47 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.
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.
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.
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.
Matchtech Fareham
Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.
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 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.
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%).
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.
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.
