Medical Technology Jobs

Johnson & Johnson MedTech · Birmingham

Field-based role covering hospital accounts across the West Midlands, building territory plans and driving catheter utilisation and capital sales in electrophysiology. Involves developing clinical and non-clinical customer relationships, executing EMEA marketing strategies, managing tenders and local pricing, and working alongside sales specialists and technical teams.

Johnson & Johnson MedTech · Blackpool

Accountable technology leader for the DePuy Synthes EMEA Deliver domain, owning the regional logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances multi-year transformation delivery with operational reliability, cybersecurity, compliance and lifecycle governance, while leading a team and governing 3PL and vendor technology relationships.

Philips · United Kingdom - Remote Based · £53,410 – £83,930 pa

Leads customer-facing Radiology Informatics programs covering PACS, RIS and enterprise imaging, managing software implementations from order signature through go-live and handover. Runs large cross-functional projects with budgets typically over £1M, handling scope, risk, budget and stakeholder governance. Field-based across the UK, Ireland and Nordics, working from home with around 60% travel to customer sites.

Philips · United Kingdom - Remote Based · £53,410 – £83,930 pa

Leads a team of 20+ clinical consultants delivering Radiology Informatics implementations across the UKI and Nordics, validating solution design against customer clinical needs during presales and guiding C-level stakeholders through sales, implementation and adoption. Coaches the team and sales resources on vuePACS and vueRIS, drives methodology development, and acts as an active member of the European Clinical Consulting community.

Medtronic · London · £44,000 – £66,000 pa

Regional product expert for the ENT/Head & Neck surgical portfolio across Western Europe, driving market development, clinical education and product launches. Partners with surgeons, distributors and sales teams to build adoption and inform strategy, reporting to the Marketing Director in a remote role.

OrganOx · Oxford

Designs mechanical components and assemblies for medical devices using CAD tools, supporting analysis, testing and design verification and validation. Works with manufacturing, suppliers and cross-functional electrical, software and quality teams through the product development lifecycle, preparing documentation to ISO 13485 and participating in risk management and design reviews. Office-based in Oxford with flexibility.

Medtronic · Manchester · £43,200 – £64,800 pa

Field-based role covering the North West, providing clinical and technical support to electrophysiologists, cardiac physiologists and cath lab teams during cardiac ablation procedures using Cryo, PulseSelect and Affera therapies. Involves procedural troubleshooting, product and therapy training, and supporting installations and launches alongside sales and marketing to drive therapy adoption in assigned accounts.

University of Leeds · Leeds · £41,064 – £48,822 pa

Develop a clinically deployable assay for therapeutic drug monitoring of the immunosuppressant tacrolimus, building on a recently created rapid, accurate and low-cost measurement method. Work within a multidisciplinary team focused on in vitro diagnostics assays and devices that improve dosing and patient outcomes, replacing slow mass spectroscopy workflows.

Newton Colmore · Cambridge

Design and develop complex medical devices as part of a multidisciplinary team of mechanical engineers, physicists and electronics engineers. The role is hands-on, spanning CAD, prototyping and functional mechanism design across multiple medical specialisms, including some surgical robotics, with variety rather than a single-device focus.

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.

Pertemps Gloucester · Cheltenham · £25,000 – £27,000 pa

Assembling precision medical devices within a controlled cleanroom, working to GMP standards and ISO procedures to meet production targets. The role involves handling small components with high accuracy in a fast-paced, high-volume environment, with full training provided. It offers a four-day week, Monday to Thursday, with Fridays off.

ACS Staffing Solutions · Malvern · £40,000 – £50,000 pa

Lead the Service and Repairs function for an assistive technology company, combining hands-on electronic fault diagnosis with team leadership and operational improvement. You'll coach technicians, drive root cause investigations with Hardware Engineering, and improve turnaround times and processes while preparing the department for ISO 13485 compliance. The role sits at the intersection of accessibility, technical troubleshooting and quality/regulatory work.

L-ev8 Recruitment Ltd · Burgess Hill · £32,000 – £40,000 pa

Coordinating quality processes, managing non-conformances, supporting investigations and corrective actions, and maintaining ISO 9001 and ISO 13485 compliance. Reporting to the Head of Quality, the role covers document control, CAPA, supplier quality and audit support within a regulated packaging business, with scope to broaden experience across auditing and regulatory compliance.

Fortis Recruitment · Warwick · £30,000 – £40,000 pa

Hands-on role building, modifying and testing electronic circuits and prototypes, including precision soldering and PCB rework with small surface mount components. Supports engineers with product development and testing, reviews PCB designs in electronics CAD software, and maintains lab equipment while working alongside electronics, mechanical and software engineers.

Omega Resource Group · Gloucester · £45,000 – £50,000 pa

Support and maintain the effectiveness of a medical device manufacturer's QMS in line with ISO 13485, MDR and FDA requirements. Day-to-day work covers CAPA effectiveness, quality data and trend analysis, non-conformances, change control and complaint investigation, plus writing and updating procedures and work instructions.