Medical Technology Jobs

• Leeds
• Lead

Responsible for scenario planning, capacity planning, inventory management, and product deployment across multiple suppliers and brands. Drives continuous improvement through value stream mapping and builds complex statistical models to support master scheduling and S&OP integration. Works with MRP and ERP systems (SAP/JDE/APO/OMP) in a matrix environment.

SAP · JDE · APO +3

• Coventry

Owns territory business plans and sales targets for electrophysiology products across West Midlands hospital accounts, driving catheter utilisation and capital sales to grow market share. Builds clinical and non-clinical customer relationships, manages tenders and local pricing, and executes EMEA marketing launches alongside regional sales and technical specialist colleagues.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint +1

• Eindhoven, Netherlands
• Remote
• €52,800 – €79,200 pa

Regional product expert for Medtronic's ENT Head & Neck surgical portfolio across Western Europe, driving market development, clinical education and commercialisation. Partners with surgeons, distributors and sales teams to deliver training, lead product launches and build positioning and value propositions. Reports to the Marketing Director and works remotely.

• Madrid, Spain
• Remote
• €38,400 – €57,600 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 and working remotely.

• London

Leads the clinical launch and adoption of VELYS Spine robotics and navigation across UK spinal units, providing in-theatre case support and real-time troubleshooting during procedures. Delivers structured training to surgeons and theatre teams, drives utilisation and case volume growth, and acts as the clinical liaison between customers and internal Sales, Marketing, Medical Education and R&D teams. Field-based with high travel across priority UK sites.

VELYS Spine

• Leeds
• Entry level
• Internship

A 12-month student placement in the clinical research department, supporting international trials of medical technology products. The role involves administrative tracking and monitoring of high-profile studies, maintaining essential documents, data collection, and coordinating logistics from setup to completion, with exposure to cutting-edge clinical trials.

Microsoft Excel · Microsoft Word · Microsoft PowerPoint

• High Wycombe
• Hybrid · 3 days in office
• Entry level
• Internship

A 12-week summer internship in EMEA Global Regulatory Affairs within the Oncology therapeutic area, supporting the development of oncologic therapeutics across Phase I to III clinical studies. The intern joins a global matrixed team, contributes to cross-functional trial team activities, and conducts a research project on a topic impacting the regulatory function, presenting findings at a company-wide research symposium.

Microsoft Outlook · Microsoft Excel · Microsoft PowerPoint +5

• 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.