Director, Regulatory Affairs Jobs

Join our team as a regulatory affairs expert, managing global submissions, driving product development, and ensuring compliance with regulatory standards for medical devices to foster innovation and s...

Develop regulatory CMC strategies for global cell therapy products, ensuring compliance with industry standards. Manage submissions, provide guidance to teams, and lead agency interactions to align co...

Join a team that's driving regulatory excellence by supporting compliance and strategy in the Texas competitive energy market, ensuring effective implementation of regulatory requirements and providin...

Join a team that's committed to ensuring compliance with healthcare laws and best practices. You will play a crucial role in guiding the organization through regulatory requirements for pharmaceutical...

Empower global product strategy in Regulatory Affairs, leading teams to navigate complex regulations for therapeutic developments in inflammation and rare diseases. Drive global registration and lifec...

Oversee regulatory review of promotional materials for pharmaceutical products. Ensure compliance with FDA regulations while collaborating cross-functionally to support effective advertising strategie...

Unlock potential by leading regulatory strategies for innovative medical devices. Collaborate with teams to ensure compliance, execute FDA submissions, manage project timelines, and establish processe...

Drive regulatory leadership for early-stage drug development with cross-functional collaboration, supporting strategic business decisions and ensuring strong regulatory alignment throughout product li...

Take ownership of global regulatory strategies for vaccine projects. Oversee regulatory processes, provide expert advice, and lead cross-functional teams to ensure compliance and expedited approvals f...

Shape the future of vaccine development by leading global regulatory strategies, providing expert guidance, and coordinating cross-functional teams. Ensure optimal product approval timelines while uph...

Lead the charge in global regulatory strategy for vaccine and infectious disease projects, ensuring effective oversight, collaboration with cross-functional teams, and engagement with regulatory agenc...

Engage in leading complex regulatory programs across diverse medical devices, ensuring compliance and execution in global markets. Collaborate with cross-functional teams to drive strategic initiative...

Join a team that's shaping the future of drug development by driving innovative regulatory strategies to ensure compliance with global health authority guidelines and supporting the advancement of tra...

Shape the future of regulatory affairs by managing global submissions and compliance for innovative therapeutics, while collaborating with cross-functional teams to support the research and developmen...

Optimize global regulatory submissions and strategies to advance novel therapeutics in Oncology. Collaborate with teams and regulatory agencies to drive compliance and enhance drug development process...

Join a team that's dedicated to regulatory excellence in drug development. As a Manager, you will coordinate global submissions and collaborate with cross-functional teams to ensure compliance and dri...

Elevate regulatory excellence by managing global submissions and interactions. Collaborate across teams to ensure compliance and drive the development of innovative therapies. Play a pivotal role in n...

Unlock your potential by driving regulatory strategy in oncology, ensuring compliance through global submissions and collaboration within cross-functional teams. Contribute to the development of innov...

Grow your career with a dynamic team managing global regulatory submissions, ensuring compliance in drug development. Collaborate with experts to drive innovation in oncology therapeutics, impacting p...

Join a team that's advancing regulatory strategies for innovative oncology therapies. Oversee submissions and compliance, collaborating with cross-functional teams to impact patient care globally. You...

Lead the charge in shaping innovative global regulatory strategies for complex molecules, ensuring efficient clinical pathways and successful health authority interactions throughout product lifecycle...

Unlock potential by leading regulatory CMC submissions and strategies for drug development, ensuring compliance and quality of submissions for small molecules and biologics from inception through post...

Optimize regulatory strategies for advertising and promotion, ensuring compliance with FDA guidance and contributing to cross-functional teams to enhance product messaging and educational materials, w...

Drive growth by leveraging CRO sales experience to cultivate client relationships, enhance market presence, and support strategic initiatives for clinical research solutions across the western United...

Transform regulatory strategies for the allergy portfolio, guiding product launches, compliance, and cross-functional collaboration, while mentoring talent and enhancing impact on health and sustainab...