Medical Technology Jobs in Exeter

• Maidenhead

Field-based sales role covering the North East region, growing the breast implant and reconstruction device business across public and private secondary care. You own clinical and commercial relationships with plastic and oncoplastic breast surgeons, build account business plans, and lead customer education with support from marketing and professional education teams.

Oracle Customer Data Management (CDM)

• Hamburg, Germany
• €93,500 – €149,845 pa
• Mid-level

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.

Microsoft Office · Word · Excel +3

• Wokingham
• €93,500 – €149,845 pa
• Mid-level

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.

Microsoft Office · Microsoft Word · Microsoft Excel +3

• Machelen, Belgium
• €93,500 – €149,845 pa
• Mid-level

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.

Microsoft Office · Word · Excel +3

• 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

• Belgrade, Serbia
• Mid-level · manages people

Oversees local literature surveillance across 80+ territories, leading outsourced vendor operations and governance for global pharmacovigilance. Acts as business owner for controlled documents, policies and standards, driving standardisation and process improvement while partnering with cross-functional stakeholders across EMEA, Asia Pacific and other regions.

• Raynham, United States
• Hybrid
• US$140,000 – US$241,500 pa
• Lead

Acts as a procedural workflow architect, defining end-to-end surgical workflows across preoperative, intraoperative and postoperative care. Translates clinical, operational, usability and economic needs into procedural requirements and design inputs, partnering with R&D, clinical, regulatory and commercial teams. Requires workflow mapping, human factors and design tooling such as Figma, Miro and Polarion.

Adobe Illustrator · Photoshop · InDesign +7

• Warsaw, United States
• Hybrid
• US$140,000 – US$241,500 pa
• Lead

Acts as a procedural workflow architect defining end-to-end surgical workflows across preoperative, intraoperative and postoperative care, translating clinical, operational and usability needs into integrated procedural requirements. Partners with R&D, clinical, regulatory and commercial stakeholders to map current and future-state workflows and guide implant, instrument and digital solution development.

Adobe Illustrator · Photoshop · InDesign +7

• Palm Beach Gardens, United States
• Hybrid
• US$140,000 – US$241,500 pa
• Lead

Acts as a procedural workflow architect, defining end-to-end surgical workflows across preoperative, intraoperative and postoperative care and translating clinical, usability and economic needs into integrated procedural requirements. Partners with R&D, clinical, regulatory and commercial teams to map current and future-state workflows and guide development of implants, instruments, digital and service solutions.

Adobe Illustrator · Photoshop · InDesign +7

• 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

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

Leads strategic oversight and continuous improvement of local literature surveillance across 80+ territories, managing outsourced vendor partnerships and governance for global pharmacovigilance. Acts as business owner for controlled documents, policies and standards, driving standardisation, scalability and process improvement with cross-functional stakeholders across EMEA and Asia Pacific.

• Lisbon, Portugal
• €51,000 – €87,285 pa
• Mid-level · manages people

Leads strategic oversight and continuous improvement of local literature surveillance across 80+ territories, managing outsourced vendor partnerships and governance. Serves as business owner for controlled documents, policies and global standards, partnering with cross-functional stakeholders across EMEA and Asia Pacific to drive standardisation and operational excellence in pharmacovigilance.

• Maidenhead
• Mid-level · manages people

Oversees local literature surveillance across 80+ territories, leading outsourced vendor operations and governance to meet global pharmacovigilance obligations. Acts as business owner for controlled documents and standards, driving standardisation and process improvement while partnering with cross-functional stakeholders across EMEA, Asia Pacific and other regions.

• Neuss, Germany
• Mid-level · manages people

Oversees local literature surveillance across 80+ territories, leading outsourced vendor operations and ensuring compliant, timely pharmacovigilance monitoring. Acts as business owner for governance, controlled documents and global standards, partnering with EMEA and Asia Pacific stakeholders to drive standardisation and process improvement.

• 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.