83 jobs
Bluetree Cambridge £65,000 – £80,000 pa
Lead regulatory strategy for a cardiology device company expanding into the US, UK, EU and Middle East, owning FDA, CE and UKCA submissions from Class I to Class II/III. Drive an audit-ready QMS (ISO 13485, 21 CFR Part 820, ISO 14971) and advise senior leadership on regulation, quality and clinical governance, working directly with the FDA, MHRA and notified bodies.
NanoFCM CO., LTD Stevenage £26,000 – £40,000 pa
Field-based role installing, maintaining and servicing nano-flow cytometry instruments at customer sites across the UK and Europe, plus remote phone and email troubleshooting of hardware, software and reagents. Involves preventative maintenance scheduling, service documentation, spare parts inventory and coordinating service contracts with the sales team, following training with senior technical staff.
Johnson & Johnson MedTech Titusville, 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, and serves as the primary contact for YODA Project requests, supporting external research teams using clinical study data.
Johnson & Johnson MedTech Spring House, 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.
Smith & Nephew UK - Field
Designs and delivers medical education programmes on Advanced Wound Management across the Nordics, UK & Ireland and Canada, working with healthcare professionals, clinical experts and professional societies. Blends in-person and digital learning, manages programme logistics and outcomes, and collaborates with Medical Education, Marketing, Professional Affairs and Commercial teams. Field-based with extensive travel (up to 70%).
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.
Adecco Surrey £200 – £300 pd
Supports a global pharmaceutical organisation's digital health strategy by identifying and evaluating early-stage opportunities that combine digital technology with healthcare products. Day to day involves market research, business case and value proposition development, external partner assessment, and Agile activities such as sprint planning and OKR reviews, working with commercial, medical, technology and brand teams.
GlobalData Plc Birmingham
Acts as the bridge between pharma consulting teams, the wider business and developers on an AI-enabled competitive intelligence platform running on AWS with Python, PostgreSQL and React. Gathers requirements, maps processes, manages the backlog, coordinates UAT and onboarding, and builds business cases with cost/benefit analysis and value tracking.
GlobalData Plc Birmingham
Builds and runs an AI-enabled competitive intelligence platform for the pharmaceutical market, working end to end from PostgreSQL and Python APIs through to React and TypeScript interfaces. Sits in a small Birmingham-based team, developing data-rich workflows for consulting users and gathering their feedback directly.
GE HealthCare Chalfont Saint Giles
Leads global strategic sourcing and procurement for external manufacturing (CMO) services, covering finished goods, sub-assemblies and specialised components. Drives complex supplier negotiations, market and risk analysis, supplier performance management and contract lifecycle compliance, working cross-functionally with R&D, Engineering, Quality, Supply Chain, Finance and Operations. Hybrid role with global travel.
Medtronic London £87,600 – £131,400 pa
Owns the multi-year product vision and platform strategy for an edge-compute and connectivity foundation used in operating rooms, spanning video, data movement, fleet operations and real-time AI workloads. Works with engineering, clinical and commercial partners in a regulated environment, requiring at least two days a week in the London office.
Newton Colmore Cambridge
Provide regulatory support across a product development organisation, working with engineers and scientists to align projects with global requirements. Maintain and improve the QMS, apply ISO 9001, ISO 13485 and FDA 21 CFR 820, monitor regulatory changes, and support external audits.
Clearline Recruitment Ltd Welwyn Garden City £377 – £550 pd
Operational delivery of early-phase clinical trials, coordinating multi-country study activities, timelines and site start-up while managing vendors, CROs and study documentation such as Trial Master Files. Works closely with international study teams and cross-functional groups to ensure ICH-GCP compliance, manage risks and improve study processes.
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.
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.
