Medical Technology Jobs

Johnson & Johnson MedTech · CZ005 Walterovo Namesti

Supports the Medical Affairs team on intraocular lens (IOL) proctoring and Medical Information requests, analysing surgical cases and calculations to optimise clinical outcomes. 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 · 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 · High Wycombe

A 12-month industry placement within the Integrated Data Analytics and Reporting function, specifically Clinical and Statistical Programming. The student applies SAS, R and Python to analyse trial data, build automation and AI-driven tools, and document solutions across disease areas, working alongside programming experts in a pharmaceutical research department.

Johnson & Johnson MedTech · Maidenhead

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance, and safety-native architecture. You will design reproducible experiments, prototype layered safeguards, publish results, and work with platform engineers to move validated methods into a GenAI platform.

Johnson & Johnson MedTech · Maidenhead

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 SOPs and local regulations. 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 · Limerick, Ireland

Lead a two-year postdoctoral research program on making agentic AI safe for pharmaceutical R&D, covering provable controls, adversarial assurance and safety-native architecture. Hands-on work prototyping and validating methods on real GenAI platform workflows, publishing results and handing validated approaches to engineering partners.