Medical Technology Jobs

• London
• Hybrid · 2–3 days in office
• £95,200 – £142,800 pa
• Lead
• Contract

Builds and maintains the internal platform tooling that other engineering teams rely on, spanning Infrastructure as Code with OpenTofu, EKS and Helm, CI/CD automation, and observability with OpenTelemetry. Also supports AI agentic workflows and designs pragmatic fixes for developer productivity gaps, mentoring engineers across the organisation.

AWS · OpenTofu · EKS +3

• Heerlen, Netherlands
• €76,880 – €115,320 pa
• Lead

Senior individual contributor leading Customer Experience improvement across EMEA for a medical technology firm's Service & Repair organisation. Uses NPS, Voice of the Customer, journey data and operational metrics to identify root causes, then drives cross-functional initiatives, dashboards and executive reporting, partnering with digital transformation teams on self-service tools.

CRM · AI

• Maidenhead
• Hybrid
• Mid-level

Responsible for executing study-level activities including creating trial-specific documents, vendor oversight and compound training, plus country and regional oversight of local operational delivery. Aligns feasibility strategy, runs risk reviews, resolves trial issues and supports Health Authority inspections, mentoring new Trial Management team members.

Clinical Trial Management Systems (CTMS)

• Maidenhead
• Hybrid · 3 days in office
• Director · manages people

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and acts as product point of contact, with hybrid working requiring three days on site.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Coventry

Owns territory business plans and sales targets for electrophysiology products across West Midlands hospital accounts, driving catheter utilisation and capital sales to grow market share. Builds clinical and non-clinical customer relationships, manages tenders and local pricing, and executes EMEA marketing launches alongside regional sales and technical specialist colleagues.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint +1

• Beerse, Belgium
• Hybrid
• €82,000 – €141,450 pa
• Mid-level

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.

Company Core Data Sheet (CCDS) · United States Package Insert (USPI) · European Union Product Information (EUPI)

• Warsaw, Poland
• Hybrid
• €205,000 – €354,200 pa
• Mid-level

Leads the development, revision and maintenance of primary labeling documents such as 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.

Company Core Data Sheet (CCDS) · United States Package Insert (USPI) · EU Product Information (EUPI) +1

• Allschwil, Switzerland
• Hybrid
• Mid-level

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.

Company Core Data Sheet · United States Package Insert · EU Product Information

• Zug, Switzerland
• Hybrid
• Mid-level

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.

• Bern, Switzerland
• Hybrid
• Mid-level

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.

• Wokingham
• Mid-level · manages people

Leads Structural Heart market development across EMEA for intracardiac echocardiography solutions, managing a team of Ultrasound Clinical Account Specialists. Translates regional strategy into country-level growth plans, builds relationships with interventional cardiologists and hospital leaders, and drives adoption of ICE-guided workflows. Combines people leadership, business development and cross-functional execution with up to 60% travel.

AcuNav · NUVISION

• Issy-les-Moulineaux, France
• Mid-level · manages people

Leads EMEA Structural Heart market development, managing two Ultrasound Clinical Account Specialists and driving adoption of AcuNav and NUVISION intracardiac echocardiography solutions. Translates regional strategy into country growth plans, builds relationships with interventional cardiologists and hospital leaders, and oversees pipeline, forecasting and compliance across a matrixed organisation.

AcuNav · NUVISION

• Raritan, United States
• Hybrid · 3 days in office
• US$137,000 – US$235,750 pa
• Director · manages people

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and benefit-risk evaluations. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product SME for audits and health authority interactions.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Horsham, United States
• Hybrid · 3 days in office
• US$137,000 – US$235,750 pa
• Director · manages people

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product or process subject matter expert for audits and health authority interactions.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Titusville, United States
• Hybrid · 3 days in office
• US$137,000 – US$235,750 pa
• Director · manages people

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and evaluations. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with oversight of deliverables prepared by other team members.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint