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. Requires 5+ years in clinical trial execution and GCP knowledge.
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.
Defines and executes pricing strategy across a product portfolio and customer segments, analysing pricing trends, diagnostics and levers to hit operating unit objectives. Reviews tenders and deals against revenue and profit expectations, advising country business units and senior management. Works cross-functionally with Western Europe, Japan, Australia/New Zealand and global teams to embed pricing as a strategic profit lever.
Defines and executes pricing strategy across a product and service portfolio, analysing trends, running diagnostics and modelling opportunities in Excel. Partners with country, regional and global teams across Western Europe, Japan and Australia on tenders, deals and value-based healthcare programmes, driving pricing mindset change in a matrix organisation.
Set up and support surgical camera systems, inspecting, troubleshooting and replacing medical devices while providing clinical-area client support. Deliver training to staff at all levels and complete weekly and quarterly reports. Based with a global medical instrument manufacturer, working in healthcare and operating theatre environments.
Set up and support surgical camera systems, inspect and troubleshoot medical devices, and provide clinical-area client support so staff can focus on patient care. Deliver training to all staff levels and complete weekly and quarterly reports. Based with a long-established medical device manufacturer, working in healthcare and operating theatre environments.
Hands-on role designing custom electronic circuit boards from customer requirements, covering schematic capture, PCB layout, board bring-up, verification and test. You'll liaise with clients on integration and commissioning, write technical reports, and work across IoT, medical device and robotics projects in a consultancy team.
Plans, coordinates and documents process validation activities across NPI and manufacturing projects, preparing protocols, reports and technical evidence. Works with Engineering, Quality, Operations and customers on PPAP submissions, FMEAs and process flow diagrams to demonstrate manufacturing readiness in a regulated medical manufacturing environment.
Deliver NPI and engineering projects in a regulated medical manufacturing environment, focusing on process validation, PPAP documentation and quality compliance. Support projects from RFQ and feasibility through validation, customer approval and handover to production, working closely with Engineering, Quality, Operations and customers.
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.
Design and develop complex injection moulded plastic components and polymer-based medical devices, focusing on scalability, manufacturability, and regulatory compliance. Lead concept-to-production design projects involving robotics and mechatronics, working closely with manufacturing partners and cross-functional teams. Engage in hands-on prototyping, materials selection, and design validation within a regulated medtech environment.
Assemble medical devices to engineering drawings and design specifications, checking components and sub-assemblies against relevant standards. Work methodically to tight deadlines within a production team, completing documentation and performing quality assurance activity to independently release product under final approval processes.
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.
Hands-on R&D role designing and improving electro-mechanical medical devices for women's health and fertility, covering schematic capture, PCB layout in Altium, verification and validation testing, EMC and IEC 60601 electrical safety compliance, and hardware/software integration. Works within a collaborative international R&D team on both new product development and sustaining engineering, with prototyping, debugging and technical documentation duties.
Lead and contribute to technically ambitious surgical device projects, applying ultrasound expertise across the innovation lifecycle from early feasibility to product launch. Engage directly with clients to shape strategy and grow a presence in the surgical technology community, working on robotic-assisted surgery systems and intelligent instruments with embedded sensors.
