Medical Technology Jobs

Johnson & Johnson MedTech · Zug, Switzerland

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.

Johnson & Johnson MedTech · Horsham, United States · US$117,000 – US$201,250 pa

Leads the development, revision and maintenance of primary labeling documents including the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrixed regulatory affairs team.

TRS Consulting · Milton Keynes · £45,000 – £55,000 pa

Home-based account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. Involves managing key customer accounts, identifying new business, attending exhibitions and local events, analysing competitor activity and producing proposals and sales agreements to exceed area sales targets.

TRS Consulting · Birmingham · £45,000 – £55,000 pa

Account management role selling multi-vendor service contracts across biomedical, ultrasound and endoscopy product ranges. You manage key customer accounts, identify new business, attend exhibitions and local events, analyse competitor activity and produce proposals and sales agreements to exceed area sales targets.

Medtronic · London · £77,040 – £115,560 pa

Serves as a senior scientific expert for the Neuromodulation & Pelvic Health portfolio, leading external scientific engagement with KOLs, healthcare professionals and medical societies across Western Europe. Delivers evidence-based clinical information, runs advisory boards, CME programmes and congress activities, and partners with clinical, regulatory and commercial teams on medical affairs strategy. Remote UK-based role with frequent travel.

Platform Recruitment · London

Develops and optimises therapeutic delivery formulations, running lab-based in vitro studies and analytical characterisation to assess stability and performance. Works in a multidisciplinary team progressing early-stage technologies toward manufacturing, with external partner collaboration and scale-up considerations.

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.

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.

Matchtech · Fareham

Maintains and improves a medical device Quality Management System, planning and reporting internal audits and leading external audit readiness with evidence packs and follow-up actions. Supports ISO 13485 compliance, ISO 14971 risk activities, CAPA and document control, and leads quality improvement projects in a regulated scale-up environment.

Randstad Construction & Property · London

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships to deliver Patient Cloud projects on time and within budget. Involves risk assessment, study documentation, and meetings, with expertise in eCOA/ePRO, eConsent, virtual trials or wearables. Fully remote, but requires flexibility to work American time.

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.

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.

QIAGEN · Remote United Kingdom

Field-based role owning a strategic territory across the North of the UK and Ireland, driving sales growth for QuantiFERON tuberculosis diagnostics while exploring transplantation market opportunities. Involves building relationships with clinicians, laboratories and KOLs, delivering clinical presentations, and managing activity through Salesforce CRM, with up to 80% travel.

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.