Medical Technology Jobs

• London
• Remote
• £44,000 – £66,000 pa

Regional product expert for the ENT/Head & Neck surgical portfolio across Western Europe, driving market development, clinical education and product launches. Partners with surgeons, distributors and sales teams to build adoption and inform strategy, reporting to the Marketing Director in a remote role.

• Cambridge
• £36,000 – £54,000 pa
• Entry level

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.

Affera Mapping Technology

• CZ005 Walterovo Namesti
• Hybrid
• Mid-level
• Permanent

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.

• Rungis, France
• Hybrid
• Mid-level
• Permanent

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.

• Peterborough
• Hybrid
• Senior

Field-based role owning a strategic orthopaedic revision territory from the M1 corridor to the East of England, supporting complex surgical cases in theatre and building relationships with surgeons and theatre teams. Combines clinical expertise with commercial account planning, tenders and product introductions, including advanced technologies such as robotics.

Robotics

• London
• Hybrid
• Contract

Repair and maintain medical devices, performing preventative maintenance for service-contract customers and precision instrument servicing under a microscope, including sharpening surgical instruments. The role involves managing personal inventory, supporting the wider Service Engineering team, and building relationships with hospital staff and internal sales teams, with training to certify across multiple product franchises.

• Beerse, Belgium
• €81,400 – €140,530 pa
• Mid-level

Leads Pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery. Acts as a quality partner for the Innovative Medicines Office of the Chief Medical Officer, linking business partners, quality groups, and governance while supporting a digital transformation toward data-centric content and qualification management. Manages timelines, risks, and audits or inspections.

• Horsham, United States
• US$105,000 – US$181,700 pa
• Mid-level

Lead pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery. Act as a quality partner linking business partners, quality groups, and governance, supporting a digital transformation toward data-centric content and qualification management. Manage timelines, risks, and audits within a matrix organization.

ISO 9001

• Raritan, United States
• US$105,000 – US$181,700 pa
• Mid-level

Lead pharmacovigilance process and training projects, including process development, mapping, and training qualification and delivery, while acting as a quality partner between business, quality, and governance groups. Support a digital transformation roadmap toward data-centric content and a qualification management system, managing timelines, risks, and audits.

• Titusville, United States
• US$105,000 – US$181,700 pa
• Mid-level

Lead pharmacovigilance process and training projects, including process development, mapping, and qualification delivery, while acting as a quality partner to the Office of the Chief Medical Officer. Drive digital transformation toward data-centric content and qualification management, managing risks, timelines, and audits across a matrixed life sciences organization.

• Beerse, Belgium
• €79,800 – €137,770 pa
• Mid-level · manages people

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.

• Leiden, Netherlands
• €68,600 – €119,600 pa
• Mid-level · manages people

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.

• Toronto, Canada
• US$134,000 – US$184,000 pa
• Mid-level · manages people

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.

• Spring House, United States
• US$117,000 – US$201,250 pa
• Mid-level · manages people

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.

• Allschwil, Switzerland
• Mid-level · manages people

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.