Medical Technology Jobs

Ernest Gordon Recruitment · Andover · £40,000 – £45,000 pa

Maintains and develops the quality management system in a high-end cleanroom, ensuring compliance with ISO 9001, ISO 13485 and AS9100, with training provided where needed. Uses CAPA, 8D and 5 Whys to drive quality standards, supported by a team of six. Works Monday to Thursday 8:30am-5pm with an early Friday finish.

Russell Taylor Group · Deeside · £29,000 – £34,000 pa

Supports diagnostic testing, assay development and IVD kit manufacture within an established scientific team. Day-to-day work includes processing client samples, operating PCR and capillary sequencing equipment, running quality control checks and managing stability storage. Also involves data analysis, report writing and taking ownership of assigned projects.

Oxford Nanopore Technologies · Oxford

Join the Biologics Tech Transfer team to support the onboarding and scale-up of production for analyte and other components used in sequencing kits. The role centres on transferring and scaling biological production processes within a biotech manufacturing environment.

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.

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.

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.

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.