65 jobs
Johnson & Johnson MedTech Blackpool
Two-year graduate development programme comprising four six-month rotations across functions such as process engineering, continuous improvement, production operations, R&D and quality. Graduates own real projects supporting new product and process introductions, testing and continuous improvement, with mentoring and cross-functional networking in a medical devices environment.
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 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 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 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 Hamburg, Germany €93,500 – €149,845 pa
Field-based medical affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Builds relationships with key opinion leaders, oversees investigator-initiated studies, reviews promotional materials, and provides scientific and HEOR support to cross-functional teams. Requires frequent conference attendance and up to 50% travel.
Johnson & Johnson MedTech Wokingham €93,500 – €149,845 pa
Field-based Medical Affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Builds relationships with key opinion leaders, supports investigator-initiated studies, reviews promotional materials, and provides scientific and HEOR support to cross-functional teams. Requires frequent conference attendance and up to 50% travel.
Johnson & Johnson MedTech Machelen, Belgium €93,500 – €149,845 pa
Field-based Medical Affairs role supporting Shockwave Medical's cardiovascular portfolio across Europe. Involves building KOL relationships, managing investigator-initiated studies, providing scientific and HEOR support, reviewing promotional materials, and representing the company at conferences. Requires close cross-functional work with Clinical, Regulatory, Marketing and Market Access teams.
Johnson & Johnson MedTech High Wycombe
Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection/submission readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving quality risk monitoring reviews, supporting CAPA plans, and leading inspection readiness and mock inspections with cross-functional teams.
Johnson & Johnson MedTech Maidenhead
Leads preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects covering content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves mentoring junior writers, overseeing external contractors, and driving departmental process improvements.
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 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 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 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 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.
