Medical Technology Jobs

• West Chester, United States
• US$96,000 – US$155,250 pa
• Lead

Drive end-to-end supply chain improvements through value stream mapping and complex statistical modelling, covering master scheduling, capacity planning, scenario analysis and inventory management across multiple suppliers and brands. Integrate externally manufactured products into S&OP, advise External Operations management, and use MRP/ERP systems (SAP/JDE/APO/OMP), Excel and data visualisation tools to support decisions.

SAP · JDE · APO +3

• Raritan, United States
• US$96,000 – US$155,250 pa
• Lead

Owns end-to-end supply planning for an orthopaedics business, covering scenario planning, capacity and inventory management, product deployment and the annual business planning cycle. Builds complex statistical and simulation models in Excel and data-visualisation tools, working with MRP/ERP systems (SAP, JDE, APO, OMP) and driving continuous improvement through value stream mapping.

SAP · JDE · APO +3

• Milan, Italy
• Remote
• Director · manages people

Leads commercial growth and adoption of connected care and digital health solutions across Western European hospital systems, negotiating multi-year enterprise agreements and guiding product launches. Manages a growing team and works with clinical, IT and executive stakeholders on interoperability and data integration. Remote with around 70% regional travel.

HL7 · FHIR · APIs +2

• 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

• Maidenhead
• Hybrid
• Mid-level

Responsible for executing study-level activities including creating trial-specific documents, vendor oversight and compound training, plus country and regional oversight of local operational delivery. Aligns feasibility strategy, runs risk reviews, resolves trial issues and supports Health Authority inspections, mentoring new Trial Management team members.

Clinical Trial Management Systems (CTMS)

• Blackpool
• Mid-level

Owns and optimises assigned manufacturing value streams to ensure safe, compliant and cost-effective production of medical devices. Provides technical leadership, directs complex process development and validation programmes (IQ, OQ, PQ), leads continuous improvement initiatives and mentors junior engineers while representing Engineering in governance and regulatory forums.

Siemens · Rockwell · HMI +1

• 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.

• Allschwil, Switzerland
• Mid-level

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

• 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.

• 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.