Latest Quality Engineer Jobs

Product Manager

The Product Manager will join a dynamic AI & Digital team focused on transforming the orthopaedics supply chain with innovative, scalable AI and digital solutions. The role involves strong organizational engagement, cross-functional collaboration, and implementing data-driven solutions to meet the growing demand for personalized care in the medical device industry.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Hips Lifecycle Management Leader - EMEA

The Lifecycle Management Leader for Hips will orchestrate projects across the Hips Value Stream, focusing on innovation and continuous improvement in orthopaedic solutions. This role involves collaborating with cross-functional teams to drive the development and lifecycle management of hip-related medical devices, ensuring they meet clinical and economic standards.

Johnson & Johnson MedTech

On-site 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 drives risk-based oversight, supports inspection readiness, and provides expert guidance on quality issues and corrective actions within a global, cross-functional environment.

Johnson & Johnson MedTech

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role leads clinical risk management across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The Associate Director drives risk-based oversight, inspection readiness, and quality assurance for clinical trials, working closely with global teams to identify, assess, and mitigate risks. They also support audits, develop quality strategies, and provide expert guidance on GCP and regulatory standards.

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

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management activities across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The Associate Director drives risk-based oversight, supports inspection readiness, and advises on quality issues and corrective actions within global clinical trials. They collaborate with cross-functional teams to implement robust quality systems and continuous improvement in clinical development.

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 in Johnson & Johnson's R&D Quality team. The individual will identify, assess, and mitigate quality risks impacting clinical trial data integrity, patient safety, and regulatory compliance. They will drive risk-based oversight, support inspection readiness, lead quality investigations, and provide expert guidance on GCP and regulatory standards across global trial teams.

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 in Johnson & Johnson’s R&D organization, focusing on ensuring data integrity, patient safety, and regulatory compliance in clinical trials. The Associate Director will drive risk-based oversight, support inspection readiness, and provide expert guidance on quality issues and corrective actions. They will collaborate with cross-functional teams to identify, assess, and mitigate risks throughout the trial lifecycle.

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

Hybrid Permanent

Assoc Director, Clinical Risk Management

This role involves leading clinical risk management across multiple therapeutic areas, focusing on ensuring trial data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, and guide cross-functional teams in implementing quality strategies throughout clinical development. A key aspect is providing expert advice on quality issues and leading continuous improvement in clinical trial quality systems.

Johnson & Johnson MedTech Switzerland

Hybrid Permanent

Sr. Manager, Trial Delivery Leader

Leads cross-functional clinical trial teams to deliver global trials on time, on budget, and in compliance with regulatory standards. Oversees end-to-end trial execution, including risk management, budget control, and inspection readiness. Works closely with R&D Quality and regulatory authorities to ensure adherence to global health guidelines and internal processes.

Johnson & Johnson MedTech Spain €75,000 – €129,260 pa

On-site Permanent

Sr. Manager, Trial Delivery Leader

This role leads the operational execution of global clinical trials within Johnson & Johnson MedTech, ensuring trials are delivered on time, within budget, and in compliance with regulations. The Senior Manager oversees cross-functional teams, manages risks, ensures inspection readiness, and drives quality across trial lifecycles. The position plays a key role in advancing innovative medical treatments through structured, patient-focused clinical development.

Johnson & Johnson MedTech France €73,200 – €125,695 pa

On-site 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. Responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and communicating risk updates to stakeholders.

Johnson & Johnson MedTech United States

On-site 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. They actively participate in risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular reviews and governance meetings.

Johnson & Johnson MedTech

On-site 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 active participation in study activities, regular risk reviews, maintaining clinical quality plans, and facilitating risk updates to R&D colleagues.

Johnson & Johnson MedTech

On-site 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. Responsibilities include active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech

On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, collaborates with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include participating in risk assessments, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium

On-site Permanent