Medical Technology Jobs

• Madrid, Spain
• Hybrid
• €27,200 – €40,800 pa
• Entry level

Acts as the primary point of contact for customers throughout the service and repair journey, managing requests, quotations, orders and escalations. Collaborates with service engineers, repair centres and logistics teams in a regulated MedTech environment, and contributes to process improvements and UAT activities.

Microsoft Office · Outlook · Excel +3

• Edinburgh
• On-site
• £76,800 – £115,200 pa
• Senior

Own the end-to-end data lifecycle for an AI and algorithm R&D team, from clinical study data collection through validation trials. Design and manage scalable infrastructure across clinical trials, sensor platforms and HPC environments, building ETL/ELT pipelines and data tooling in Python and SQL while shaping data architecture standards.

Python · SQL · C++ +3

• 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.

• Oxford
• On-site
• Senior
• Permanent

Hands-on senior role designing, securing and automating Azure cloud infrastructure and CI/CD foundations for regulated medical device software and connected device services. Acts as a bridge between Digital and Data teams, supporting Databricks, SAP interfaces and enterprise data flows, with monitoring, observability and cybersecurity responsibilities. Office-based in Oxford with flexibility.

Azure · Databricks · SAP

• Oxford
• On-site
• Mid-level
• Permanent

Designs mechanical components and assemblies for medical devices using CAD tools, supporting analysis, testing and design verification and validation. Works with manufacturing, suppliers and cross-functional electrical, software and quality teams through the product development lifecycle, preparing documentation to ISO 13485 and participating in risk management and design reviews. Office-based in Oxford with flexibility.

• Darlington
• £65,000 – £85,000 pa
• Director · manages people
• Permanent

Senior leadership role overseeing operations across biologics, RNA and medicines manufacturing facilities at two sites. Leads multidisciplinary teams covering operations, engineering, facilities and site services, ensuring GMP, health & safety and quality compliance while driving continuous improvement, capital projects and operational strategy.

NEBOSH

• Darlington
• £49,045 – £69,045 pa
• Lead
• Permanent

Provide senior scientific and technical leadership across complex RNA manufacturing programmes, informing technical strategy, technology selection and GMP translation. Oversee experimental studies, resolve complex challenges and work cross-functionally with technical, operations, quality, engineering and supply chain teams to deliver scalable, GMP-compatible processes.

• Cambridge
• Remote
• Director · manages people

Leads Jazz's central monitoring capability within Global Clinical Development Operations, defining and interpreting portfolio-level key risk indicators and statistical signals to drive risk-proportionate monitoring strategy at site, study and CRA level. Partners with Trial Risk Management, Site Monitoring, Data Management and Biostatistics, owns RBQM technology platforms, and manages a team of central monitoring analysts.

CTMS · EDC Systems · RBQM Systems +2

• London
• Remote
• Director · manages people

Leads Jazz's central monitoring capability within Global Clinical Development Operations, defining and interpreting portfolio-level key risk indicators and statistical signals to drive risk-proportionate changes in site, study and CRA monitoring strategy. Partners with Trial Risk Management, Data Management and Biostatistics, owns RBQM technology platforms, and manages a team of central monitoring analysts while championing AI-enabled risk detection.

CTMS · EDC

• Raritan, United States
• Hybrid
• US$122,000 – US$211,025 pa
• Lead

Shapes enterprise PLM architecture across MedTech, defining how product data, engineering change control, BOM configuration and lifecycle workflows evolve. Produces blueprints, reference patterns and design principles, guides platform simplification and reuse, and mentors architects while working with R&D, Quality, Regulatory and vendor partners.

Windchill · ThingWorx · Integrity +2

• 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

• Maidenhead
• Hybrid · 3 days in office
• Senior

Executes analytical risk-based monitoring activities across multiple complex clinical trials, reviewing site and subject-level data to detect early risks to data quality, participant safety and compliance. Works closely with Site Managers and Central Monitoring Managers, using data visualisation and reporting tools to guide site prioritisation and engagement.