Medical Technology Jobs in Exeter

Wallace Hind Selection · Montpellier, France · £45,000 – £48,000 pa

Field-based role owning an established South West England and Wales territory for an international medical equipment manufacturer, selling into NHS and private hospitals across departments such as A&E, Renal, Oncology and Day Surgery. Involves rebuilding a neglected region, developing existing accounts and new business through complex multi-stakeholder procurement processes, with regular travel and trips to France for training and meetings.

Wallace Hind Selection · Swindon · £45,000 – £48,000 pa

Field-based role owning an established South West England and Wales territory for a medical equipment manufacturer, selling into NHS and private hospitals across departments such as A&E, Renal, Oncology and Day Surgery. Involves rebuilding a neglected region through new-business development, product demonstrations and navigating complex multi-stakeholder procurement processes, with autonomy to manage your own pipeline.

Medtronic · Southampton · £41,200 – £61,800 pa

You will integrate the HUGO robotic-assisted surgery system into hospitals, developing program goals, surgeon and staff training plans, and supporting cases during learning curves. The role involves change management with clinical stakeholders and close work with field service engineers, requiring over 75% travel across the UK and Ireland.

Medtronic · Manchester · £41,200 – £61,800 pa

You will lead the integration of the HUGO RAS system into hospitals, developing program goals, surgeon and staff training plans, and driving technology adoption through change management. The role involves coaching clinical teams to self-sufficiency and coordinating with field service engineers, requiring over 75% travel across the UK and Ireland.

CV Technical · Christchurch, New Zealand · £60,000 – £65,000 pa

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.

TRS Consulting · Bristol · £42,000 pa

Servicing and repairing sophisticated medical and laboratory diagnostics systems in pathology departments, NHS labs and clinical chemistry sites. The role involves travelling to customer sites, troubleshooting high-value capital equipment and liaising with laboratory managers and technicians. Full product training is provided, so candidates from other field service backgrounds are considered.

TRS Consulting · Weston-super-Mare · £42,000 pa

Servicing and repairing sophisticated medical and laboratory diagnostic systems in pathology departments, NHS labs and clinical chemistry settings. The role involves visiting customer sites, troubleshooting high-value capital equipment and liaising with laboratory managers and technicians. Full product training is provided, so candidates from other field service backgrounds are considered.

GE HealthCare · Hatfield

Lead a team of technicians in a repair centre, coordinating daily workloads while hands-on repairing and troubleshooting Patient Care Solutions and Ultrasound systems down to component level. Prepare quotations, manage parts and inventory, install and test hardware and software, and ensure ISO 9001 compliance and customer communication.

Nomad Mediation · United Kingdom · £40,000 – £45,000 pa

Reporting to the Quality Manager, you will maintain and improve a supplier approval system across ISO 9001, ISO 13485, BS EN 14065, ISO 14001 and ISO 50001. The role involves planning and performing external supplier audits, including international travel, closing out corrective actions, and partnering with Procurement on supplier selection and risk. You will also run internal audits and monitor Supplier Quality KPIs and CAPAs.

Hudson Shribman · United Kingdom · £55,000 – £70,000 pa

This role involves leading and executing in-vitro toxicology studies, including Neutral Red, Ames, and micronucleus assays, within a regulated laboratory environment. The scientist will develop and optimise testing methodologies, interpret complex biological data, and support regulatory submissions. They will work collaboratively across multidisciplinary teams and with external partners to advance pre-clinical testing capabilities in product safety assessment.

Real · Tipperary, Ireland · £52 – £60 ph

Supports the development and improvement of complex medical devices within a multidisciplinary engineering team, covering the full product lifecycle from concept and mechanical design through prototyping, testing, verification, validation and commercial launch. Also involves failure investigation, sustaining engineering, design improvements and compliant design and risk-management documentation.

Matchtech · Fareham

Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.

Azenta Life Sciences · Dorking

Azenta is seeking a highly motivated and experienced Quality Engineer to join our dynamic team in Wotton, Surrey. This is a permanent, onsite role suited to someone who thrives in a fast-paced manufacturing environment and brings strong problem solving capabilities,...

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.

Hyper Recruitment Solutions · Hertfordshire

Own product regulatory compliance end to end, acting as the company's official representative and evidencing compliance to external parties. Advise on sourcing, development, composition, packaging, labelling and marketing, horizon-scan regulatory changes, and support domestic and European product registrations plus safety data sheet software. Requires REACH/CLP knowledge and a chemical or QA background.