Jobs in Reading

Senior Customer Training Specialist – Hugo RAS Technology

Deliver technical training and clinical education on the Medtronic Hugo RAS robotic surgery system to surgeons and OR staff across Europe. Facilitate hands-on workshops, assess trainee performance, and collaborate with sales, clinical, and medical affairs teams to ensure safe and effective adoption of robotic-assisted surgery in General Surgery, Urology, and Gynaecology. Role involves 75% travel, primarily to a training center in Belgium, with a focus on Portuguese-speaking markets.

Medtronic £58,400 – £87,600 pa

Hybrid Permanent

Senior Clinical Research Specialist

Manages Investigator-Sponsored Research (ISR) studies from initiation to close-out, ensuring compliance with GCP and regulatory standards. Oversees device logistics, financial administration, and contract coordination across global surgical business units. Acts as a European representative on the global ISR Council and leads process improvements in clinical research operations.

Medtronic London, United Kingdom £50,400 – £75,600 pa

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, lead quality investigations, and provide expert guidance to cross-functional teams within a global R&D environment.

Johnson & Johnson MedTech Spain

Hybrid Permanent

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across multiple therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, lead quality investigations, and advise on CAPA plans in a global, cross-functional environment. Key activities include coaching teams, maintaining clinical quality plans, and contributing to governance forums to uphold high standards in clinical development.

Johnson & Johnson MedTech

Hybrid Permanent

Supplier Quality Performance Specialist

This role focuses on enhancing supplier quality performance through data analytics, reporting, and system improvements within a regulated medical device environment. The specialist develops dashboards, identifies quality trends, supports audit readiness, and ensures compliance with international standards like ISO 13485 and 21 CFR 820. Collaboration with cross-functional teams is key to driving continuous improvement in quality systems and governance.

Johnson & Johnson MedTech

On-site Permanent

Supplier Quality Performance Specialist

Manages supplier performance monitoring and quality systems through data analytics, reporting, and compliance oversight. Translates quality data into actionable insights to support decision-making, audit readiness, and continuous improvement across global supply chains. Works cross-functionally with Quality, Compliance, and IT teams to ensure regulatory alignment and system effectiveness.

Johnson & Johnson MedTech US$94,000 – US$151,800 pa

On-site Permanent

Supplier Quality Performance Specialist

This role involves managing supplier quality performance through data analytics, reporting, and system enablement within a regulated medical device environment. The specialist develops dashboards, identifies quality trends, ensures compliance with standards like ISO 13485 and 21 CFR 820, and supports audit readiness by delivering actionable insights. Collaboration with Quality, Compliance, and IT teams is central to improving supplier performance monitoring and governance.

Johnson & Johnson MedTech

On-site Permanent

Supplier Quality Performance Specialist

Monitors and improves supplier quality performance through data analytics, reporting, and system enablement within a regulated medical device environment. Develops dashboards and metrics to support compliance, audit readiness, and continuous improvement across global quality systems. Works cross-functionally with Quality, Compliance, and IT teams to drive data-driven decision-making and enhance quality governance.

Johnson & Johnson MedTech £94,000 – £151,800 pa

Manager, Clinical QA Program Lead

Leads clinical quality assurance audit programs, focusing on GCP compliance across therapeutic areas. Develops and executes audit strategies, supports regulatory inspections, and provides expert guidance on compliance issues. Works closely with cross-functional teams to ensure audit outcomes drive quality improvements and regulatory adherence.

Johnson & Johnson MedTech

Manager, Clinical QA Program Lead

Leads clinical quality assurance audit programs, developing and executing audit strategies across therapeutic areas with a focus on GCP compliance. Conducts and oversees audits, supports regulatory inspections, and drives continuous improvement through data analysis and cross-functional collaboration. Provides expert guidance on compliance issues and contributes to strategic quality initiatives across global clinical operations.

Johnson & Johnson MedTech Switzerland

Hybrid Permanent

Manager, Clinical QA Program Lead

Leads clinical quality assurance audit programs, developing and executing audit strategies across therapeutic areas with a focus on GCP compliance. Conducts and oversees audits, supports regulatory inspections, and drives resolution of compliance issues using data analytics and risk-based approaches. Works closely with cross-functional teams to ensure global alignment of quality standards and continuous improvement in clinical programs.

Johnson & Johnson MedTech

Hybrid Permanent

Manager, Clinical QA Program Lead

Leads and manages clinical quality assurance audit programs across therapeutic areas, focusing on GCP compliance. Develops audit strategies, conducts audits, and supports regulatory inspections. Uses data analytics to identify trends and improve audit effectiveness, while guiding teams and ensuring alignment with global standards.

Johnson & Johnson MedTech

Hybrid Permanent

Manager, Clinical QA Program Lead

Lead and manage clinical quality assurance audit programs, including developing audit strategies, conducting GCP audits, and ensuring compliance across therapeutic areas. Provide expert guidance on regulatory standards, support health authority inspections, and drive resolution of compliance issues. Utilize data analytics to identify trends and enhance audit effectiveness across global operations.

Johnson & Johnson MedTech

Hybrid Permanent