Medical Technology Jobs

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.

Medtronic · Watford · £60,560 – £90,840 pa

Senior individual contributor leading customer experience improvement across EMEA for a Service & Repair customer care organisation. Uses NPS, Voice of the Customer, journey data and operational metrics to drive cross-functional initiatives, executive reporting and digital self-service adoption.

Medtronic · Cambridge · £36,000 – £54,000 pa

A 12-month structured development programme in cardiac electrophysiology, training early-career professionals to support Affera mapping and ablation procedures in hospital cath labs. Field-based across the Midlands, it combines clinical education, mentorship and hands-on procedure support, with progression into a Technical Consultant role on completion.

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 · Prague, Czech Republic · CZK 704,000 – CZK 1,135,050 pa

Supports end-to-end medical coding of clinical trial data, ensuring consistent, accurate and reproducible coding aligned with regulatory and industry standards. Maintains global thesauri and dictionary encoding systems (MedDRA, WHO Drug), handles coding specifications, quality reviews and sign-off, and advises cross-functional partners on coding issues.

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.

Medtronic · Dublin, Ireland

Leads the EMEA Service Marketing strategy for a global healthcare technology company, working across operating units and regional teams to develop service offerings and drive commercial growth. Combines strategic marketing, commercial planning, sales enablement and customer engagement, using market insights and competitive analysis to expand market share. Involves travel within the EMEA region.

Medtronic · Exeter · £41,200 – £61,800 pa

You will lead the integration of the HUGO RAS system into hospitals, developing program goals, surgeon and staff training plans, and driving technology adoption through change management. The role involves coaching clinical teams to self-sufficiency and coordinating with field service engineers to prepare operating rooms, with over 75% travel across the UK and Ireland.

Medtronic · Bristol · £41,200 – £61,800 pa

You will lead the integration of the HUGO RAS surgical robot into hospitals, developing program goals, surgeon and staff training plans, and driving technology adoption through change management. The role involves coaching clinical teams to self-sufficiency and coordinating with field service engineers, with over 75% travel across the UK and Ireland.