Latest regulatory affairs specialist Jobs

Sr Director, C&SP - NS and Cardio-Pulmonary

The Senior Director, C&SP - Neuroscience & Cardiopulmonary will lead the strategic and operational aspects of Clinical & Statistical Programming. This role involves shaping the long-term vision, guiding organizational evolution, and ensuring flawless execution across major therapeutic and regional portfolios. The position also focuses on building a high-performance organization through talent development and fostering collaboration across various internal stakeholders.

Johnson & Johnson MedTech

Hybrid Permanent

Sr Director, C&SP - NS and Cardio-Pulmonary

The Senior Director, C&SP - Neuroscience & Cardiopulmonary will lead the strategic and operational aspects of Clinical & Statistical Programming. Responsibilities include shaping the long-term vision, guiding organizational evolution, and ensuring flawless execution across major therapeutic and regional portfolios. The role involves leading a large, diverse team, influencing critical portfolio decisions, and championing innovation in clinical evidence delivery.

Johnson & Johnson MedTech

Hybrid Permanent

Product Manager - EMEA

This role involves leading cross-functional teams to develop AI and digital solutions that enhance the orthopaedics supply chain, ensuring timely delivery of medical products. The Product Manager will define product strategy, drive lifecycle management, and deliver data-driven innovations in an Agile environment. The position plays a key part in transforming healthcare through scalable digital technologies.

Johnson & Johnson MedTech €56,400 – €112,800 pa

On-site Permanent

Associate Director, Safety Analysis Scientist

This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages, with responsibility for analyzing complex medical data, supporting global safety strategy, and contributing to regulatory compliance. The scientist will lead safety evaluations, guide cross-functional teams, and ensure high-quality reporting while acting as a subject matter expert during audits and inspections. Innovation in data presentation and process improvement is emphasized within a hybrid work environment.

Johnson & Johnson MedTech Belgium

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

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

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.

Johnson & Johnson MedTech United States

On-site Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for DePuy Synthes, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance in the development of innovative medical devices that improve patient outcomes.

Johnson & Johnson MedTech

On-site Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.

Johnson & Johnson MedTech

On-site Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.

Johnson & Johnson MedTech

On-site Permanent