Latest regulatory affairs Jobs

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

Medical Safety Officer - Solid Tumors

The Medical Safety Officer (MSO) is responsible for assessing the medical safety of Innovative Medicine products and leading cross-functional teams in safety and benefit risk management. Key responsibilities include safety surveillance, risk management, and communication with stakeholders, including Health Authorities and external key opinion leaders.

Johnson & Johnson MedTech High Wycombe, United Kingdom

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)

The Manager Ortho Supply Chain Procurement (SCP) role involves leading procurement activities for the Orthopaedics business, ensuring supplier performance, and aligning procurement strategies with business goals. Key responsibilities include strategic sourcing, supplier management, and driving innovation in new product development.

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

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

Manager Ortho Supply Chain Procurement (SCP)

The Manager Ortho Supply Chain Procurement (SCP) role involves leading procurement activities for the Orthopaedics business, ensuring supplier performance, and aligning with business strategies. Key responsibilities include strategic sourcing, supplier management, and driving innovation in new product development.

Johnson & Johnson MedTech

Senior Process Engineering - Orthopaedics

The Senior Process Engineer is responsible for optimizing manufacturing value streams, leading process development and validation, and driving continuous improvement initiatives. The role involves strategic technical leadership, mentoring junior engineers, and ensuring compliance with quality and regulatory standards.

Johnson & Johnson MedTech United Kingdom