Medical Technology Jobs

• Madrid, Spain
• €68,400 – €108,790 pa
• Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) in electrophysiology across West EMEA, translating regional strategy into country growth plans and account-level execution. Manages a team of six EP ultrasound clinical specialists while partnering with country commercial, marketing, education and market access teams to protect, grow and win accounts. Combines commercial leadership, strategic account development and compliance governance in a complex matrix.

CARTOSOUND

• London
• Lead · manages people

Leads the expansion of intracardiac echocardiography (ICE) in electrophysiology 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 country EP leaders, marketing, health economics and professional education to drive adoption, protect the installed base and win new accounts.

CARTOSOUND

• Beerse, Belgium
• €81,400 – €140,530 pa
• Mid-level · manages people

Leads strategic oversight and continuous improvement of local literature surveillance across 80+ territories, managing outsourced vendor partnerships and governance for global pharmacovigilance. Acts as business owner for controlled documents, policies and standards, driving standardisation, scalability and process improvement with cross-functional stakeholders across EMEA and Asia Pacific.

• Lisbon, Portugal
• €51,000 – €87,285 pa
• Mid-level · manages people

Leads strategic oversight and continuous improvement of local literature surveillance across 80+ territories, managing outsourced vendor partnerships and governance. Serves as business owner for controlled documents, policies and global standards, partnering with cross-functional stakeholders across EMEA and Asia Pacific to drive standardisation and operational excellence in pharmacovigilance.

• Maidenhead
• Mid-level · manages people

Oversees local literature surveillance across 80+ territories, leading outsourced vendor operations and governance to meet global pharmacovigilance obligations. Acts as business owner for controlled documents and standards, driving standardisation and process improvement while partnering with cross-functional stakeholders across EMEA, Asia Pacific and other regions.

• Neuss, Germany
• Mid-level · manages people

Oversees local literature surveillance across 80+ territories, leading outsourced vendor operations and ensuring compliant, timely pharmacovigilance monitoring. Acts as business owner for governance, controlled documents and global standards, partnering with EMEA and Asia Pacific stakeholders to drive standardisation and process improvement.

• 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.

• High Wycombe
• Mid-level

Lead Pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery, while acting as a quality partner to the Innovative Medicines Office of the Chief Medical Officer. Drive digital transformation toward data-centric content and a qualification management system, managing timelines, risks, and audits within a matrixed life sciences environment.

• Beerse, Belgium
• €81,400 – €140,530 pa
• Mid-level

Leads Pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery. Acts as a quality partner for the Innovative Medicines Office of the Chief Medical Officer, linking business partners, quality groups, and governance while supporting a digital transformation toward data-centric content and qualification management. Manages timelines, risks, and audits or inspections.

• Horsham, United States
• US$105,000 – US$181,700 pa
• Mid-level

Lead pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery. Act as a quality partner linking business partners, quality groups, and governance, supporting a digital transformation toward data-centric content and qualification management. Manage timelines, risks, and audits within a matrix organization.

ISO 9001

• Raritan, United States
• US$105,000 – US$181,700 pa
• Mid-level

Lead pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery, while acting as a quality partner between business, quality, and governance groups. Support a digital transformation roadmap toward data-centric content and a qualification management system, managing timelines, risks, and audits.

• Titusville, United States
• US$105,000 – US$181,700 pa
• Mid-level

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

• Maidenhead
• Entry level

Field-based clinical and technical support role covering the Electrophysiology portfolio, spending 80%+ of time with customers supporting AF and CTI procedures and building CARTO hardware, software and HD mapping expertise. Works within a POD alongside Technical Specialists and Sales to drive case coverage, customer education and account growth while completing a structured training pathway.

CARTO · CARTOSOUND · Axonify +1

• Maidenhead
• Hybrid · 3 days in office
• Senior

Executes analytical risk-based monitoring activities across multiple complex clinical trials, reviewing site and subject-level data to detect early risks to data quality, participant safety and compliance. Works closely with Site Managers and Central Monitoring Managers, using data visualisation and reporting tools to guide site prioritisation and engagement.

• Toronto, Canada
• US$134,000 – US$184,000 pa
• Mid-level · manages people

Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned programmes, planning and directing writing groups, mentoring junior writers and overseeing external contractors. Also manages direct reports, setting objectives and running performance and development discussions.