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 · 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.

Smith & Nephew · Wrexham

Field-based clinical sales role covering North Wales and the Midlands, acting as the go-to expert for complex wound care within the Advanced Wound Management portfolio. Involves hands-on clinical support, education and relationship building with community healthcare professionals, guiding decision makers and strengthening advocacy for therapies across the territory.

Johnson & Johnson MedTech · Brussels, Brussels-Capital Region, Belgium

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Provides clinical guidance to healthcare professionals, tracks MIR statistics, and collaborates with Product Safety, Marketing and R&D on new product introductions. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Rungis, France

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Manages MIR responses within four days, produces performance statistics, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · GB019 Bessemer

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Provides expert clinical guidance to healthcare professionals, manages MIR responses within four days, and produces performance reports with Product Safety, Marketing and R&D. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Oslo, Norway

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. Handles MIR responses within four days, produces statistics reports, 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 · Pratica di Mare, Italy

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. Home-office based with up to 20% travel, reporting to the Associate Director of Clinical Services.

Johnson & Johnson MedTech · Copenhagen, Denmark

Supports the Medical Affairs team on intraocular lens (IOL) proctoring and Medical Information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical results. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Stockholm, Sweden

Supports the Medical Affairs team for intraocular lenses, analysing surgical cases and calculations, managing medical information requests within four days, and helping clinicians optimise post-operative outcomes. Works closely with Product Safety, Marketing, R&D and Commercial on clinical performance reporting and new product introductions, with home-office working and up to 20% travel.

Johnson & Johnson MedTech · Pomezia, Roma, Italy

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · London

Supports the Medical Affairs team with intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise product use. Provides clinical expert support to healthcare professionals on post-operative outcomes, new product introductions, demos and clinical studies, working closely with Product Safety, Marketing, R&D and Commercial. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Limerick, Ireland

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and post-operative outcomes to optimise clinical results. Collaborates with product safety, marketing, R&D and commercial teams, providing expert support to healthcare professionals and internal customers on new product introductions. Home-office based with up to 20% travel across EMEA.

Johnson & Johnson MedTech · Raritan, United States · US$137,000 – US$235,750 pa

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare regulatory safety analyses and benefit-risk evaluations. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product SME for audits and health authority interactions.

Johnson & Johnson MedTech · Horsham, United States · US$137,000 – US$235,750 pa

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, chairs proactive safety data reviews, and acts as product or process subject matter expert for audits and health authority interactions.