Medical Technology Jobs

• Vienna, Austria
• €56,100 – €97,635 pa
• Lead · manages people

Lead the expansion of intracardiac echocardiography (ICE) across West EMEA, translating regional strategy into country growth plans and account-level commercial execution. Manage a team of six EP ultrasound clinical specialists while partnering with local EP leaders, marketing, professional education and market access to drive procedure adoption, protect existing accounts and win new users.

CARTOSOUND

• Maidenhead
• Entry level
• Internship

Supports the Local Trial Manager and Site Manager with document management and administrative tasks across trial start-up, execution and close-out, ensuring compliance with SOPs and local regulations. Also contributes to process improvement, training and mentoring of other CTAs, partnering with Business Operations, study teams and stakeholders such as Finance and Procurement.

Microsoft Word · Microsoft PowerPoint · Microsoft Excel

• Newport
• £52,000 pa

Field Service Engineer, Medical Diagnostic SystemsOverall Earnings £65,000Basic Salary Up To £52,000Door To Door OvertimeOn Call Allowance10% BonusCompany Car (Electric Or Hybrid)PensionHealthcareLife InsurancePhone, LaptopHolidaysThe Role – Field Service Engineer, Medical Diagnostic SystemsThis market leader seeks to recruit a technically motivated…

• Taunton
• £52,000 pa

Servicing, installing, repairing and calibrating sophisticated laboratory diagnostics systems in pathology departments, NHS labs and clinical chemistry environments, including flow cytometry and cell separation products at customer sites. Requires a field service or technical support background in electronics or electro-mechanical equipment, with customer-facing confidence and an ONC/HNC or above.

Flow Cytometry · Cell Separation · Microscopy +4

• 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.

• 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

• 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
• Entry level

Two-year graduate development programme comprising four six-month rotations across functions such as process engineering, continuous improvement, production operations, R&D and quality. Graduates own real projects supporting new product and process introductions, testing and continuous improvement, with mentoring and cross-functional networking in a medical devices environment.

Microsoft Office · CAD

• 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

• 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.

• 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.