Medical Technology Jobs

• Godmanchester
• Contract

Repairs and maintains medical devices, performing preventative maintenance for service-contract customers and precision instrument servicing under a microscope. Manages personal inventory and stock counts while building relationships with hospital staff and internal sales teams. Field-based role requiring a company vehicle for customer visits.

Microscope

• UK - Field
• Contract

Repair and maintain medical devices, performing preventative maintenance for service-contract customers and precision instrument servicing under a microscope. The role involves inventory management, customer and hospital staff relationships, and completing certification across multiple product franchises, with a company vehicle provided for field-based visits.

Smith+Nephew Equipment

• Edinburgh
• On-site
• Director
• Permanent

This role involves leading and developing a global compliance framework, providing expert guidance on anti-bribery, GDPR, export controls, and ethics. You will ensure alignment with global regulatory and quality standards, oversee whistleblowing processes, and drive compliance risk assessments. The position offers the opportunity to shape compliance strategy in a regulated, innovation-led sector.

• Farnborough
• Remote
• £40,460 – £63,580 pa

Field-based role training hospital staff, technicians and operators on Philips monitoring and ECG equipment across London and South-Central. You run application training schedules, support product launches and demos, and feed customer feedback back to the business unit while working with Account and Product Managers.

Philips Healthcare

• Nottingham
• £16 ph

Carries out laboratory analyses of histopathology samples under senior Biomedical Scientist direction, reporting results accurately and maintaining records. Performs quality control, routine equipment maintenance and consumable management, using computerised data systems. Based at one campus but may work across QMC and Nottingham City Hospital.

• Abingdon
• £50,000 – £55,000 pa
• Lead

Leads a team of five production engineers to drive industrialisation, process improvement, and new product introduction within a regulated medical device environment. Focuses on evolving production systems through automation, Lean methodologies, and design-for-manufacture principles while ensuring quality, scalability, and regulatory compliance. Plays a central role in transitioning next-generation products from development into robust, efficient production.

• Hengoed
• On-site
• Contract

Responsible for ensuring the IT Quality Management System, validation documentation, processes and systems meet applicable GxP and regulatory requirements. Supports the continued development and improvement of the Global IT validation strategy and approach within a pharmaceutical environment.

• Royston
• Hybrid
• £45,000 – £50,000 pa
• Mid-level

Develops high-quality, well-documented embedded software in C/C++ on RTOS or bare metal, working across the full lifecycle from requirements capture to verification and release. Sits in multi-disciplinary teams with client-facing communication and significant ownership of design decisions on medical devices.

Git · Embedded Linux · RTOS

• Christchurch, New Zealand
• On-site
• £60,000 – £65,000 pa
• Senior
• Permanent

Lead automation projects from concept and specification through commissioning, validation and production release, acting as site subject matter expert for automated assembly equipment. Work with Operations, Quality, R&D and external machine builders on robotics, machine vision, laser marking, leak testing and serialization, while mentoring junior engineers and driving continuous improvement.

Siemens · Rockwell · Beckhoff +7

• Cambridge

Hands-on regulatory support across multiple engineering projects, working alongside design engineers and scientists to embed compliance into product development. Applies ISO 9001, ISO 13485 and FDA 21 CFR 820 to interpret requirements, manage design controls and track international regulatory changes. Also supports QMS improvement and external audit preparation.

ISO 9001 · ISO 13485 · FDA 21 CFR 820

• Uttoxeter
• On-site
• £31,000 – £34,000 pa

Manufacture high-accuracy calibration gases and reference materials using gravimetric methods, producing oxygen and flammable gas mixtures to strict ISO 6142 and ISO 17034 standards. Duties include preparing cylinders, valve fitting, stock control and site logistics, working within a specialist production team for a global industrial and medical gases leader.

Microsoft Office

• Birmingham
• £35,000 – £45,000 pa

The Material Specialist will work in the Scientific Research Department, focusing on sourcing, testing, and evaluating new raw materials for medical devices. Key responsibilities include engaging with suppliers, ensuring material traceability and quality, and maintaining high standards through rigorous testing and feedback.

• Bristol
• Hybrid · 2 days in office
• £55,000 – £75,000 pa
• Mid-level
• Permanent

Lead regulatory submissions for Software as a Medical Device products, owning documentation, defining UK, EU and US pathways, and coordinating evidence across software, clinical and quality teams. You'll handle FDA 510(k)/De Novo work, manage regulator and Notified Body interactions, and assess product changes for lifecycle compliance in a small, fast-moving medtech business.

FDA · Notified Bodies

• Aldershot
• On-site
• £45,000 – £55,000 pa
• Mid-level
• Permanent

Hands-on mechanical design role taking safety-critical respiratory protective equipment from concept through 3D CAD modelling, prototyping, testing and production. Involves detailed drawings, DFMEA, jig and fixture design, NPI and technical support, working closely with manufacturing, quality, customers, suppliers and external test organisations.

CREO Parametric · Pro-Engineer Wildfire · SolidWorks

• Stockton-on-Tees
• £40,000 – £46,000 pa

Plans, coordinates and documents process validation activities across NPI and manufacturing projects, preparing protocols, reports and technical evidence. Works with Engineering, Quality, Operations and customers on PPAP submissions, FMEAs and process flow diagrams to demonstrate manufacturing readiness in a regulated medical manufacturing environment.