Medical Technology Jobs

• Stockholm, Sweden
• SEK 709,000 – SEK 1,223,600 pa
• Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) across West EMEA, translating regional strategy into country growth plans and account-level execution. Manages a team of six EP ultrasound clinical specialists, working with local EP leaders, marketing, professional education and market access to drive adoption, protect existing accounts and win new users.

CARTOSOUND

• Madrid, Spain
• €56,100 – €97,635 pa
• Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) across West EMEA, translating regional strategy into country growth plans and account-level commercial execution. Manages a team of six EP ultrasound clinical specialists, partnering with local EP leaders, marketing, professional education and market access to drive procedure adoption, protect existing accounts and win new users. Combines commercial leadership with strategic account development, forecasting, pricing discipline and compliance across a complex matrix.

CARTOSOUND

• Eindhoven, Netherlands
• Remote
• €52,800 – €79,200 pa

Regional product expert for Medtronic's ENT Head & Neck surgical portfolio across Western Europe, driving market development, clinical education and commercialisation. Partners with surgeons, distributors and sales teams to deliver training, lead product launches and build positioning and value propositions. Reports to the Marketing Director and works remotely.

• Madrid, Spain
• Remote
• €38,400 – €57,600 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 and working remotely.

• 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

• Cambridge

Hands-on role designing and integrating optical systems into complex medical devices, from early feasibility through to product launch. You'll work in a multidisciplinary team spanning simulation, prototyping, testing and refinement, with a strong emphasis on regulatory compliance and real-world usability, and mentor junior colleagues.

• 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.

Medical Diagnostic Systems · Laboratory Diagnostics Systems · Clinical Chemistry Systems

• 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.

Medical Diagnostic Systems · Laboratory Diagnostics Systems

• Sheffield
• On-site
• Permanent

Receiving and inspecting medical devices against technical drawings, then labelling, packaging and preparing goods for dispatch. Booking couriers, tracking parcels, supporting the stores and warehouse, and logging customer quality complaints for Regulatory Affairs. Combines hands-on goods handling with SAP-based administration in a busy Technical Services team.

SAP

• Swindon
• Remote
• £45,000 – £55,000 pa
• Mid-level

Owns quality and regulatory affairs for a growing orthopaedic device maker, maintaining ISO 13485, CE and EU MDR approvals and running internal and external audits. Leads the CAPA process and supports new product development, including manufacturing process control and additive manufacturing, drafting procedures and work instructions. Fully remote with flexible hours and real ownership from development through market release.

QMS Software

• Gloucester
• On-site
• £45,000 – £50,000 pa
• Mid-level
• Permanent

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.

ISO 13485 · FDA Quality System

• Cambridge
• £500 – £550 pd
• Senior
• Contract

Contract role building Python and Django software for a medical device client, with TypeScript also in the stack. The work sits in a regulated environment, so prior medical device industry experience is essential and regulated-software background is beneficial. Engaged outside IR35 for an initial six-month term.

Django · TypeScript · Python

• Gloucestershire
• On-site
• £40 – £50 ph
• Mid-level
• Contract

Support the launch and ongoing service of complex medical technology products in a regulated environment, designing processes, documentation, training and workflows for deployment, installation, configuration and support. Provide hands-on Tier 3 technical support, manage customer escalations and transfer new service processes into operations, working with international R&D teams and product owners.

Jira · Azure DevOps

• Hertfordshire
• £37,000 – £41,000 pa
• Entry level

Involves the full product development cycle, from initial concepts and 3D CAD design through to prototyping and testing, within a small medical device manufacturer. Works alongside experienced engineers on varied projects, taking real ownership of designs. Suits someone practical and hands-on with SolidWorks skills.

SolidWorks

• London
• Hybrid
• Mid-level · manages people
• Permanent

Own the regulatory strategy for a venture-backed medical device company preparing its FDA 510(k) submission. Lead the 510(k) through review, act as primary FDA contact, coordinate test evidence across engineering and CROs, and build US post-market processes while shaping UK and EU MDR strategy.

GUDID