201 jobs
Johnson & Johnson MedTech Maidenhead
Oversees local UK clinical trials from start-up through database lock, acting as the country-level point of contact and coordinating the local trial team to deliver compliant, high-quality data. Leads feasibility, site selection, recruitment planning and IRAS submissions, while mentoring CTAs and Site Managers and monitoring trial progress against timelines and budget.
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.
Smith & Nephew Cambridge
Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, acting as clinical and commercial expert. You'll support complex surgical cases in theatre, build surgeon relationships, lead product introductions and tenders, and drive adoption of advanced technologies including robotics.
Smith & Nephew Watford
Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, partnering with surgeons and theatre teams on complex cases. Supports procedures in theatre, leads product introductions and tenders, and drives adoption of an innovative portfolio including robotics, working alongside Account and Area Business Managers.
Medtronic Manchester £55,040 – £82,560 pa
Field-based role selling the Hugo robotic-assisted surgery system to existing hospital clients, building coalitions among surgical teams and C-suite budget holders. Involves complex, long capital-equipment sales cycles, business cases, TCO and cost-per-procedure analyses, with 70%+ travel across EMEA.
TRS Consulting Oxford £45,000 – £50,000 pa
Servicing and repairing advanced medical systems and healthcare equipment across the Oxford area, covering electronic, electrical and mechanical faults. Joining a global engineering team focused on long-term customer relationships, with manufacturer product training and a route into more technical specialist roles.
Oxford Nanopore Technologies Oxford
Runs sequencing experiments across the full range of Oxford Nanopore platforms to assess new developments and set performance expectations. Sits within the Product Validation team, working hands-on with sequencing technology to characterise platform capabilities.
Russell Taylor Group Swadlincote £30,000 – £34,000 pa
Supports site validation activities across cleaning, computerised systems, equipment/utilities qualification and process validation, authoring protocols and reports and interpreting data against acceptance criteria. Works cross-functionally to maintain validated status of systems and processes, investigates non-conformances and supports regulatory inspections and internal audits.
HCRG Care Group Runcorn £30,000 pa
Supports and maintains clinical systems, acting as subject matter expert for TPP SystmOne, handling complex incidents, configuration queries, record management and workflow issues. Also trained to become the organisational expert for Hybrid Mail, providing second-line support. Based at a local office with remote support and occasional travel.
SRG Lancashire
Maintains and improves a medical device Quality Management System in line with ISO 13485 and FDA QSR, leading non-conformance, deviation, complaint and CAPA investigations with root cause analysis. Supports internal, supplier and regulatory audits, risk management under ISO 14971, validation and design transfer, working with Manufacturing, R&D, Regulatory Affairs and Supply Chain.
SPD Development Company Ltd Bedford
Provides statistical expertise across R&D, Clinical, Product Support and Marketing, designing and analysing studies and supporting product algorithms and evidence generation. Sits in a three-person Statistical & Data Services Team, acting as statistical representative on assigned projects and communicating findings to technical and non-technical audiences.
Stryker Belfast £12 – £21 ph
Performs visual, dimensional and electrical inspection of sub-assemblies and final medical device assemblies, interpreting prints, drawings and wire lists to approve or reject in-process and final product. Also handles document review and archiving of DHRs, non-conformance quarantine documentation, ERP release transactions and First Article Inspection verification. Night shift role within a GMP-regulated quality team supporting KPI and throughput goals.
Pertemps Gloucester Cheltenham £25,000 – £27,000 pa
Assembling precision medical devices in a controlled cleanroom, following GMP standards, ISO procedures and strict quality requirements to meet production targets. Working a four-day week within a sociable team, with full training provided for candidates from production or manufacturing backgrounds.
Response Personnel Bedfordshire £31,000 – £32,000 pa
Coordinate product development projects from sourcing and concept evaluation through to launch, sourcing materials and prototypes for testing. Maintain product and raw material specifications, work with suppliers on technical and quality requirements, and support cost-effective manufacturing. Provide technical product information to sales and marketing teams while ensuring quality, health and safety and regulatory compliance.
Oxford Nanopore Technologies Oxford
Join the Sequencing Development Team as a Development Scientist, contributing to the development and improvement of sequencing technologies. The role suits a highly motivated individual working within a dedicated scientific team in Oxford.
