Medical Technology Jobs

• Zug, Switzerland
• Lead · manages people

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

CARTOSOUND

• Warsaw, Poland
• PLN 217,000 – PLN 350,750 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, partnering with local EP leaders, marketing, health economics and market access to drive adoption, protect the installed base and win new accounts. Combines commercial leadership with strategic account development in a complex matrix.

CARTOSOUND

• Oxford
• On-site
• Mid-level
• Permanent

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.

• Oxford
• On-site
• Senior · manages people
• Permanent

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.

Windows

• Edinburgh
• On-site
• £76,800 – £115,200 pa
• Senior

Own the end-to-end data lifecycle for an AI and algorithm R&D team, from clinical study data collection through validation trials. Design and manage scalable infrastructure across clinical trials, sensor platforms and HPC environments, building ETL/ELT pipelines and data tooling in Python and SQL while shaping data architecture standards.

Python · SQL · C++ +3

• Bedford
• Hybrid · 3 days in office
• £50,000 – £60,000 pa
• Senior

Lead mechanical engineering across the full product lifecycle for fertility and pregnancy diagnostics, from concept and prototyping through to manufacture and launch. The role combines hands-on design in SolidWorks, DFM/DFA, FEA and tolerance analysis with process engineering, risk management (FMEA) and design transfer within a multidisciplinary R&D team, including work with suppliers in China.

SolidWorks · 3D CAD · IVDR +2

• 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.

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

Deliver NPI and engineering projects in a regulated medical manufacturing environment, focusing on process validation, PPAP documentation and quality compliance. Support projects from RFQ and feasibility through validation, customer approval and handover to production, working closely with Engineering, Quality, Operations and customers.

• Bridgwater
• On-site
• £55,000 pa
• Mid-level

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.

• Cambridge
• Hybrid · 2 days in office
• £48,000 pa
• Permanent

Own data management across a portfolio of clinical studies, from setup through database lock and final data transfer, acting as the primary client contact for data quality and delivery. Configure and test data transfers, write production code, produce ETL-based reports, and maintain GCP documentation, with scope to improve SOPs and explore AI tools.

Python · SQL · SAS +2

• Greater Manchester
• Hybrid · 2–3 days in office
• £40,000 – £55,000 pa
• Mid-level
• Contract

Owns a diverse product portfolio in the Life Science/Healthcare sector, managing lifecycle activities from launches and range maintenance to discontinuations. Coordinates with supply chain, finance, regulatory and commercial teams on forecasting, availability and approval of product materials, while analysing market trends to inform decisions and reporting performance to senior stakeholders.

• London
• Hybrid · 2 days in office
• £76,800 – £115,200 pa
• Senior

Builds and maintains modern C++ (C++17+) application software for intra-operative surgical devices, working in a multidisciplinary team spanning embedded, cloud and application software. Responsibilities include device monitoring, cloud connectivity, debugging, and developing secure, medical-grade code compliant with regulatory and security processes.

C++17 · gRPC · DDS +5

• Cambridge
• Remote
• Director · manages people

Leads Jazz's central monitoring capability within Global Clinical Development Operations, defining and interpreting portfolio-level key risk indicators and statistical signals to drive risk-proportionate monitoring strategy at site, study and CRA level. Partners with Trial Risk Management, Site Monitoring, Data Management and Biostatistics, owns RBQM technology platforms, and manages a team of central monitoring analysts.

CTMS · EDC Systems · RBQM Systems +2

• London
• Remote
• Director · manages people

Leads Jazz's central monitoring capability within Global Clinical Development Operations, defining and interpreting portfolio-level key risk indicators and statistical signals to drive risk-proportionate changes in site, study and CRA monitoring strategy. Partners with Trial Risk Management, Data Management and Biostatistics, owns RBQM technology platforms, and manages a team of central monitoring analysts while championing AI-enabled risk detection.

CTMS · EDC

• London
• On-site
• Mid-level

Develops and optimises therapeutic delivery formulations, running lab-based in vitro studies and analytical characterisation to assess stability and performance. Works in a multidisciplinary team progressing early-stage technologies toward manufacturing, with external partner collaboration and scale-up considerations.