Medical Technology Jobs

Johnson & Johnson MedTech · Raritan, United States · US$102,000 – US$177,100 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors performing anonymisation and synthetisation, serves as the primary contact for YODA Project requests, and supports external research teams using clinical study data. Operates independently as a subject matter expert within the Clinical Data Standards and Transparency team.

Johnson & Johnson MedTech · High Wycombe

Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection/submission readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving quality risk monitoring reviews, supporting CAPA plans, and leading inspection readiness and mock inspections with cross-functional teams.

Smith & Nephew · Watford

Lead Business Analyst shaping how Finance and Global Business Services evolve through technology, acting as a trusted advisor to senior leaders. Work spans strategic roadmap development, business analysis, requirements definition and hands-on delivery engagement, managing the ERP enhancement pipeline with a focus on SAP ECC and S/4HANA FICO.

Smith & Nephew · Wrocław, Poland

Acts as a trusted advisor to Finance and Global Business Services teams, translating strategy into technology-enabled change and building business cases through governance. Manages the ERP enhancement pipeline and stays close to delivery, ensuring solutions meet business needs. Requires deep SAP ECC and S/4HANA FICO functional knowledge across complex change programmes.

Medtronic · Warsaw, Poland · PLN 88,000 – PLN 132,000 pa

Primary point of contact for customers through the service and repair journey, managing requests, quotations, orders and escalations while coordinating with service engineers, repair centres and logistics teams. Supports quality and compliance in a regulated MedTech setting and contributes to process improvements, system enhancements and UAT activities.

Medtronic · Madrid, Spain · €27,200 – €40,800 pa

Acts as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations. Collaborates with service engineers, repair centres and logistics teams in a regulated MedTech environment, and contributes to process improvements and UAT activities.

Technical Placements · Gloucester · £65,000 pa

Hands-on international sales role focused on recruiting, onboarding and developing distributor and agent partners across Europe and Latin America for a specialist healthcare manufacturer. Reporting to the General Manager, you will research new markets, negotiate agency agreements, set sales targets and manage partner performance through CRM, with regular international travel.

Clearline Recruitment Ltd · Welwyn Garden City · £38 – £56 ph

Independently manages end-to-end clinical data management across one or more studies, from CRF and database design through to final study closure. Works closely with Biostatistics, Data Science and Clinical Operations, overseeing data vendors and resolving complex issues across EDC, ePRO and IRT systems. Requires strong knowledge of CDISC standards and risk-based monitoring.

Reed Technology · Cambridge · £85,000 – £100,000 pa

Lead information security, product cybersecurity and cyber risk management for a digital health organisation, owning the ISMS, policies and controls. Day to day involves risk assessments, threat modelling, penetration testing oversight, cloud and application security, incident response and supporting audits and regulatory submissions. Works closely with software development, quality, regulatory and clinical teams, acting as the security subject matter expert.

Evolve Selection · Hemel Hempstead

Leads the UK Medical Affairs strategy for an aesthetics organisation, developing integrated brand medical plans and feeding medical insight into a three-year business strategy. Drives evidence generation, publication planning, real-world evidence and KOL engagement while building scientific capability across Commercial and Marketing. Manages a multidisciplinary Medical Affairs team and reports to the Country Manager.

Clearline Recruitment Ltd · Welwyn Garden City · £339 – £500 pd

Coordinate UK clinical study start-up activities and site activation, managing regulatory submissions, approvals and amendments. Liaise with NHS R&D departments, clinical sites and CROs, prepare site contracts, budgets and costing templates, and track timelines and regulatory milestones. Requires hands-on UK start-up experience with HRA, Ethics, MHRA, IRAS, CPMS and ICH-GCP knowledge.

SoCode · Cambridge · £48,000 pa

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.

Platform Recruitment · Royston · £45,000 – £50,000 pa

Develops high-quality, well-documented embedded software in C/C++ on RTOS or bare metal, working across the full lifecycle from requirements capture to verification and release. Sits in multi-disciplinary teams with client-facing communication and significant ownership of design decisions on medical devices.

Computer Futures · London · £75,000 – £85,000 pa

Drive software safety activities across the product lifecycle for software-based medical devices, including hazard analysis, risk assessments and safety documentation. Work with Software, Quality, Regulatory and Product Development teams to ensure compliance with standards such as ISO 14971 and IEC 62304, and support verification, validation and software risk management.

Talentmark · Wrexham · £22 – £29 ph

Translate business requirements into user stories and acceptance criteria, working with a scrum master on story sizing and risk analysis. Participate in release and sprint planning, backlog grooming and sprint reviews, collaborating with software engineers, QA and dev-ops. Focused on clinical trial software such as EDC or eCOA within a 21 CFR Part 11 regulated environment.