Latest Regulatory Affairs Specialist Jobs

GDCL International Hubs Director

The Director of International Hubs leads the strategic and operational performance of key international distribution hubs, ensuring service, quality, safety, compliance, and cost efficiency. They work closely with various stakeholders to drive operational excellence and support network transformation initiatives.

Johnson & Johnson MedTech

GDCL International Hubs Director

The Director of International Hubs leads the strategic and operational performance of key international distribution hubs, ensuring exceptional service, quality, safety, and cost performance. They will oversee the Selzach European Distribution Centre and future regional hubs, driving operational excellence and standardization across all locations.

Johnson & Johnson MedTech

Manager Medical Affairs International (m/f/d)

The Manager, Medical Affairs – International is a field-based role supporting the development of professional relationships with key opinion leaders in the therapeutic areas of Shockwave Medical. Responsibilities include providing scientific support, facilitating investigator-initiated studies, and collaborating with cross-functional teams to drive strategic initiatives and ensure compliance with regulations.

Johnson & Johnson MedTech Germany

Manager Medical Affairs International (m/f/d)

This role involves building professional relationships with key opinion leaders in the medical device industry, supporting investigator-initiated studies, and providing scientific expertise for Shockwave Medical products. The Manager will also collaborate with cross-functional teams to develop health economic insights and support internal training.

Johnson & Johnson MedTech

Manager Medical Affairs International (m/f/d)

The Manager, Medical Affairs – International role involves building relationships with key opinion leaders, supporting investigator-initiated studies, and providing scientific expertise for Shockwave Medical products. The position requires extensive experience in medical affairs, particularly in cardiovascular medicine, and strong communication and organizational skills.

Johnson & Johnson MedTech

Experienced I Clin Programmer

Develops and oversees clinical data programming for complex trials, creating CDISC-compliant SDTM datasets and define.xml, implementing data mappings, edit checks, and custom safety/compliance reports. Focuses on data quality, regulatory standards, and integration of diverse clinical data sources to support trial oversight and submissions.

Johnson & Johnson MedTech High Wycombe, United Kingdom

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 monitoring, support inspection readiness, lead quality investigations, and provide strategic guidance on CAPA and regulatory standards within a global, cross-functional R&D environment.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Commercial Quality Senior Specialist Surgery - UK

This role involves leading commercial quality activities for Johnson & Johnson MedTech’s Surgery division in the UK and Ireland, ensuring compliance with medical device regulations and maintaining an effective Quality Management System (QMS). The specialist will manage non-conformances, CAPA investigations, audits, supplier approvals, and change controls while promoting a culture of quality and compliance. The position requires strong regulatory knowledge, collaboration across functions, and experience in highly regulated healthcare environments.

Johnson & Johnson MedTech United Kingdom

Manager Ortho Supply Chain Procurement (SCP)

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

Line Facilitator

The Line Facilitator role involves leading production operations, ensuring compliance with safety, environmental, quality, and business systems. Responsibilities include managing GMP, housekeeping, equipment operation, and non-conformance investigations, while driving operational excellence and maintaining health and safety standards.

Johnson & Johnson MedTech United Kingdom

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

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

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