Latest Quality Engineer Jobs

Hips Lifecycle Management Leader

The Hips Lifecycle Management Leader role involves leading the lifecycle management of hip orthopaedic products, driving innovation and ensuring the delivery of high-quality, less invasive, and personalized treatments. The role is part of a global team focused on advancing orthopaedic solutions and improving patient outcomes.

Johnson & Johnson MedTech United States

On-site Permanent

Hips Lifecycle Management Leader

The Hips Lifecycle Management Leader role involves leading the lifecycle management of hip joint products within the MedTech Orthopaedics business. Responsibilities include strategic planning, product development, and ensuring the delivery of innovative and personalized treatments. The role is part of a global team focused on advancing orthopaedic solutions and improving patient outcomes.

Johnson & Johnson MedTech

On-site Permanent

Experienced I Stat Programmer

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...

Johnson & Johnson MedTech High Wycombe, United Kingdom

Senior I Stat Prog Lead

This role involves leading statistical programming activities for clinical projects, developing programming strategies, and delivering high-quality data analysis and reporting. The Senior Statistical Programming Lead provides technical guidance to teams, ensures compliance with data standards and SOPs, and contributes to submissions and cross-functional initiatives. It emphasizes advanced SAS programming, clinical trial data structures, and collaboration within a regulated environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Experienced I Clin Programmer

This role involves leading clinical programming activities for MedTech trials, focusing on data modeling, CDISC SDTM submissions, and developing reporting solutions for safety and compliance monitoring. The programmer will create and review specifications, implement data transformations, and ensure adherence to regulatory standards. Work includes both internal data review models and submission-ready deliverables.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across complex trials and programs, ensuring data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, and advise on quality issues and corrective actions in a global, cross-functional environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Lead Local Trial Manager

The Lead Local Trial Manager is responsible for managing and overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, maintaining high-quality data, and collaborating with internal and external stakeholders to deliver successful trials.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Senior Local Trial Manager

The Senior Local Trial Manager is responsible for overseeing clinical trials in the UK, ensuring compliance with protocols, SOPs, and regulatory standards. Key responsibilities include coordinating trial activities, managing site selection, and maintaining relationships with external and internal stakeholders. The role involves process improvement, mentoring team members, and delivering high-quality data.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and facilitating regular risk updates to R&D colleagues.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Medical Advisor/Sr. Medical Advisor

This role involves providing high-quality medical input and leadership in oncology, collaborating with cross-functional teams to drive medical strategy and patient outcomes. Responsibilities include building expertise in oncology, gathering field insights, and contributing to evidence generation and medical affairs projects.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Sr Director, External Scientific Innovation Transactions

The Sr Director, External Scientific Innovation Transactions leads business development activities, including transactions, research collaborations, licensing, and asset acquisitions. They focus on identifying and securing top scientific innovations, primarily in the APAC region, and work closely with R&D, finance, legal, and IP teams to develop and execute complex deals.

Johnson & Johnson MedTech London, United Kingdom

On-site Permanent

Lead Product Analyst, IM SCT Deliver – Customer Order Experience

The Lead Product Analyst will manage IT solutions for customer order experiences, collaborating with business and technology teams to deliver user-centric, industry-leading strategies. Key responsibilities include driving integration with commercial and supply chain systems, evaluating industry capabilities, and fostering a culture of innovation and talent development.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

D&A and Master Data Specialist

This role focuses on maintaining master data integrity across commercial systems, ensuring data accuracy, compliance, and consistency. The specialist will implement data governance practices, support MDM system implementations, and collaborate with cross-functional teams to improve data processes. Using tools like Power BI and Excel, they will generate insights and support data quality initiatives across regions.

Johnson & Johnson MedTech Germany €62,500 – €97,865 pa

Hybrid Permanent

Content Compliance Specialist

This role involves managing and improving content compliance and copy review processes across EMEA markets for MedTech promotional materials. The specialist ensures regulatory adherence, supports audit readiness, and drives process efficiency through digital tools, AI, and automation. They provide guidance to submitters, maintain documentation, and contribute to system enhancements in a multilingual, cross-regional environment.

Johnson & Johnson MedTech €67,500 – €106,835 pa

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 position supports inspection readiness, drives risk-based oversight, and collaborates with cross-functional teams to implement effective quality strategies and corrective actions.

Johnson & Johnson MedTech Spain

Hybrid Permanent