Medical Technology Jobs

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.

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 · 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 · High Wycombe

Supports the Local Trial Manager and Site Manager with document management and administrative tasks across trial start-up, execution and close-out, ensuring compliance with GCO SOPs and local regulatory requirements. Also contributes to process improvement, training and mentoring of other CTAs, partnering with Business Operations, study teams and stakeholders such as Finance and Procurement.

Johnson & Johnson MedTech · Espoo, Finland

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 healthcare professionals with post-operative outcome analysis and new product introductions. Home-office based with up to 20% travel, reporting to the Associate Director of Clinical Services.

Johnson & Johnson MedTech · Paris, France

Supports the Medical Affairs team on intraocular lens (IOL) proctoring and Medical Information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of J&J products. Provides clinical expert support to HCPs, manages MIR responses within four days, and produces performance statistics with Product Safety, Marketing and R&D. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · IE009 Janssen Cilag Ltd

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 · 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 · Dublin, Ireland

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Provides clinical guidance to healthcare professionals, generates MIR statistics reports, and collaborates with Product Safety, Marketing and R&D. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Milan, Italy

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Manages MIR responses within four days, produces performance statistics, and assists hospitals with sub-optimal outcomes. Home-office based with up to 20% travel, working closely with Product Safety, Marketing, R&D and Commercial teams.