Medical Technology Jobs

• Edinburgh
• On-site
• £76,800 – £115,200 pa
• Senior

Own the end-to-end data lifecycle for an AI and algorithm R&D team, from clinical study data collection through validation trials. Design and manage scalable infrastructure across clinical trials, sensor platforms and HPC environments, building ETL/ELT pipelines and data tooling in Python and SQL while shaping data architecture standards.

Python · SQL · C++ +3

• Oxford
• On-site
• Senior
• Permanent

Hands-on senior role designing, securing and automating Azure cloud infrastructure and CI/CD foundations for regulated medical device software and connected device services. Acts as a bridge between Digital and Data teams, supporting Databricks, SAP interfaces and enterprise data flows, with monitoring, observability and cybersecurity responsibilities. Office-based in Oxford with flexibility.

Azure · Databricks · SAP

• London
• Hybrid · 2 days in office
• £76,800 – £115,200 pa
• Senior

Designs, builds and maintains a Python-based SaaS platform for project, data and annotation management used by internal machine learning engineers and data scientists. Works with data and platform engineers to handle growing data volumes, and collaborates with stakeholders to define requirements and validate features in an iterative, quality-driven environment.

AWS · GCP · Docker +2

• London
• Senior

Own the technical delivery of AI initiatives end to end, taking HealthHero's flagship Clinical Brain from prototype to production. The role involves designing an AI layer that interacts with deterministic components of a Class II medical device, combining NLP, LLMs and machine learning, and building rigorous evaluation pipelines with golden datasets, mixtures of evaluators and human-in-the-loop clinician review.

AWS · GCP · Azure +7

• London
• Senior

Owns end-to-end delivery of AI initiatives, starting with the Clinical Brain, a Class II medical device combining an AI layer with deterministic components. Involves NLP, LLMs, knowledge graphs, rigorous evaluation with golden datasets and clinician review, plus LLMOps and regulated documentation alongside clinical and compliance leads.

Neo4j · Cypher · GraphRAG +5

• Blackpool
• Entry level

Two-year graduate development programme comprising four six-month rotations across functions such as process engineering, continuous improvement, production operations, R&D and quality. Graduates own real projects supporting new product and process introductions, testing and continuous improvement, with mentoring and cross-functional networking in a medical devices environment.

Microsoft Office · CAD

• Gloucester
• On-site
• £45,000 – £50,000 pa
• Mid-level
• Permanent

Support and maintain the effectiveness of a medical device manufacturer's QMS in line with ISO 13485, MDR and FDA requirements. Day-to-day work covers CAPA effectiveness, quality data and trend analysis, non-conformances, change control and complaint investigation, plus writing and updating procedures and work instructions.

ISO 13485 · FDA Quality System

• Cambridge
• Hybrid
• £35,000 – £45,000 pa
• Mid-level

Develops FPGA and embedded firmware for high-performance data acquisition and signal processing systems used in biomedical research products. Writes VHDL for FPGA functionality and C for low-level hardware control, integrating and debugging digital electronics across the full product lifecycle alongside hardware and software engineers.

AMD/Xilinx Vivado · Intel Quartus · USB +1

• Havant
• £50,000 – £60,000 pa
• Mid-level
• Permanent

Support the development and manufacture of biopharmaceutical and medical device products, working with design, product management and production teams. Duties include prototype builds, process validation, data analysis, resolving manufacturing issues and continuous improvement, with ERP systems used day to day.

ERP

• Stockton-on-Tees
• £40,000 – £46,000 pa

Plans, coordinates and documents process validation activities across NPI and manufacturing projects, preparing protocols, reports and technical evidence. Works with Engineering, Quality, Operations and customers on PPAP submissions, FMEAs and process flow diagrams to demonstrate manufacturing readiness in a regulated medical manufacturing environment.

• Cardiff
• On-site
• £40,000 – £50,000 pa

Owns process performance in a regulated medical device plant, analysing production data to improve OEE, yield, flow and cost. Works hands-on on the shop floor with operators and maintenance on fault-finding, machine trials, process validation, PFMEAs and Lean continuous improvement. Covers double day shifts with an on-call weekend rota.

Microsoft Excel · 2D CAD · 3D CAD +3

• Cardiff
• On-site
• £50,000 pa
• Mid-level
• Shift work

Owns a highly automated production line at a global medical device manufacturer, combining hands-on fault-finding, root cause investigation and continuous improvement to raise machinery reliability and cut downtime. Works on a two-shift rotation with weekend on-call, partnering with production, maintenance and quality teams on OEE, process validation and NPI.

Power BI · PLC · HMI +2

• 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,…

• Barnard Castle
• On-site
• £65,000 – £70,000 pa
• Mid-level · manages people

Leads a site maintenance department, overseeing planning and delivery of all engineering activities while driving a shift toward proactive maintenance. Manages employee relations, resource planning, shutdowns and CAPEX projects, tracking KPIs and SAP data to reduce downtime and improve machinery and processes.

SAP

• Abingdon
• £50,000 – £55,000 pa
• Lead

Leads a team of five production engineers to drive industrialisation, process improvement, and new product introduction within a regulated medical device environment. Focuses on evolving production systems through automation, Lean methodologies, and design-for-manufacture principles while ensuring quality, scalability, and regulatory compliance. Plays a central role in transitioning next-generation products from development into robust, efficient production.