The Senior Training & Education Specialist designs, develops, and implements learning solutions to support operational processes, workforce capability, and business performance. The role involves conducting needs analyses, developing curricula, managing projects, and facilitating training sessions across multiple functions and countries.
The Director, Signal Detection Scientist leads the implementation of surveillance strategies for proactive detection and evaluation of safety signals from post-marketing data. Responsibilities include developing and using novel tools and methodologies, performing signal validation, and communicating findings to safety management teams.
This role involves driving software safety activities for medical devices, conducting hazard analysis and risk assessments, and ensuring compliance with medical device standards. You will collaborate with cross-functional teams and support verification and validation processes.
The Compliance Engineer will be responsible for creating, reviewing, and maintaining regulatory and technical documentation to ensure products remain compliant and audit-ready. Key responsibilities include authoring technical files, supporting EU MDR and UK regulatory compliance, and assisting with Notified Body and external audit requirements.
This role involves providing clinical expertise and education in complex wound care, supporting healthcare professionals across North Wales and the Midlands in the effective use of advanced wound management therapies. The specialist will deliver hands-on clinical support, build relationships with decision-makers, and ensure optimal patient outcomes through appropriate product use. The position combines field-based sales with a strong clinical focus in a community care setting.
This role involves providing clinical expertise and education in complex wound care across North Wales and the Midlands, supporting healthcare professionals in community settings to adopt advanced wound management therapies. The specialist will deliver hands-on training, build clinical relationships, and ensure appropriate use of products within their territory. It combines field-based sales with genuine patient impact through clinical advocacy and support.
This role involves leading complex clinical technology transformation and data migration initiatives across the clinical trial ecosystem. Responsibilities include managing end-to-end migration programmes, data validation, and ensuring compliance with regulatory requirements. The position requires strong clinical technology expertise and project management skills.
The Regulatory Affairs Manager will lead day-to-day regulatory activities, maintaining and developing technical documentation for existing and future medical devices and IVD products. You will support UKCA and CE marking, contribute to regulatory strategies, and collaborate with scientific, data, and technical teams to ensure compliance throughout product development.
The Information Security Manager will lead information security, product cybersecurity, and cyber risk management in a highly regulated digital health technology environment. Key responsibilities include maintaining the ISMS, conducting risk assessments, overseeing penetration testing, and embedding cybersecurity in the software development lifecycle.
This role involves managing end-to-end clinical data management for one or more studies, ensuring data quality and integrity. Responsibilities include CRF and database design, data entry, query resolution, and working with cross-functional teams to support high-quality data delivery and continuous improvement.
This role involves leading continuous improvement initiatives, implementing Lean Manufacturing tools, and developing efficient production processes for medical equipment assembly. The candidate will work closely with various departments to improve safety, quality, productivity, and cost efficiency.
This role involves designing and building automated test frameworks for embedded and connected hardware platforms used in operating rooms. Responsibilities include collaborating with engineering teams, developing test automation strategies, and ensuring the reliability and performance of device software and firmware. The position focuses on testing device software, firmware integrations, and hardware-software interactions.
This role involves examining pathological samples using various technologies, ensuring accurate results, and supporting a quality-driven, patient-focused service. You will work as part of a team, manage responsibilities in line with NHS principles, and contribute to innovation and professional development.
Drive sales and strategic account growth for Philips' Hospital Patient Monitoring solutions across NHS Trusts, ICBs, and private hospitals in North East England. Collaborate with clinical and sales teams to deliver integrated, data-driven care solutions, with regular travel to hospital sites for customer engagement and demonstrations. Leverage clinical or medtech sales experience to build stakeholder relationships and improve patient outcomes through connected care technology.
Lead large-scale, cross-functional customer-facing projects in radiology informatics, ensuring delivery within scope, budget, and timeline while managing risks, stakeholders, and subcontractors. Drive financial performance and quality compliance across multi-country implementations. Empower diverse teams and represent projects in governance forums to ensure successful outcomes.
