186 jobs
Johnson & Johnson MedTech Breda, Netherlands €64,000 – €103,040 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, system integrations, release management, UAT, end-user support and training, plus automation, analytics and GenAI improvements. Hybrid role with up to 10% travel.
Johnson & Johnson MedTech Leiden, Netherlands €64,000 – €103,040 pa
Supports Clinical Trial Management Solutions (CTMS, Site Payments, Access Provisioning) as a liaison between business teams, IT and suppliers. Handles study build, release management, UAT, integrations, end-user support and audits, and drives automation, analytics and GenAI improvements. Hybrid working with up to 10% international travel.
Medtronic Milan, Italy €31,200 – €46,800 pa
Acts as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations while coordinating with service engineers, repair centres and logistics teams. Supports quality and compliance in a regulated MedTech setting and contributes to process improvements, system enhancements and UAT activities.
Medtronic London £76,800 – £115,200 pa
Designs, benchmarks and optimises deep learning models for computer vision and surgical video understanding, focusing on low-latency inference on edge and cloud devices. Works with ML, platform and embedded engineers on end-to-end video pipelines, temporal reasoning and model optimisation techniques such as pruning, quantisation and TensorRT.
Wallace Hind Selection Slough £35,000 – £40,000 pa
Consultative field sales role promoting vascular access and oncology medical devices to NHS and private healthcare customers across the M25 region. Roughly 80% new business generation and 20% account development, including quotations, equipment demonstrations, and attendance at fairs and congresses, with full training and mentoring provided.
Talentmark Stirling £25 – £27 ph
Execute complex experimental workstreams from concept through to design transfer, analysing multi-factorial data and presenting technical findings to stakeholders. Apply Design for Manufacture principles to optimise product formulations and characterisation, while upholding GLP, GMP and GDP compliance in a fully site-based laboratory. Requires diagnostic immunoassay expertise, ideally with particle-based assays and fluorescent detection.
Talentmark Welwyn Garden City £38 – £60 ph
Independently manage end-to-end clinical data management for one or more studies, from CRF and database design through to final study closure. Collaborate with Biostats, Data Science and Clinical teams to define data specifications, resolve complex data issues using risk-based monitoring, and oversee third-party vendors to meet regulatory and quality expectations.
Newton Colmore Cambridge
Senior Mechanical Engineer - Biotech Mechatronics - CambridgeA spin-out Biotech company, based in Cambridge, is currently hiring several Senior Mechanical Engineers to join them and help accelerate the proof of concept, design, development, building, and testing of a novel life-saving...
QIAGEN Manchester
Designs analytical, clinical and performance studies to demonstrate the safety and effectiveness of diagnostic products, developing statistical analysis plans and programming analyses in SAS or R. Works within a globally connected Statistics and Data Science team alongside Product Development colleagues in Manchester, Germany, Spain and the USA, presenting results and contributing to regulatory documentation. Seniority determines whether the postholder mentors colleagues and drives process improvement.
Avanti Recruitment ELY £65,000 – £75,000 pa
Hands-on R&D role developing advanced sensing and measurement technology, owning electronics from concept and architecture through PCB design, prototype bring-up, testing and production. Focus on low-noise analogue and mixed-signal electronics alongside high-speed digital, FPGA and microcontroller hardware, with signal integrity work on complex multi-layer boards.
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.
ProTech Recruitment Ltd Hertfordshire £37,000 – £41,000 pa
Involves the full product development cycle, from initial concepts and 3D CAD design through to prototyping and testing, within a small medical device manufacturer. Works alongside experienced engineers on varied projects, taking real ownership of designs. Suits someone practical and hands-on with SolidWorks skills.
Spire Healthcare Elland
Operational lead for the hospital's medical device management programme, acting as subject matter expert for equipment lifecycle, maintenance, asset control and regulatory compliance. Day to day involves managing biomedical equipment work orders, liaising with clinical departments and third-party engineers, training staff and running asset tagging and quarantine checks.
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.
