Medical Technology Jobs

• Madrid, Spain
• €56,100 – €97,635 pa
• Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) across West EMEA, translating regional strategy into country growth plans and account-level commercial execution. Manages a team of six EP ultrasound clinical specialists, partnering with local EP leaders, marketing, professional education and market access to drive procedure adoption, protect existing accounts and win new users. Combines commercial leadership with strategic account development, forecasting, pricing discipline and compliance across a complex matrix.

CARTOSOUND

• Lisbon, Portugal
• €56,100 – €97,635 pa
• Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) across West EMEA, translating regional strategy into country growth plans and account-level commercial execution. Manages a team of six EP ultrasound clinical specialists, partnering with local EP leaders, marketing, health economics and market access to drive adoption, protect existing accounts and win new users. Combines commercial leadership with strategic account development in a complex matrix.

CARTOSOUND

• Vienna, Austria
• €56,100 – €97,635 pa
• Lead · manages people

Lead the expansion of intracardiac echocardiography (ICE) across West EMEA, translating regional strategy into country growth plans and account-level commercial execution. Manage a team of six EP ultrasound clinical specialists while partnering with local EP leaders, marketing, professional education and market access to drive procedure adoption, protect existing accounts and win new users.

CARTOSOUND

• Madrid - Lafinca
• €56,100 – €97,635 pa
• Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) across West EMEA within Johnson & Johnson MedTech Electrophysiology, owning regional sales, procedure adoption and market share targets. Builds country growth plans with local EP teams, develops strategic accounts and manages a team of six ultrasound clinical specialists across a complex matrix. Combines commercial leadership with clinical enablement, pricing discipline and healthcare compliance.

CARTOSOUND

• High Wycombe
• Hybrid · 3 days in office
• Entry level
• Internship

A 12-week summer internship in EMEA Global Regulatory Affairs within the Oncology therapeutic area, supporting the development of oncologic therapeutics across Phase I to III clinical studies. The intern joins a global matrixed team, contributes to cross-functional trial team activities, and conducts a research project on a topic impacting the regulatory function, presenting findings at a company-wide research symposium.

Microsoft Outlook · Microsoft Excel · Microsoft PowerPoint +5

• Raritan, United States
• Hybrid
• US$122,000 – US$211,025 pa
• Lead

Shapes enterprise PLM architecture across MedTech, defining how product data, engineering change control, BOM configuration and lifecycle workflows evolve. Produces blueprints, reference patterns and design principles, guides platform simplification and reuse, and mentors architects while working with R&D, Quality, Regulatory and vendor partners.

Windchill · ThingWorx · Integrity +2

• Beerse, Belgium
• Hybrid
• Entry level
• Contract

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. Build and test prototypes on real GenAI platform workflows, publish results, and work with engineering partners to move validated methods into production.

OPA · Rego · Cedar +2

• Limerick, Ireland
• Hybrid
• Entry level
• Temporary

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered safeguards, publish results, and work with platform engineers to move validated methods into a GenAI platform.

OPA/Rego · Cedar

• Leiden, Netherlands
• Hybrid
• Entry level
• Temporary

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. Build and validate prototypes on real GenAI platform workflows, publish results, and work with engineering partners to move validated methods into production.

OPA · Rego · Cedar

• Maidenhead
• Hybrid
• Entry level
• Temporary

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. Build and test prototypes on real GenAI platform workflows, publish results, and work with engineering partners to move validated methods into production.

OPA · Rego · Cedar

• Leeds
• Entry level
• Internship

A 12-month student placement in the clinical research department, supporting international trials of medical technology products. The role involves administrative tracking and monitoring of high-profile studies, maintaining essential documents, data collection, and coordinating logistics from setup to completion, with exposure to cutting-edge clinical trials.

Microsoft Excel · Microsoft Word · Microsoft PowerPoint

• 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

• Blackpool
• Mid-level

Owns and optimises assigned manufacturing value streams to ensure safe, compliant and cost-effective production of medical devices. Provides technical leadership, directs complex process development and validation programmes (IQ, OQ, PQ), leads continuous improvement initiatives and mentors junior engineers while representing Engineering in governance and regulatory forums.

Siemens · Rockwell · HMI +1

• Leeds
• Hybrid
• Entry level
• Internship

Supports a Clinical Operations team in the day-to-day coordination of clinical studies, maintaining the Trial Master File (TMF/eTMF), tracking activities in CTMS, generating reports and distributing study supplies and regulatory documentation. A student placement offering hands-on exposure to clinical research processes and systems, working with study teams, project managers and site managers. Based in Leeds with flexibility to work remotely, though onsite working is preferred.

Microsoft Office · Microsoft Excel · Microsoft Word +4

• Allschwil, Switzerland
• Mid-level

Lead Pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery, while acting as a quality partner for the Office of the Chief Medical Officer. Drive digital transformation toward data-centric content and a robust qualification management system, managing timelines, risks, and audits across a matrixed organization.