Medical Technology Jobs

• Machelen, Belgium
• €93,500 – €149,845 pa
• Mid-level

Field-based Medical Affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Involves building KOL relationships, managing investigator-initiated studies, providing scientific and HEOR support, reviewing promotional materials, and representing the company at conferences. Requires close cross-functional work with Clinical, Regulatory, Marketing and Market Access teams.

Microsoft Office · Word · Excel +3

• Prague, Czech Republic
• Hybrid
• CZK 704,000 – CZK 1,135,050 pa
• Mid-level

Supports end-to-end medical coding of clinical trial data, ensuring consistent, accurate and reproducible coding aligned with regulatory and industry standards. Maintains global thesauri and dictionary encoding systems (MedDRA, WHO Drug), handles coding specifications, quality reviews and sign-off, and advises cross-functional partners on coding issues.

MedDRA · WHODrug

• Dublin, Ireland
• Mid-level

Leads the EMEA Service Marketing strategy for a global healthcare technology company, working across operating units and regional teams to develop service offerings and drive commercial growth. Combines strategic marketing, commercial planning, sales enablement and customer engagement, using market insights and competitive analysis to expand market share. Involves travel within the EMEA region.

• Eindhoven, Netherlands
• Remote
• €52,800 – €79,200 pa

Regional product expert for Medtronic's ENT Head & Neck surgical portfolio across Western Europe, driving market development, clinical education and commercialisation. Partners with surgeons, distributors and sales teams to deliver training, lead product launches and build positioning and value propositions. Reports to the Marketing Director and works remotely.

• High Wycombe
• Hybrid
• 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 · United States Package Insert · EU Product Information

• Leiden, Netherlands
• Hybrid
• €64,500 – €104,535 pa
• Senior

Operational leader driving regulatory program management for the Immunology portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates Global Regulatory Team meetings, leads submissions and health authority meeting planning, and champions process and system rollouts within the RPM department.

Veeva · Microsoft Project · Planisware

• Allschwil, Switzerland
• Hybrid
• Senior

Operational leader driving regulatory program management for the Immunology portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates health authority meeting planning, worldwide submissions and marketing applications while leading change management for new processes and systems across the RPM team.

Veeva · Microsoft Project · Planisware

• Beerse, Belgium
• Hybrid
• €74,000 – €117,530 pa
• Senior

Operational leader driving regulatory program management for the Immunology portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates health authority meeting planning, worldwide submissions and marketing applications, while leading change management and process improvements across the RPM department.

Veeva · Microsoft Project · Planisware

• Ringaskiddy, Ireland
• Hybrid
• €64,300 – €102,925 pa
• Senior

Operational leader driving regulatory program management for the Immunology portfolio, translating global regulatory strategy into executable plans and coordinating cross-functional teams. Facilitates health authority meetings, worldwide submissions and marketing applications, while leading change management and process improvements within the RPM department.

Veeva · Microsoft Project · Planisware

• Maidenhead
• Hybrid
• Senior

Operational leader driving process improvement and change management within a Regulatory Program Management team, supporting global regulatory strategy for the Immunology portfolio. Facilitates cross-functional teams, translates regulatory strategy into executable plans, and leads operational execution of marketing applications and health authority meetings. Hybrid role with up to 10% international travel.

Planisware · Veeva · Microsoft Project

• Raritan, United States
• Hybrid
• US$117,000 – US$201,250 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 matrixed regulatory team.

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

• Horsham, United States
• Hybrid
• US$117,000 – US$201,250 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 matrixed regulatory affairs team.

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

• Titusville, United States
• Hybrid
• US$117,000 – US$201,250 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, timelines and scientific integrity, resolves labeling issues, and contributes to global labeling strategy and continuous process improvement within a matrix team.

Document Management Systems

• 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