as a subject matter expert within the Clinical Data Standards and Transparency team.

Johnson & Johnson MedTech · Beerse, Belgium · €79,800 – €137,770 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, securing clinical team approvals. Supports external research teams using clinical study data.

Smith & Nephew · UK - Field

Designs and delivers medical education programmes on Advanced Wound Management across the Nordics, UK & Ireland and Canada, working with healthcare professionals, clinical experts and professional societies. Blends in-person and digital learning, manages programme logistics and outcomes, and collaborates with Medical Education, Marketing, Professional Affairs and Commercial teams. Field-based with extensive travel (up to 70%).

Newton Colmore · Cambridge

Provide regulatory support across a Cambridge product development business, guiding multidisciplinary engineering and science teams on compliance with ISO 9001, ISO 13485 and FDA 21 CFR 820. Monitor international regulatory changes, support external audits and contribute to quality management system improvements across medical and non-medical projects.

GlobalData Plc · Birmingham

Acts as the bridge between pharma consulting teams, the wider business and developers on an AI-enabled competitive intelligence platform running on AWS with Python, PostgreSQL and React. Gathers requirements, maps processes, manages the backlog, coordinates UAT and onboarding, and builds business cases with cost/benefit analysis and value tracking.

GlobalData Plc · Birmingham

Builds and runs an AI-enabled competitive intelligence platform for the pharmaceutical market, working end to end from PostgreSQL and Python APIs through to React and TypeScript interfaces. Sits in a small Birmingham-based team, developing data-rich workflows for consulting users and gathering their feedback directly.

GE HealthCare · London

Provides enterprise leadership across strategic business portfolios, acting as senior integrator for innovation execution and technology interface for Product Leaders. Leads NPI reviews, owns portfolio performance and ROI realisation, governs investment decisions, and assesses build-versus-partner opportunities across CTO, Medical and Regulatory functions.

Newton Colmore · Cambridge

Provide regulatory support across a product development organisation, working with engineers and scientists to align projects with global requirements. Maintain and improve the QMS, apply ISO 9001, ISO 13485 and FDA 21 CFR 820, monitor regulatory changes, and support external audits.

Yolk Recruitment · Bridgwater · £55,000 pa

Owns quality operations across a precision manufacturing site, maintaining QMS, certifications and audit readiness while leading continuous improvement. Acts as main contact for customers, auditors and suppliers, managing non-conformances, root cause investigations and corrective actions using SPC, PFMEA, PPAP and 8D. Also supports day-to-day Health & Safety activities alongside Production and Engineering teams.

Healthium Clinics · Henley-on-Thames · £35,000 pa

Supports market access, quality systems and governance across healthcare and technology activity, coordinating evidence packs, tenders and regulatory documentation. Maintains the Quality Management System, risk registers and audit actions, and monitors MHRA, CQC, NICE and ICO requirements. Works with clinical, technical and commercial colleagues to keep registrations and controls inspection-ready.

Sue Ross Recruitment Ltd · Sheffield · £32,000 pa

This role involves driving sales of medical devices through a consultative, virtual-first approach, combining clinical and technical expertise with strong account management. The candidate will identify customer needs, deliver product solutions, and develop strategic business plans to grow both existing and new accounts. Success requires analytical insight, proactive market awareness, and effective communication across video, phone, and in-person channels.

HCRG Care Group · Runcorn · £50,000 pa

Leads end-to-end data migration projects moving sensitive patient records between Electronic Patient Record systems, coordinating internal teams, external organisations and suppliers. Combines technical project management with data quality, information governance and clinical safety, working closely with the Head of Clinical Systems. Predominantly remote with occasional UK travel.

Medtronic · London · £77,040 – £115,560 pa

Serves as a senior scientific expert for the Neuromodulation & Pelvic Health portfolio, leading external scientific engagement with KOLs, healthcare professionals and medical societies across Western Europe. Delivers evidence-based clinical information, runs advisory boards, CME programmes and congress activities, and partners with clinical, regulatory and commercial teams on medical affairs strategy. Remote UK-based role with frequent travel.

Automated Industrial Robotics · Wakefield

Designs special purpose machinery from concept through to production-ready drawings, working with AutoCAD 2D/3D and pneumatic and electrical components. Manages schedules, budgets and scope changes while liaising with the Technical Director and section leads, and conducts machinery risk assessments and detail checks on colleagues' work.

Randstad Construction & Property · London

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships to deliver Patient Cloud projects on time and within budget. Involves risk assessment, study documentation, and meetings, with expertise in eCOA/ePRO, eConsent, virtual trials or wearables. Fully remote, but requires flexibility to work American time.