31 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.
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.
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.
Real Tipperary, Ireland £52 – £60 ph
Supports the development and improvement of complex medical devices within a multidisciplinary engineering team, covering the full product lifecycle from concept and mechanical design through prototyping, testing, verification, validation and commercial launch. Also involves failure investigation, sustaining engineering, design improvements and compliant design and risk-management documentation.
Johnson & Johnson MedTech Blackpool
Accountable technology leader for the DePuy Synthes EMEA Deliver domain, owning the regional logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances multi-year transformation delivery with operational reliability, cybersecurity, compliance and lifecycle governance, while leading a team and governing 3PL and vendor technology relationships.
Johnson & Johnson MedTech Blackpool
Performs physical, analytical and chemical QC testing on raw materials, in-process and finished products, and leads laboratory and non-conformance investigations. The role covers GMP documentation, equipment calibration, method validation and consumable management while ensuring compliance with ISO 13485, ISO 14001 and FDA QMSRs. It also involves training other staff and liaising with approved manufacturers to keep testing on schedule.
Medtronic London £76,800 – £115,200 pa
Supports software quality across the full product development lifecycle in Medtronic's surgical operating unit, from requirements and design through verification, validation, release and post-market support. Involves risk management (SFMEA, hazard analysis), design reviews, traceability documentation, CAPA and audit readiness, working closely with software, systems, regulatory and quality teams.
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.
Newton Colmore Cambridge
Lead multiple electro-mechanical medical device projects, taking on mechanical design work directly while mentoring junior staff. Requires hands-on development experience with EN60601 and ISO 13485 standards, plus regular communication with internal and external stakeholders.
Newton Colmore Cambridge
Lead multiple programmes advancing next-generation drug delivery platforms, mentoring junior engineers while owning core mechanical design work. Requires hands-on experience with autoinjectors, inhalers, infusion systems or wearable devices, translating clinical and regulatory requirements into robust mechanical solutions. Involves close collaboration with internal teams, external partners, clients and suppliers, with electro-mechanical device experience advantageous.
Ripple Luton £65,000 pa
Hands-on operational leadership across manufacturing, quality assurance, supply chain, purchasing and facilities at a medical equipment manufacturer. Sits on the Senior Leadership Team, owning site health and safety, ISO compliance and continuous improvement, while partnering with executive leadership on business planning and representing the site at group forums.
SoCode Cambridge £80,000 – £100,000 pa
Job Title: Senior QA Validation EngineerLocation - Cambridge: On Site (some flex on occasionSalary - £80k - £100k (depending on experience) + up to 10% bonus (company performance dependent) + equityOverviewWe are seeking an experienced Senior QA Validation Engineer to...
GE HealthCare United Kingdom, YY9 9YY
Owns GE HealthCare's strategic relationships with NHS Trusts and private clinics across the North East, driving the full sales cycle for medical imaging capital equipment including CT, MR, MI, X-ray and Women's Health. Works within a matrixed organisation alongside a team of Imaging Account Managers, managing CRM forecasting, tender processes and long-term account strategy.
Reed Stroud £58,000 – £63,000 pa
Lead packaging and labelling validation for medical devices, managing transportation testing, shelf-life studies and equipment validation projects. Review technical documentation, BOMs and labelling content, drive process improvements, and lead non-conformance and CAPA investigations. Act as key contact during internal, customer and regulatory audits, supporting regulatory submissions and mentoring junior team members.
Reed Stroud £58,000 – £63,000 pa
Lead packaging and labelling validation for medical devices, managing transportation testing, shelf-life studies and equipment validation projects. Review technical documentation, BOMs and labelling content, drive process improvements, and lead non-conformance and CAPA investigations. Act as key contact during internal, customer and regulatory audits, supporting regulatory submissions and mentoring junior team members.
Appcast Enterprise Clonmel, Ireland
Supports manufacturing operations by optimising processes, monitoring equipment and resolving issues that cause non-conforming products or low yields. Works within a quality system environment, interfacing with quality and R&D teams to integrate new products and processes, and participates in validation activities. May lead project teams and mentor less experienced engineers.
