Medical Technology Jobs in Exeter

SRG · Lancashire

Maintains and improves a medical device Quality Management System in line with ISO 13485 and FDA QSR, leading non-conformance, deviation, complaint and CAPA investigations with root cause analysis. Supports internal, supplier and regulatory audits, risk management under ISO 14971, validation and design transfer, working with Manufacturing, R&D, Regulatory Affairs and Supply Chain.

Johnson & Johnson MedTech · Raritan, 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 · Titusville, 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, and serves as the primary contact for YODA Project requests, supporting 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.

Medtronic · London · £76,800 – £115,200 pa

Supports software quality across the full product development lifecycle in Medtronic's surgical operating unit, from requirements and design through verification, validation, release and post-market support. Involves risk management (SFMEA, hazard analysis), design reviews, traceability documentation, CAPA and audit readiness, working closely with software, systems, regulatory and quality teams.

OrganOx · Oxford

Leads a team of Windows software engineers building device-hosted applications and services for Class II and III medical devices, covering GUI development, connectivity and cybersecurity mitigations. Owns the full SDLC, regulatory compliance (FDA, ISO 13485, IEC 62304), roadmaps, budgets and hiring, while acting as technical representative to regulators, partners and customers.

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.

Ripple · Luton · £65,000 pa

Hands-on operational leadership across manufacturing, quality assurance, supply chain, purchasing and facilities at a medical equipment manufacturer. Sits on the Senior Leadership Team, owning site health and safety, ISO compliance and continuous improvement, while partnering with executive leadership on business planning and representing the site at group forums.

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.