251 jobs
Johnson & Johnson MedTech Beerse, Belgium
Supports Clinical Risk Management operational excellence by coordinating process optimisation and day-to-day administration of the CRM digital landscape. Acts as operational point of contact for super-user forums, vendor coordination, taxonomy and metadata stewardship, portal support and audit or inspection evidence. Identifies and implements approved improvements while strategic ownership stays with CRM leadership.
Johnson & Johnson MedTech Issy-les-Moulineaux, France
Supports Clinical Risk Management operational excellence by coordinating process optimisation and the day-to-day administration of the CRM digital landscape. Acts as operational point of contact for super-user forums, vendor coordination, digital asset administration, taxonomy and metadata stewardship, portal support and audit or inspection evidence. Identifies and implements approved improvements while strategic ownership stays with CRM leadership.
Smith & Nephew Hull
Front-line quality role supporting a manufacturing value stream, reviewing and releasing product documentation, generating CoAs/CoCs, and performing raw material inspection. Leads containment, investigation and disposition of non-conforming materials, manages NCs and CAPAs, and acts as an SME during audits.
Smith & Nephew Watford
Leads the design and delivery of AI-enabled supply chain planning solutions on Kinaxis Maestro, owning architecture for advanced forecasting, intelligent planning workbooks and autonomous agents. Partners with business and IT stakeholders, runs workshops and mentors colleagues while defining data integration and governance standards.
Medtronic Heerlen, Netherlands €40,000 – €60,000 pa
Serve 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 centers and logistics teams. Support quality and compliance in a regulated MedTech setting and contribute to process improvements, system enhancements and UAT activities.
Medtronic Heerlen, Netherlands €50,000 – €75,000 pa
Acts as a subject matter expert handling complex customer inquiries, escalations, quotations and orders while driving process improvements and system enhancements. Supports projects, UAT and training within a newly built in-house Service & Repair Customer Care organisation, working in English and French with healthcare providers.
Clearline Recruitment Ltd Welwyn Garden City £339 – £500 pd
Coordinate UK clinical study start-up activities and site activation, managing regulatory submissions, approvals and amendments. Liaise with NHS R&D departments, clinical sites and CROs, prepare site contracts, budgets and costing templates, and track timelines and regulatory milestones. Requires hands-on UK start-up experience with HRA, Ethics, MHRA, IRAS, CPMS and ICH-GCP knowledge.
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.
Aspion Reading £45,000 – £50,000 pa
Field-based business development role selling electronic and electromechanical components across the Thames Valley and Surrey, combining key account management with new business development. You will work with design engineers and procurement teams to secure design-in specifications and manage technical sales pipelines from enquiry through to production, supported by product specialists and application engineers.
Kingston Barnes Ltd Pilning £32,000 – £36,000 pa
Assemble and wire high-tech semiconductor production equipment, working from electrical drawings to solder, crimp and loom complex panel configurations. The role sits in a production team building cutting-edge systems and also involves fault finding and implementing corrective action. Double day shifts with an early Friday finish.
Healthium Clinics Henley-on-Thames £35,000 pa
Supports market access, quality systems and governance across healthcare and technology activity, coordinating evidence packs, tenders and regulatory documentation. Maintains the Quality Management System, risk registers and audit actions, and monitors MHRA, CQC, NICE and ICO requirements. Works with clinical, technical and commercial colleagues to keep registrations and controls inspection-ready.
Ernest Gordon Recruitment Andover £40,000 – £45,000 pa
Maintains and develops the Quality Management System in a high-end cleanroom, supported by a team of six. Ensures compliance with ISO 9001, ISO 13485 and AS9100, applying CAPA, 8D and 5 Whys methods, with training provided where needed. Distinct for its medical devices focus within a growing specialist manufacturer serving aerospace, automotive and medical clients.
Ernest Gordon Recruitment Mitcham £40,000 – £45,000 pa
Field-based role servicing biomedical devices across a London patch, with occasional UK travel and 2-3 overnight stays per month. The technician receives manufacturer-funded training to become certified on high-complexity medical lasers, with progression into more senior positions and time off in lieu for excess hours.
GE HealthCare United Kingdom, YY9 9YY
Provides day-to-day medical oversight for one or more clinical trials, ensuring patient safety, data integrity and protocol compliance. Reviews and assesses AEs and SAEs, supports safety signal detection with Pharmacovigilance, and advises investigators on eligibility and dosing. Works cross-functionally with Clinical Operations, Data Management, Biostatistics and Regulatory Affairs, and contributes to CSRs and regulatory submissions.
Theo James Recruitment Stockton-on-Tees £40,000 – £46,000 pa
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.
