Medical Technology Jobs

Smith & Nephew · Derby

Field-based clinical sales role covering North Wales and the Midlands, acting as the go-to expert for complex wound care within the Advanced Wound Management portfolio. Involves hands-on clinical support, education and relationship building with community healthcare professionals, guiding decision makers and strengthening advocacy for therapies across the territory.

Smith & Nephew · UK - Field

Designs and delivers medical education programmes on Advanced Wound Management across the Nordics, UK & Ireland and Canada, working with healthcare professionals, clinical experts and professional societies. Blends in-person and digital learning, manages programme logistics and outcomes, and collaborates with Medical Education, Marketing, Professional Affairs and Commercial teams. Field-based with extensive travel (up to 70%).

Progress Sales Recruitment · Birmingham · £55,000 – £65,000 pa

Owns a field-based territory selling wound care products and solutions into the NHS, from strategic account planning and prospecting through to negotiation, implementation and account growth. Involves building relationships with senior clinical, procurement and ICB stakeholders and supporting formulary and pathway adoption discussions.

Johnson & Johnson MedTech · Raritan, United States · US$137,000 – US$235,750 pa

Leads the Accelerando program management function, partnering with high-priority new product development teams to de-risk and accelerate clinical trial execution. Acts as a trusted advisor to Compound Development Teams, running critical path analysis, threat and opportunity assessments, and project planning in Planisware and MS Project. Also leads a team, drives best-practice adoption and benchmarking across a global matrix organisation.

Johnson & Johnson MedTech · Spring House, United States · US$137,000 – US$235,750 pa

Leads the Accelerando program management function, acting as a trusted advisor to Compound Development Teams to de-risk and accelerate priority drug development programs. Facilitates cross-functional project planning in Planisware, conducts critical path and threat/opportunity analyses, and drives best practices and process improvements across a global matrix organisation.

L-ev8 Recruitment Ltd · Burgess Hill · £32,000 – £40,000 pa

Coordinating quality processes, managing non-conformances, supporting investigations and corrective actions, and maintaining ISO 9001 and ISO 13485 compliance. Reporting to the Head of Quality, the role covers document control, CAPA, supplier quality and audit support within a regulated packaging business, with scope to broaden experience across auditing and regulatory compliance.

Clearline Recruitment Ltd · Welwyn Garden City · £38 – £56 ph

Independently manages end-to-end clinical data management across one or more studies, from CRF and database design through to final study closure. Works closely with Biostatistics, Data Science and Clinical Operations, overseeing data vendors and resolving complex issues across EDC, ePRO and IRT systems. Requires strong knowledge of CDISC standards and risk-based monitoring.

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.

SoCode · Cambridge · £48,000 pa

Own data management across a portfolio of clinical studies, from setup through database lock and final data transfer, acting as the primary client contact for data quality and delivery. Configure and test data transfers, write production code, produce ETL-based reports, and maintain GCP documentation, with scope to improve SOPs and explore AI tools.

Aurora Life Sciences · Leeds · £55,000 – £60,000 pa

Hands-on quality engineering role supporting medical device manufacturing across validation, design changes, non-conformance investigations and risk management. The post-holder leads root cause investigations, owns complex quality issues and drives corrective actions, working cross-functionally and mentoring junior engineers. Suits someone who prefers solving manufacturing problems over pure documentation and compliance work.

HAYS Specialist Recruitment · Oxford

Provide quality oversight across clinical activities and the Quality Management System, leading internal, external and vendor audits, managing quality events, CAPAs and root cause investigations, and supporting regulatory inspection readiness. Work cross-functionally with Clinical Operations, Pharmacovigilance, Regulatory Affairs and Quality to drive compliance across GCP, GCLP and GVP activities.

Planet Recruitment · Abingdon · £28,000 – £35,000 pa

Create, maintain and publish technical documentation including Instructions for Use, service manuals, production procedures and product artwork for medical devices. Work with engineering, quality and production teams to verify technical information, manage change control and prepare files for printing. Involves desktop publishing, technical illustrations and coordinating external translations.

Azenta Life Sciences · Dorking

Azenta is seeking a highly motivated and experienced Quality Engineer to join our dynamic team in Wotton, Surrey. This is a permanent, onsite role suited to someone who thrives in a fast-paced manufacturing environment and brings strong problem solving capabilities,...

Vector Recruitment · Larbert

Lead the development of next-generation electrochemical biosensors and diagnostic assays while remaining hands-on in experimental design, data interpretation and sensor development. The role spans electrochemistry, sensor engineering, biofunctionalisation, assay development and manufacturability, working with scientists, engineers and commercial teams to turn concepts into viable diagnostic products. It combines scientific leadership and mentoring with deep technical involvement rather than pure management.

Newton Colmore · Cambridge

Hands-on regulatory support across multiple engineering projects, working alongside design engineers and scientists to embed compliance into product development. Applies ISO 9001, ISO 13485 and FDA 21 CFR 820 to interpret requirements, manage design controls and track international regulatory changes, while supporting QMS improvement and external audit preparation.