Director, Regulatory Affairs Jobs in Santa Monica, CA

Take ownership of regulatory strategy and execution to ensure compliance with global health authorities, leading submissions and guiding cross-functional teams in product development activities...

Shape regulatory strategies and lead execution for development programs. Ensure global compliance while overseeing submissions and fostering cross-functional collaboration to achieve regulatory goals...

Champion regulatory excellence for high-risk implantable devices internationally, engaging with global regulators, driving compliance, and leading cross-functional teams to ensure successful market ac...

Join a team that's shaping the future of global regulatory affairs. You will lead compliance strategies for investigational products and marketing applications through effective submissions and collab...

Drive enterprise Quality and Regulatory governance for U.S. operations, ensuring compliance with FDA regulations and overseeing manufacturing quality in the therapeutic radiopharmaceutical sector whil...

Champion compliance excellence by leading regulatory strategies and audits across global operations, ensuring adherence to standards while mitigating risks to enhance patient safety and organizational...

Champion regulatory excellence by guiding project teams, developing global strategies, managing submissions, and ensuring compliance with FDA and international regulations while navigating complex env...

Join a team that drives regulatory excellence for clinical development, ensuring strategic and compliant submissions. Collaborate cross-functionally to accelerate drug approval processes while oversee...

Shape compliance strategies in regulatory affairs, overseeing promotional materials and interactions with FDA. Lead cross-functional reviews, ensuring adherence to guidelines while supporting business...

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...

Join a dynamic team to provide comprehensive regulatory support across clinical, submission, and post-approval phases for pharmaceutical products, ensuring compliance with global regulations while man...

Unlock potential by leading global quality compliance for pharmaceutical products. Drive audit excellence, manage inspection readiness, and partner with teams to ensure adherence to regulations while...

Optimize regulatory strategies and compliance globally by leading cross-functional projects, guiding teams, and liaising with health authorities throughout the drug development lifecycle to ensure suc...

Play a key role in developing and executing regulatory strategies, ensuring compliance for clinical trials and marketing applications, while leading cross-functional teams to manage project timelines...

Shape complex CMC regulatory strategies for innovative cell therapy products, ensuring compliance, timely submissions, and high-quality deliverables while collaborating across diverse teams in a dynam...

Contribute to vital CMC regulatory strategies for cell therapy products, ensuring compliance and quality execution across clinical and commercial phases while collaborating with cross-functional teams...

Lead the charge in driving complex CMC regulatory activities for cell therapy products, enhancing global strategies and ensuring compliant submissions while collaborating with cross-functional teams t...

Shape the future of gene therapy by leading CMC regulatory efforts for cell therapies and lentiviral vectors. Collaborate across teams to ensure compliance, support regulatory submissions, and drive q...

Champion regulatory excellence in CMC for innovative cell therapies, enhancing submission strategies and compliance. Collaborate with cross-functional teams on lentiviral vector processes to drive adv...

Oversee CMC regulatory functions, ensuring compliance for lentiviral vector and cell therapy products. Collaborate with cross-functional teams to support regulatory submissions and strategies, contrib...

Analyze and drive regulatory CMC strategies for investigational and commercial products, collaborating with cross-functional teams to ensure compliance and success in a dynamic biotech environment. Yo...

Manage global regulatory strategies for clinical and commercial product registrations. Ensure compliance and successful market access for the PSMA franchise. Lead cross-functional collaborations and d...

Transform the user experience by leading innovative product strategies, fostering collaboration across teams, and driving the development of impactful solutions that enhance customer satisfaction and...

Unlock potential by leading comprehensive quality assurance programs for supplier management, internal audits, and GMP training. Drive compliance and maintain high standards in a dynamic biopharmaceut...

Lead the development and execution of global CMC regulatory strategies, ensuring compliance from discovery through commercialization. Collaborate with cross-functional teams to address regulatory requ...