Medical Technology Jobs

Medtronic · Brussels, Brussels, Belgium · €77,600 – €116,400 pa

Delivers technical and clinical training on the Hugo RAS robotic surgery platform to surgeons, first assistants and OR staff across General Surgery, Urology and Gynaecology, running lab sessions and hands-on workshops at a Belgian training centre. Requires fluency in Portuguese and English and involves around 75% travel, working closely with sales, clinical and medical affairs teams.

Medtronic · Watford · £52,000 – £78,000 pa

Field-based clinical and technical expert supporting Cardiac Rhythm Management device implants, follow-up procedures and programming in catheterisation labs and operating theatres across London and the South East. Delivers training and education to physicians, physiologists and nurses, troubleshoots device issues, and works with sales and marketing to drive therapy adoption. Combines clinical expertise with customer-facing procedural support and frequent territory travel.

Johnson & Johnson MedTech · IE006 Airton

Supports the Medical Affairs team with intraocular lens proctoring and Medical Information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of J&J products. Collaborates with Product Safety, Marketing, R&D and Commercial on MIR statistics and clinical performance, and assists HCPs with post-operative outcome analysis and new product introductions. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Roden, Netherlands

Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists HCPs with post-operative outcome analysis. Provides clinical expert support for new product introductions, demos and clinical studies, working home-office based with up to 20% travel.

Johnson & Johnson MedTech · Allschwil, Switzerland

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.

Johnson & Johnson MedTech · Beerse, Belgium · €74,000 – €117,530 pa

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.

Johnson & Johnson MedTech · Ringaskiddy, Ireland · €64,300 – €102,925 pa

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.

Johnson & Johnson MedTech · Maidenhead

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.

Johnson & Johnson MedTech · Raritan, United States · US$117,000 – US$201,250 pa

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.

Johnson & Johnson MedTech · Horsham, United States · US$117,000 – US$201,250 pa

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.

Johnson & Johnson MedTech · Titusville, United States · US$117,000 – US$201,250 pa

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.

Johnson & Johnson MedTech · Beerse, Belgium · €82,000 – €141,450 pa

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.

Johnson & Johnson MedTech · Warsaw, Poland · €205,000 – €354,200 pa

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.

Johnson & Johnson MedTech · Allschwil, Switzerland

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.

Johnson & Johnson MedTech · Zug, Switzerland

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.