Director, Regulatory Affairs Jobs

Lead regulatory excellence by establishing strategy and governance for multi-facility programs in licensure, compliance, and security while driving sustainable growth and ensuring operational integrit...

Empower regulatory excellence by managing promotional materials compliance across global markets, ensuring adherence to laws and internal policies, while aligning with strategic business objectives in...

Contribute to regulatory leadership in post-approval CMC activities, overseeing global strategies for timely execution of changes in parenteral products. Leverage technical expertise and collaboration...

Champion regulatory compliance and strategy for a highly skilled team while influencing legislative policies through proactive lobbying and industry engagement, driving organizational change and risk...

Lead the charge in driving global regulatory strategy for a vital product portfolio. Collaborate with cross-functional teams to ensure compliance and innovation, shaping strategies that influence busi...

Transform global regulatory strategies for CMC in Cell & Gene Therapy. Lead a team of experts, ensuring compliance with international regulations. Collaborate cross-functionally and drive successful p...

Explore an impactful leadership role managing global CMC RA teams, ensuring compliance and strategic direction for Cell & Gene Therapy products throughout their lifecycle, while fostering collaboratio...

Lead the charge in global CMC regulatory strategy for Cell & Gene Therapy, ensuring compliance across development, registration, and lifecycle management. Oversee regulatory submissions and provide st...

Lead the charge in global CMC regulatory strategies for Cell & Gene Therapy, driving development, registration, and compliance while mentoring managers and guiding submissions aligned with strategic g...

Join us to lead global CMC regulatory strategies for cell and gene therapy products, ensuring compliance with global regulations while supporting the product lifecycle from development to registration...

Lead the charge in shaping regulatory strategy for innovative medical devices. As the key regulatory authority, oversee submissions, compliance, and cross-functional collaboration to drive the success...

Lead the charge in regulatory compliance for promotional and labeling strategies, ensuring alignment with FDA regulations while collaborating with cross-functional teams to achieve business objectives...

Drive the US regulatory strategy for biosimilars, ensuring compliance and facilitating timely approvals through collaboration across functions. Oversee regulatory submissions and lead interactions wit...

Empower medical device compliance by reviewing and submitting regulatory documentation. Collaborate across teams to secure timely approvals while ensuring adherence to FDA, ISO 13485, and global stand...

Lead the charge in establishing and optimizing global regulatory information management strategies. Drive operational excellence while collaborating with cross-functional teams to enhance submissions...

Empower regulatory excellence by leading clinical strategy and submissions. Collaborate with teams to ensure compliance, engage with health authorities, and drive process improvements in a dynamic, fa...

Lead the charge in regulatory strategy development and execution, ensuring compliance for medical devices and pharmaceuticals. Collaborate across teams while advising leadership on regulatory risk and...

Elevate regulatory standards by coordinating global submissions for medical devices, ensuring compliance with U.S. and international guidelines while supporting cross-functional collaboration and stra...

Develop global regulatory strategies to ensure compliance and expedite drug approvals. Lead regulatory submissions, define processes, and guide cross-functional teams throughout the product lifecycle...

Shape the future of Invasive Cardiology as you lead regulatory strategies, manage submissions, and collaborate cross-functionally to ensure compliance and drive innovation in product introduction glob...

Unlock potential by driving global regulatory strategies and quality systems, ensuring compliance and market access for medical devices while guiding cross-functional teams in a collaborative environm...

Join a team that's dedicated to ensuring global regulatory compliance and enhancing quality management. Contribute to medical device approvals and improve processes while gaining ownership of quality...

Unlock global regulatory compliance efforts while enhancing the Quality Management System, leading to market access and continuous improvement initiatives. Collaborate cross-functionally to support re...

Contribute to global regulatory compliance while enhancing the Quality Management System. This role offers growth opportunities for an adept regulatory professional to oversee emerging markets and col...

Shape the future of medical devices by securing 510k and NDA approvals through strategic regulatory compliance. Collaborate cross-departmentally to streamline submissions, maintain documentation, and...