Medical Technology Jobs

• Manchester
• On-site
• £43,200 – £64,800 pa

Field-based role covering the North West, providing clinical and technical support to electrophysiologists, cardiac physiologists and cath lab teams during cardiac ablation procedures using Cryo, PulseSelect and Affera therapies. Involves procedural troubleshooting, product and therapy training, and supporting installations and launches alongside sales and marketing to drive therapy adoption in assigned accounts.

Cryo · PulseSelect · Affera

• Milan, Italy
• €61,600 – €92,400 pa
• Senior

Defines and executes pricing strategy across a product portfolio and customer segments, analysing pricing trends, diagnostics and levers to hit operating unit objectives. Reviews key tenders and deals, monitors compliance, and works with Western Europe, Japan, Australia/New Zealand and global teams to embed pricing as a strategic profit lever.

Excel

• Espoo, Finland
• Hybrid
• Mid-level
• Permanent · Flexible

Supports intraocular lens proctoring and medical information requests to ensure optimal clinical outcomes, analysing sub-optimal results and clinic workflow factors. Manages MIR responses within four days, generates statistics reports, and assists healthcare professionals with post-operative outcome analysis and new product introductions. Home-office based with up to 20% travel, reporting to the Associate Director of Clinical Services.

• Pomezia, Roma, Italy
• Hybrid
• Mid-level
• Permanent

Supports intraocular lens proctoring and medical information requests, analysing surgical cases and sub-optimal outcomes to optimise clinical use of ophthalmic products. Handles MIR responses within four days, produces statistics reports, and assists HCPs with post-operative analysis and new product introductions. Home-office based with up to 20% travel across EMEA.

• UK - Field
• Contract

Repair and maintain medical devices, performing preventative maintenance for service-contract customers and precision instrument servicing under a microscope. The role involves inventory management, customer and hospital staff relationships, and completing certification across multiple product franchises, with a company vehicle provided for field-based visits.

Smith+Nephew Equipment

• Melton, UK
• On-site
• Director · manages people

Leads a major multi-year manufacturing transformation across the Hull and Melton sites, combining a legacy facility with a newly built one. Defines the future operating model, embeds lean management systems and tiered accountability, and coaches senior leaders and frontline teams to build a sustainable continuous improvement culture within a global Operational Excellence network.

• 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.

• 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)

• 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.

• High Wycombe
• Hybrid
• Mid-level

Leads the development, revision and maintenance of primary labeling documents such as the Company Core Data Sheet, US Package Insert and EU Product Information for assigned compounds. Advises on labeling content, processes and timelines, resolves labeling issues and contributes to global labeling strategy and continuous process improvement within a matrix team.

Company Core Data Sheet · United States Package Insert · EU Product Information