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 · 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.

Smith & Nephew · Hull

Leads strategic initiatives to shape and continuously improve a global compliance programme, simplifying processes, enhancing systems and overseeing reporting, communications and training roadmaps. Works cross-functionally with Compliance, Finance and People teams, measuring programme effectiveness and supporting leadership reporting.

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.

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.

Medtronic · London · £95,200 – £142,800 pa

Builds and maintains the internal platform tooling that other engineering teams rely on, spanning Infrastructure as Code with OpenTofu, EKS and Helm, CI/CD automation, and observability with OpenTelemetry. Also supports AI agentic workflows and designs pragmatic fixes for developer productivity gaps, mentoring engineers across the organisation.

Platform Recruitment · Cambridge · £35,000 – £45,000 pa

Develops FPGA and embedded firmware for high-performance data acquisition and signal processing systems used in biomedical research products. Writes VHDL for FPGA functionality and C for low-level hardware control, integrating and debugging digital electronics across the full product lifecycle alongside hardware and software engineers.

QIAGEN · Manchester

Lead the global Medical Affairs strategy for an oncology precision diagnostics portfolio, shaping biomarker and companion diagnostic initiatives with pharma and biotech partners across the drug development lifecycle. Engage key opinion leaders and cross-functional teams in a matrixed international environment, representing the company at conferences and advisory boards.

Sue Ross Recruitment Ltd · Sheffield · £32,000 pa

This role involves driving sales of medical devices through a consultative, virtual-first approach, combining clinical and technical expertise with strong account management. The candidate will identify customer needs, deliver product solutions, and develop strategic business plans to grow both existing and new accounts. Success requires analytical insight, proactive market awareness, and effective communication across video, phone, and in-person channels.

SoCode · Cambridge · £400 – £500 pd

Hands-on contract role running usability studies for advanced medical devices, covering the full study cycle from planning and moderating or observing sessions to analysing data and writing regulation-ready reports. The first project is a formative field study on cleaning and reprocessing workflows with real users, working alongside an established in-house human factors team following FDA-aligned quality procedures.

HAYS Specialist Recruitment · Oxford

Provide quality oversight across clinical activities and the Quality Management System, leading internal, external and vendor audits, managing quality events, CAPAs and root cause investigations, and supporting regulatory inspection readiness. Work cross-functionally with Clinical Operations, Pharmacovigilance, Regulatory Affairs and Quality to drive compliance across GCP, GCLP and GVP activities.

Talentmark · Welwyn Garden City · £38 – £60 ph

Independently manage end-to-end clinical data management for one or more studies, from CRF and database design through to final study closure. Collaborate with Biostats, Data Science and Clinical teams to define data specifications, resolve complex data issues using risk-based monitoring, and oversee third-party vendors to meet regulatory and quality expectations.