Jobs in Reading

Senior Clinical Research Specialist

Manages Investigator-Sponsored Research (ISR) studies from initiation to close-out, ensuring compliance with GCP and regulatory standards. Supports clinical documentation, financial administration, and device logistics across global Surgical business units. Acts as a European representative on the global ISR Council and leads process improvements in contracting, payments, and compliance workflows.

Medtronic £50,400 – £75,600 pa

Associate Dir. Cross TA Risk Management

This role leads clinical risk management across therapeutic areas in J&J's R&D organization, focusing on ensuring data integrity, patient safety, and regulatory compliance in clinical trials. The individual will drive risk-based oversight, support inspection readiness, and provide expert guidance on quality issues and CAPA plans. The position operates in a global, cross-functional environment and contributes to shaping quality systems and processes across clinical development.

Johnson & Johnson MedTech United States US$122,000 – US$212,750 pa

Hybrid Permanent

Sr. PM, Network Transformation

Leads the planning and execution of complex supply chain network transition projects within Johnson & Johnson MedTech’s EMEA Distribution Network Strategy. Coordinates cross-functional initiatives including site cutovers, operational readiness, and stakeholder alignment to deliver a future-state asset-light distribution model. Focuses on governance, risk management, and disciplined project delivery across multiple interdependent workstreams.

Johnson & Johnson MedTech

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring data integrity, patient safety, and regulatory compliance in global clinical trials. The Associate Director drives risk-based oversight, inspection readiness, and quality governance, working closely with cross-functional teams to identify, assess, and mitigate risks throughout trial lifecycles. They also support audits, inspections, and the development of corrective actions, contributing to a robust quality framework in R&D.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring data integrity, patient safety, and regulatory compliance in global clinical trials. The Associate Director will drive risk-based oversight, inspection readiness, and quality investigations, while advising trial teams and collaborating with cross-functional stakeholders to maintain high standards in clinical research quality.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, develop Clinical Quality Plans, support inspection readiness, and advise on quality issues and CAPAs in a global, cross-functional environment.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent

Assoc Director, Clinical Risk Management

This role involves leading clinical risk management activities 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 monitoring, support inspection readiness, lead quality investigations, and provide expert guidance on GCP, CAPA, and regulatory standards within a global, cross-functional R&D environment.

Johnson & Johnson MedTech Switzerland

Hybrid Permanent

Senior Development Engineer|Johnson & Johnson MedTech| Orthopaedics| R&D

Lead and contribute to orthopaedic medical device development from concept through to launch, applying design controls, risk management, and verification testing. Collaborate with cross-functional teams including design, quality, manufacturing, and regulatory to deliver safe, effective, and compliant solutions. Support documentation, mentor junior engineers, and drive innovation in joint reconstruction technologies.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Senior Development Engineer| J&J| R&D

Lead and contribute to the full product development lifecycle for orthopaedic medical devices, from concept to launch, ensuring compliance with design controls and regulatory standards. Collaborate with cross-functional teams including design, manufacturing, and quality to develop innovative joint reconstruction solutions. Support technical problem-solving, prototype testing, and design transfer while mentoring junior engineers and driving continuous improvement in R&D processes.

Johnson & Johnson MedTech United States

Supplier Quality Performance Specialist

This role involves using advanced data analytics to monitor and improve supplier quality performance within a regulated medical devices environment. The specialist develops dashboards and reports to track quality metrics, supports audit readiness, and collaborates with cross-functional teams to ensure compliance with regulatory standards. The position focuses on translating complex quality data into actionable insights to strengthen governance and drive continuous improvement in supplier quality systems.

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

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 GCP audits, supports regulatory inspections, and drives resolution of compliance issues through data analysis and cross-functional collaboration. Provides expert guidance on quality and regulatory matters while managing complex audit projects and mentoring auditors.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Lead MSA SOP Strategy & External Envir

This role leads the strategy and governance of Standard Operating Procedures (SOPs) for Medical and Scientific Affairs (MSA) within DePuy Synthes, focusing on clinical research, medical affairs, and evidence generation for orthopedic medical devices. The position ensures global regulatory compliance, drives SOP updates in response to evolving standards, and coordinates cross-functionally to maintain audit readiness. It plays a key role in aligning clinical evidence processes with regulatory intelligence and operational excellence in a highly regulated MedTech environment.

Johnson & Johnson MedTech Leeds, United Kingdom

Hybrid Permanent

Supplier Quality Performance Specialist

This role involves managing supplier quality performance through data analytics, reporting, and system enablement within a regulated medical devices environment. The specialist develops dashboards, identifies quality trends, supports audit readiness, and ensures compliance with QMS standards such as ISO 13485 and 21 CFR 820. Collaboration with Quality, Compliance, and IT teams is central to driving continuous improvement in supplier quality systems.

Johnson & Johnson MedTech

Supplier Quality Performance Specialist

This role focuses on enhancing supplier quality performance through data analytics and reporting within a regulated medical device environment. The specialist develops dashboards, identifies quality trends, supports audit readiness, and ensures compliance with regulatory standards like ISO 13485 and 21 CFR 820. Collaboration with Quality, Compliance, and IT teams is central to driving continuous improvement in quality systems and supplier performance monitoring.

Johnson & Johnson MedTech United States

On-site Permanent

Supplier Quality Performance Specialist

This role focuses on supplier quality performance by developing and maintaining quality metrics dashboards, analyzing compliance data, and supporting audit readiness. The specialist works cross-functionally with Quality, Compliance, and IT teams to ensure data integrity and drive continuous improvement in quality systems. It involves translating complex quality data into actionable insights to strengthen governance and regulatory compliance across the organization.

Johnson & Johnson MedTech

On-site Permanent