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Digital Test Specialist

The role involves defining and executing quality assurance strategies for digital and data products in a regulated medical device environment. Responsibilities include leading verification and validation, developing test automation, ensuring compliance with standards like IEC 62304 and ISO 14971, and establishing data quality controls across pipelines and cloud platforms. The specialist will act as a test authority, collaborating with engineering, regulatory, and clinical teams to embed quality throughout the product lifecycle.

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OrganOx

Oxford, United Kingdom

£33 – £35 pa Contract

Research Assistant in MedTech Translation (Fixed Term)

The role involves supporting translational research in bioelectronic devices by preparing and conducting experiments with in vitro neuronal and astrocyte cultures, integrating them with devices, and maintaining lab operations. The researcher will contribute to data collection, analysis, publication, and training others in cell culture techniques. Work takes place within a collaborative, interdisciplinary team focused on advancing MedTech applications.

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University of Cambridge

Cambridge, South East England, United Kingdom

Surgical Solutions Manager

The role involves supporting surgeons and theatre teams in hospitals by promoting and educating on Smith & Nephew's orthopaedic reconstruction technologies. You'll build clinical relationships, manage product inventory, support training, and drive adoption of innovative surgical solutions across the Oswestry and Stoke-on-Trent region. The position requires frequent travel and combines clinical engagement with commercial account management in a field-based setting.

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Smith & Nephew

Stoke-on-Trent, United Kingdom

£87,280 – £130,920 pa

Sr Prin Regulatory Affairs Spec

This role involves leading global regulatory strategies for AI-enabled medical technologies, managing complex product development programs and regulatory submissions across international markets. The specialist will guide cross-functional teams, ensure compliance with evolving regulations for digital health and AI/ML-based solutions, and proactively address regulatory risks. It emphasizes strategic leadership in cybersecurity, software, and AI-related regulatory affairs within a high-impact healthcare technology environment.

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Medtronic

London, United Kingdom

Hybrid Permanent Clearance Required

Sales Specialist - IGT D Coronary

This role involves driving sales of advanced cardiology and vascular imaging products across Scotland, combining technical expertise with strategic account management. The specialist will train existing customers, identify new business opportunities, and deliver clinical value propositions to healthcare providers. It requires deep product knowledge, CRM proficiency, and collaboration with marketing and clinical teams to support tender strategies and market expansion.

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Philips

Edinburgh, Alba / Scotland, United Kingdom

£45,000 – £49,000 pa

Regulatory Affairs Specialist - MedTech + More

Regulatory Affairs Specialist - MedTechA growing medical devices company in Cambridgeshire are currently in need of an experienced quality assurance and regulatory affairs specialist.This is an excellent opportunity for a QARA specialist to join this...

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Newton Colmore

Cambridge, Cambridgeshire, United Kingdom

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