17 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.
Johnson & Johnson MedTech Beerse, Belgium
Senior analyst role accountable for global PLAN business process validation and release adoption across Transcend EMEA-OTC releases, working with the project team and local business partners to ensure successful release cut-over. Drives process scoping, testing strategy (BST, UAT, regression), solution design workshops, and operational readiness including SOPs and user access management. Serves as the business process single point of contact for PLAN stakeholders through hypercare and post-go-live stabilization.
Johnson & Johnson MedTech Madrid, Spain
Senior analyst role accountable for global PLAN business process validation and release adoption across Transcend EMEA-OTC releases, working with the project team and local business partners on release cut-over. Drives process scoping, testing strategy (BST, UAT, regression), solution design workshops, operational readiness, and hypercare for a multi-year SAP S/4HANA supply chain transformation.
University of Surrey Guildford £48,337 – £70,878 pa
Develop an independent, externally funded research programme as a Principal Investigator, applying AI and data science to human, animal and environmental health data within a One Health framework. Collaborate across medicine, veterinary science, computer science and engineering, secure UK and international funding, publish high-quality work, and teach AI and data science at undergraduate and postgraduate level.
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.
OrganOx Oxford
Hands-on senior role designing, securing and automating Azure cloud infrastructure and CI/CD foundations for regulated medical device software and connected device services. Acts as a bridge between Digital and Data teams, supporting Databricks, SAP interfaces and enterprise data flows, with monitoring, observability and cybersecurity responsibilities. Office-based in Oxford with flexibility.
OrganOx Oxford
Leads a team of Windows software engineers building device-hosted applications and services for Class II and III medical devices, covering GUI development, connectivity and cybersecurity mitigations. Owns the full SDLC, regulatory compliance (FDA, ISO 13485, IEC 62304), roadmaps, budgets and hiring, while acting as technical representative to regulators, partners and customers.
TTP Cambridge
Leads complex medical-device and drug-delivery development programmes from concept through to manufacture, shaping technical strategy amid significant uncertainty. Manages multidisciplinary teams, guides clients through regulatory and commercial decisions, and mentors colleagues while building new business. Based at TTP's Melbourn campus near Cambridge.
SRG Darlington £49,045 – £69,045 pa
Provide senior scientific and technical leadership across complex RNA manufacturing programmes, informing technical strategy, technology selection and GMP translation. Oversee experimental studies, resolve complex challenges and work cross-functionally with technical, operations, quality, engineering and supply chain teams to deliver scalable, GMP-compatible processes.
CV Technical Christchurch, New Zealand £60,000 – £65,000 pa
Lead automation projects from concept and specification through commissioning, validation and production release, acting as site subject matter expert for automated assembly equipment. Work with Operations, Quality, R&D and external machine builders on robotics, machine vision, laser marking, leak testing and serialization, while mentoring junior engineers and driving continuous improvement.
Newton Colmore Cambridge
Medical Devices Consultant - Senior Mechanical Engineer - CambridgeDue to the growth of a leading Medical Devices organisation, we are currently seeking a Senior Mechanical Engineer, Project Manager, Medical Devices Inventor, or Mechanical Design Consultant for a newly approved role....
Newton Colmore Cambridge
Principal Mechanical Design Engineer - Medical Devices - CambridgeA growing Medical Devices team, based in Cambridge, is currently seeking an experienced Mechanical Design Engineer to lead the development of cutting-edge Medical Devices in the fields of Health Technology, Biotech, and...
VK Recruitment Belfast £50,000 – £65,000 pa
Oversee complex production workflows in a specialist dental laboratory, providing technical leadership across CAD/CAM, milling, 3D printing, PMMA, zirconia and ceramics. Troubleshoot equipment and software issues, improve efficiency and quality, and coach technicians and departmental leads. Reports to the Associate Director after a structured induction.
HCRG Care Group Runcorn £50,000 pa
Leads end-to-end data migration projects moving sensitive patient records between Electronic Patient Record systems, coordinating internal teams, external organisations and suppliers. Combines technical project management with data quality, information governance and clinical safety, working closely with the Head of Clinical Systems. Predominantly remote with occasional UK travel.
SGS United Kingdom £30,000 – £32,000 pa
Coordinate and support technical documentation reviews for the UK Medical Devices team, managing review processes, monitoring KPI reports and driving resultant actions. Handle complaints, raise purchase orders for client invoicing, and strengthen key client relationships through calls and meetings. Requires practical experience of Medical Device Regulations or auditing regulations and strong documentation control.
