Medical Technology Jobs

• Titusville, United States
• Hybrid
• US$112,000 – US$180,550 pa
• Senior

Operational leader supporting the Immunology regulatory portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates Global Regulatory Team meetings, manages health authority meeting planning and worldwide submissions, and leads change management for new processes and system rollouts across the RPM department.

Veeva · Microsoft Project · Planisware

• Cambridge, United States
• Hybrid
• US$112,000 – US$180,550 pa
• Senior

Operational leader supporting the Immunology regulatory portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates Global Regulatory Team meetings, manages health authority meeting planning and worldwide submissions, and leads change management for new processes and system rollouts. Works with tools like Planisware, Veeva and Microsoft Project.

Veeva · Microsoft Project · Planisware

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

Supports software quality across the full product development lifecycle in Medtronic's surgical operating unit, from requirements and design through verification, validation, release and post-market support. Involves risk management (SFMEA, hazard analysis), design reviews, traceability documentation, CAPA and audit readiness, working closely with software, systems, regulatory and quality teams.

ISO 13485 · ISO 14971 · IEC 62304 +3

• 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

• Malvern
• On-site
• £40,000 – £50,000 pa
• Lead · manages people
• Contract

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.

Business Central

• Berlin, Germany
• Remote
• €156,000 – €234,000 pa
• Director · manages people

Leads commercial growth and adoption of connected care and digital health solutions across Western Europe, structuring multi-year enterprise partnerships with hospital systems. Manages a growing team and works with clinical, IT and executive stakeholders on interoperability, monitoring and data integration. Remote with around 70% regional travel.

HL7 · FHIR · APIs +2

• 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

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

Designs and develops electronic circuits and PCB layouts for medical devices, taking full lifecycle ownership from concept through to manufacturing handover. Work covers schematic capture, component selection, prototyping, debugging and verification against IEC 60601, collaborating closely with mechanical, software and systems engineers. Based on-site in Oxford with some remote design work.

Altium Designer

• 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

• Belfast
• £50,000 – £60,000 pa
• Lead · manages people

Lead the Clinical Method Development and Validation team, overseeing bioanalytical method delivery for a New Product Development programme. The role combines hands-on expertise in extraction techniques and HPLC/UPLC/LCMSMS optimisation with managing and mentoring a team in a GLP-compliant environment, including regulatory submissions and audits.

HPLC · UPLC · LCMSMS +1

• London
• £40,000 – £55,000 pa
• Mid-level

Plan and deliver human factors and usability activities across the full project lifecycle, from study design and fieldwork to analysis and reporting. Moderate research sessions and workshops internationally, applying methods such as contextual inquiry, usability validation and use-related risk analysis for medical devices and healthcare clients.