Medical Technology Jobs

• Manchester
• On-site
• £43,200 – £64,800 pa

Field-based role covering the North West, providing clinical and technical support to electrophysiologists, cardiac physiologists and cath lab teams during cardiac ablation procedures using Cryo, PulseSelect and Affera therapies. Involves procedural troubleshooting, product and therapy training, and supporting installations and launches alongside sales and marketing to drive therapy adoption in assigned accounts.

Cryo · PulseSelect · Affera

• Milan, Italy
• €61,600 – €92,400 pa
• Senior

Defines and executes pricing strategy across a product portfolio and customer segments, analysing pricing trends, diagnostics and levers to hit operating unit objectives. Reviews key tenders and deals, monitors compliance, and works with Western Europe, Japan, Australia/New Zealand and global teams to embed pricing as a strategic profit lever.

Excel

• Maidenhead
• Hybrid
• Mid-level

Responsible for executing study-level activities including creating trial-specific documents, vendor oversight and compound training, plus country and regional oversight of local operational delivery. Aligns feasibility strategy, runs risk reviews, resolves trial issues and supports Health Authority inspections, mentoring new Trial Management team members.

Clinical Trial Management Systems (CTMS)

• Blackpool
• Entry level

Two-year graduate development programme comprising four six-month rotations across functions such as process engineering, continuous improvement, production operations, R&D and quality. Graduates own real projects supporting new product and process introductions, testing and continuous improvement, with mentoring and cross-functional networking in a medical devices environment.

Microsoft Office · CAD

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

Assures software quality across the full lifecycle for medical devices up to IEC 62304 safety class C, covering design controls, requirements, verification and validation, and release management. A central duty is software risk management, developing and maintaining SFMEAs, hazard analyses and cybersecurity risk assessments aligned with ISO 14971. Works with R&D, Engineering, Post-Market Operations, Regulatory Affairs and Cybersecurity to support EU MDR and FDA compliance.

IEC 62304 · ISO 14971 · ISO 13485 +5

• Oxford
• On-site
• Lead
• Permanent

Technical lead for electronics design across current and next-generation medical device products, combining hands-on design with mentoring junior engineers. Defines electronic architecture, reviews schematics and PCB layouts, and oversees verification and validation including EMC and safety testing to IEC 60601, IEC 62304 and ISO 14971 standards. Works closely with suppliers, manufacturing partners, and cross-functional quality and regulatory teams on-site in Oxford.

IEC 60601 · IEC 62304 · ISO 14971

• Cambridge
• Lead · manages people
• Permanent

Leads complex medical-device and drug-delivery development programmes from concept through to manufacture, shaping technical strategy amid significant uncertainty. Manages multidisciplinary teams, guides clients through regulatory and commercial decisions, and mentors colleagues while building new business. Based at TTP's Melbourn campus near Cambridge.

• Aberystwyth
• On-site
• £39,000 – £45,000 pa
• Mid-level
• Permanent

Design and develop scientific monitoring instruments across the full product lifecycle, from schematic capture and PCB layout to prototyping, testing and production handover. Work within an R&D team on analogue and digital circuits, ARM microcontrollers, EMC compliance and automated test, supporting ISO 9001/14001 phase-gate processes.

Altium Designer · Oscilloscopes · Logic Analysers +7

• Cambridge
• Remote
• Lead

Lead statistician responsible for the statistical design, analysis and reporting of Phase I–IV clinical trials and regulatory filings, including writing and reviewing statistical analysis plans and validating CRO deliverables. Works cross-functionally with clinical development, regulatory affairs and medical writing, using SAS and R, with CDISC standards and Bayesian/adaptive design experience preferred.

SAS · R

• London
• Remote
• Lead

Lead statistician responsible for the statistical design, analysis and reporting of Phase I–IV clinical trials and regulatory filings, including writing and reviewing statistical analysis plans and validating CRO deliverables. Works cross-functionally with clinical development, regulatory affairs and medical writing, using SAS and R, with CDISC standards and Bayesian or adaptive designs preferred.

SAS · R

• 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

• Burgess Hill
• On-site
• £32,000 – £40,000 pa

Coordinating quality processes, managing non-conformances, supporting investigations and corrective actions, and maintaining ISO 9001 and ISO 13485 compliance. Reporting to the Head of Quality, the role covers document control, CAPA, supplier quality and audit support within a regulated packaging business, with scope to broaden experience across auditing and regulatory compliance.

Microsoft Office

• 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

• Henley-on-Thames
• £32,000 – £38,000 pa
• Mid-level
• Permanent

Support regulatory affairs and compliance across healthcare, digital health and medical-device activity. Maintain the Quality Management System, medical-device technical documentation, risk registers and audit actions, while coordinating evidence for tenders, CQC inspections and information governance. Acts as a link between clinical, technical and commercial teams.

ISO 13485 · ISO 14971 · IEC 62304 +7

• Hatfield
• Lead · manages people

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.

GE HealthCare Patient Care Solutions · GE HealthCare Ultrasound Systems · Servers +2