Medical Technology Jobs

Director, Procurement Technology & Enablement

Lead the strategy and delivery of a global, data-driven Source-to-Pay (S2P) ecosystem, owning the technology roadmap, data governance, and digital transformation across procurement. Drive adoption, change management, and analytics capabilities while partnering with IT, Finance, and business leaders to enable measurable business outcomes in a regulated, global environment.

Smith & Nephew United States US$220,000 – US$240,000 pa

On-site Permanent

Director, Procurement Technology & Enablement

Leads the end-to-end procurement technology strategy and digital transformation for a global, regulated enterprise, focusing on building a modern, data-driven Source-to-Pay (S2P) ecosystem. Drives platform governance, data analytics, process simplification, and user adoption across sourcing, contracting, purchasing, and supplier management. Partners with IT, Finance, and business stakeholders to deliver measurable business outcomes through technology innovation and change leadership.

Smith & Nephew US$220,000 – US$240,000 pa

On-site Permanent

Sales Representative

The Sales Representative role involves developing and maintaining Medtronic's Embolisation, Deep Venous, and Peripheral Vascular portfolios with existing and new customers. Responsibilities include analyzing the marketplace, building sales strategies, and providing technical and clinical support to healthcare professionals.

Medtronic London, United Kingdom £43,200 – £64,800 pa

On-site Permanent

Principal Embedded Software Engineer - 6-Month

As a Principal Embedded Engineer, you will work on expanding the feature set of existing medical devices and ensuring the codebase is maintainable. You will collaborate with multidisciplinary teams to develop and productize custom computing devices, optimize performance, and ensure robust and secure software for medical-grade systems.

Medtronic London, United Kingdom

On-site Contract

Senior Supplier Assurance Engineer

The Senior Supplier Assurance Engineer leads supplier quality activities, ensuring compliance with global regulations and internal QMS processes. Key responsibilities include supplier qualification, performance monitoring, and continuous improvement, with a focus on maintaining high-quality standards across the supply chain.

OrganOx Oxford, United Kingdom

On-site Permanent Flexible

Electronics Design Engineer

The Electronics Design Engineer will design, develop, and support electronics systems for OrganOx’s medical devices, ensuring compliance with regulatory and safety standards. Responsibilities include full lifecycle electronics design, from concept to manufacturing, with a focus on reliability, safety, and manufacturability.

OrganOx Oxford, United Kingdom

On-site Permanent

Sales Specialist - IGT D Coronary

This role involves driving sales of cardiology and vascular medical equipment across Scotland by building relationships with healthcare customers, delivering product training, and identifying new business opportunities. The specialist will work independently from a home base, combining technical knowledge with strategic sales planning to support clinical customers and meet commercial targets. A focus on customer satisfaction, compliance, and collaboration with marketing and stakeholders is key to success.

Philips Edinburgh, Alba / Scotland, United Kingdom

Hybrid Permanent Clearance Required

Clinical Application Specialist - CV

This role involves training healthcare professionals on Philips' cardiovascular devices, ensuring successful clinical adoption, and supporting sales through technical expertise and product demonstrations. You will work closely with key opinion leaders and organize events to showcase Philips' solutions in the image-guided therapy market.

Philips Rushmoor, GU14 7JT, United Kingdom

Remote Permanent Clearance Required

Quality Officer (GDP) - Midlands

This role involves ensuring compliance with Good Distribution Practise (GDP) and quality standards across operational processes. The Quality Officer will manage QA documentation, lead deviation and CAPA processes, support audits, and maintain the Quality Management System. The position requires strong organisational skills and experience in regulatory compliance within a healthcare or logistics environment.

Adecco United Kingdom £37,000 – £42,000 pa

Hybrid Permanent

AWS DevOps Engineer (Bioinformatics Experience)

AWS DevOps Engineer (Bioinformatics Sector)Oxford (1 day per month in office).£75-90k + Benefits.- This role cannot offer Visa Sponsorship.- To apply for this role you must have experience working in the Bioinformatics / Life Sciences / Genomics / BioTech sector.Your...

HAYS Specialist Recruitment Oxfordshire, United Kingdom £75,000 – £90,000 pa

Design Assurance Engineer - Medical Devices - Cambridge

The role involves leading design assurance and quality activities for medical devices, including authoring and reviewing design documentation, managing Design History Files (DHF), and ensuring compliance with ISO 14971 and other regulatory standards. The engineer will actively participate in design reviews and work within a QMS framework to support product development in a high-tech environment.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Electronic System Engineer

Electronic System EngineerNewcastle Upon Tyne, United KingdomSalary: CompetitiveJackson Hogg is delighted to be working with a leading diagnostics business which is scalng up it's engineering team due to new international investment. This is for a dynamic electronics engineer who can...

Jackson Hogg Newcastle upon Tyne, Tyne & Wear, NE1 4JA, United Kingdom £40,000 – £55,000 pa

Senior Regulatory Affairs Specialist

This role involves leading regulatory strategy and compliance for medicinal products, medical devices, and cosmetics across the UK and Ireland. The specialist will manage submissions, support product launches, ensure compliance with MHRA and HPRA requirements, and provide regulatory guidance across the organisation, with a focus on post-Brexit regulatory pathways and lifecycle management.

GI Group Euston, London, NW1 2EA, United Kingdom £75,000 pa

Hybrid Contract

Regulatory Affairs Specialist

This role involves maintaining regulatory compliance for medical devices by managing technical documentation, product registrations, and post-market surveillance activities. The specialist will work independently in an SME setting, ensuring adherence to UK and EU regulations including MDR, MDD, and UKCA. Responsibilities include updating clinical evaluations, supporting audits, and managing documentation with a focus on accuracy and efficiency.

ProTech Recruitment Ltd Hertford, Hertfordshire, United Kingdom £35,000 – £40,000 pa

Hybrid Permanent Part-time

Regulatory Affairs Specialist - 6074

Manages the preparation and delivery of regulatory submissions to health authorities across multiple markets, coordinating timelines, translations, and document builds. Acts as a subject matter expert on dossier types and eCTD standards while mentoring colleagues and resolving submission-related issues. Focuses on improving efficiency through reuse of submission content across regions.

Talentmark Sandwich, Kent, United Kingdom £24 – £26 ph

Hybrid Contract Clearance Required