50 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 Beerse, Belgium €79,800 – €137,770 pa
Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, securing clinical team approvals. Supports external research teams using clinical study data.
Smith & Nephew Hull
Leads a large packaging operations team including Line Leaders, Operators and Process Technicians, owning People, Safety, Quality, Cost and Delivery. Drives value-stream mapping, Kaizen projects and operational excellence, with accountability for Tier 2 actions and the operation's P&L, OEE, MUV and labour efficiency. Requires a manufacturing supervision background and shift flexibility.
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%).
Johnson & Johnson MedTech Espoo, Finland
Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists healthcare professionals with post-operative outcome analysis and new product introductions. Home-office based with up to 20% travel, reporting to the Associate Director of Clinical Services.
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.
Industrious Recruitment Milton Keynes £37,500 pa
Provide first-line remote technical support for specialist laboratory analysers and medical devices, diagnosing faults using remote-access tools such as RDP, VNC and augmented reality. Work with laboratory staff, field service engineers and product specialists to resolve issues and minimise on-site visits, while training users and maintaining service records.
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.
Real Glasgow £60 – £75 ph
Design, develop and test electronic systems and components, covering circuit design, schematic capture, PCB layout, troubleshooting, design reviews and project documentation. Works with cross-functional teams on robust, compliant solutions, with analogue, power supply, EMC and Altium skills; medical devices experience is desirable.
SoCode Cambridge £50 – £65 ph
Embedded contractor role within an established medical technology company's electronics team, supporting complex designs from requirements and schematic capture through design reviews, PCBA layout, board bring-up and system test. Requires broad electronics design experience with depth in areas such as embedded microprocessors, motor drives, FPGA, analogue sensors or high-speed communications, using Altium Designer and DFx/EMC principles.
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.
GE HealthCare United Kingdom, YY9 9YY
You will install, maintain and repair CT, PET and Nuclear Medicine systems across the Midlands and wider UK, diagnosing complex multi-technology faults and providing remote diagnostics from a home office. The role involves roughly 35-40% travel with occasional overnight stays, plus overtime, short-notice callouts and weekend shifts, working closely with healthcare professionals and engineering teams.
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.
