Medical Technology Jobs

• High Wycombe
• Mid-level

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

• 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.

• Watford
• £37,600 – £56,400 pa

Field-based role servicing and repairing a portfolio of medical technologies across ENT, Acute Care & Monitoring, Cranial & Spinal and Surgical Innovations. You perform installation, preventive maintenance and troubleshooting at hospitals, build relationships with Clinical Engineering and EBME teams, and support service contract renewals. Around 50-75% travel within the Manchester territory.

Computerized Maintenance Management Systems

• Bristol
• £55,040 – £82,560 pa

Field-based territory role supporting the Structural Heart Operating Unit across the Southwest, covering TAVI (Evolut) and TPV (Melody, Harmony) portfolios. Combines territory sales, account and therapy development, clinical and cath lab procedural support, training, and consignment inventory management, working with clinicians, procurement and referral partners across Bristol, Oxford, Derriford, Cardiff and Swansea.

Evolut · Melody · Harmony

• Zuchwil, Switzerland
• Senior · manages people

Accountable technology leader for the EMEA Deliver domain, owning the regional logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances transformation delivery with operational reliability, cybersecurity, compliance and lifecycle governance, while governing 3PL and vendor technology obligations. Leads a multi-country team and partners across a complex global matrix.

ERP · WMS · WCS/WES +4

• Blackpool
• Senior · manages people

Accountable technology leader for the EMEA Deliver domain, owning the multi-year logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances transformation delivery with operational reliability, cybersecurity, compliance and lifecycle governance, while leading a team and governing 3PL and vendor technology relationships.

ERP · WMS · WCS/WES +4

• Ringaskiddy, Ireland
• Senior · manages people

Accountable technology leader for the EMEA Deliver domain, owning the regional logistics technology roadmap across ERP, WMS, WCS/WES, TMS, warehouse automation and partner integrations. Balances transformation delivery with operational reliability, lifecycle governance, cybersecurity and 3PL vendor oversight, while leading a multi-country team and managing portfolio budgets and benefits realisation.

ERP · WMS · WCS/WES +4

• Leeds
• Senior

Hands-on role performing verification and investigational testing of orthopedic implants and instrumentation, developing test methods, fixtures and protocols for regulatory submissions. Works closely with R&D and Quality, contributes to design and process FMEAs, and leads departmental work instructions and audit support.

Load Cells · LVDT · Strain Gages +5

• Wokingham

Field-based clinical and technical role supporting electrophysiology procedures across the South UK, covering the South Coast, Oxford and surrounding areas. You will provide expert procedural support for the CARTO 3 Mapping System, ablation catheters and related EP solutions, train and educate hospital staff, and help drive technology adoption and account growth alongside commercial colleagues.

CARTO 3 Mapping System · Ablation Catheters

• Maidenhead
• Hybrid · 3 days in office
• Director · manages people

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, conducts proactive safety data reviews, and acts as product point of contact, with hybrid working requiring three days on site.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Prague, Czech Republic
• Hybrid
• CZK 704,000 – CZK 1,135,050 pa
• Mid-level

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.

MedDRA · WHODrug

• Maidenhead
• 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 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.

• 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.