Medical Technology Jobs

Johnson & Johnson MedTech · Breda, Netherlands · €68,600 – €119,600 pa

Oversees the end-to-end process for internal and external clinical data sharing requests, ensuring compliance with privacy standards and procedures. Manages vendors handling anonymisation and synthetisation, and acts as the primary contact for YODA Project requests, supporting external research teams using clinical study data.

Johnson & Johnson MedTech · Raynham, United States · US$122,000 – US$245,000 pa

Provides global strategic and operational leadership for environmental, health, safety and Process Safety Management programs, ensuring regulatory compliance and embedding risk-based safety practices into manufacturing operations. Partners with site leadership, engineering and operations on audits, investigations and corrective actions, and coaches leaders to strengthen safety culture across a regulated medtech business.

Johnson & Johnson MedTech · Warsaw, United States · US$122,000 – US$245,000 pa

Provides global strategic and operational leadership for environmental, health, safety and Process Safety Management programs, ensuring regulatory compliance and embedding risk-based safety practices into manufacturing. Partners with site leadership, engineering and operations on audits, investigations and corrective actions, and coaches leaders to strengthen safety culture across a highly regulated medtech environment.

Johnson & Johnson MedTech · Toronto, Canada · US$134,000 – US$184,000 pa

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.

Johnson & Johnson MedTech · Allschwil, Switzerland

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Acts as lead writer or point of contact for assigned programmes, planning and directing writing groups while coaching junior staff and managing direct reports. Involves cross-functional collaboration, regulatory guideline knowledge and departmental process improvement.

Johnson & Johnson MedTech · Leiden, Netherlands · €68,600 – €119,600 pa

Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports including hiring and performance discussions.

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

Leads regulatory medical writing for the Immunology therapeutic area, preparing and finalizing clinical documents and serving as lead writer or point of contact for assigned programs. Manages direct reports, sets objectives, mentors junior writers and oversees external contractors, while driving process improvements and cross-functional coordination.

Johnson & Johnson MedTech · Beerse, Belgium · €79,800 – €137,770 pa

Leads preparation and finalisation of clinical and regulatory documents for the Immunology therapeutic area within the Regulatory Medical Writing team. Acts as lead writer or point of contact for programmes, guides cross-functional teams, and manages, mentors and develops direct reports in medical writing.

Johnson & Johnson MedTech · Maidenhead

Supports Clinical Trial Management Solutions including CTMS, Site Payments and Access Provisioning, acting as liaison between business partners, IT and suppliers. Handles study build, system integrations, release management, user acceptance testing, end-user support and audits, while identifying automation, analytics and GenAI improvements. Requires deep clinical development and GCP knowledge.

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.

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 · 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 · Bern, 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 · 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 · 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.