69 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 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.
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.
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.
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.
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.
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.
