Senior Regulatory Affairs Specialist Jobs in Irvine, CA

Champion regulatory compliance by supporting quality processes and product lifecycle management in the medical device sector, ensuring adherence to standards during design, development, and commercial...

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

Drive regulatory excellence by shaping compliance strategies for medical robotics. Collaborate across teams to manage submissions, enhance processes, and mentor talent while navigating complex regulat...

Optimize regulatory compliance processes to ensure product quality and adherence to global standards while coordinating submissions and managing cross-functional teams for effective risk management...

Innovate and execute regulatory CMC strategies for radiopharmaceutical products, ensuring compliance across global markets. Collaborate with cross-functional teams to support submissions and enhance p...

Join a team that's shaping regulatory strategies in biopharmaceuticals. This role involves leading regulatory submissions and collaborating across project teams to ensure compliance while advancing co...

Drive compliance by supporting regulatory affairs for medical devices. Collaborate cross-functionally to manage documentation, ensure audit readiness, and maintain quality systems. This hands-on role...

Empower your career by leading regulatory initiatives and guiding teams in compliance with advertising and promotion regulations. Leverage your expertise to influence policies while driving operationa...

Lead the charge in regulatory strategy for clinical studies, providing expert guidance on complex global compliance. Drive communication with health authorities and ensure timely documentation while c...

Play a key role in ensuring regulatory compliance for product development, providing expert guidance on documentation and global regulations to streamline approvals and support product submissions for...

Shape the future of regulatory compliance by leading lifecycle management projects, coordinating approvals, and developing strategies for new medical devices, while fostering relationships with teams...

Lead the charge in regulatory strategy for ophthalmologic products, ensuring compliance with global standards. Manage submissions, coordinate projects, and oversee promotional materials. Join a dedica...

Join a team that's responsible for regulatory submissions and lifecycle management, ensuring compliance with ICH standards. You'll work cross-functionally to identify risks and support global clinical...

Accelerate your career in a dynamic role focused on regulatory CMC submissions, driving compliance and operational excellence in biopharmaceuticals. Collaborate cross-functionally to support both inve...

Join a team that's pioneering transformative cancer immunotherapies. As a key contributor, you will shape regulatory CMC strategies, ensuring compliance and advancing our mission for life-saving treat...

Join a team that's transforming healthcare by preparing regulatory submissions for complex biopharmaceutical products while ensuring compliance with global standards and driving improvements in Regula...

Join a dynamic team and lead regulatory strategies for in vitro diagnostics, ensuring compliance and successful submissions while collaborating cross-functionally. Manage project timelines and mentor...

Lead critical clinical strategies and ensure regulatory compliance while collaborating across teams to uphold data integrity and support product development initiatives in a dynamic environment...

Drive regulatory compliance for product development and manufacturing, ensuring alignment with global requirements. Oversee documentation for submissions and monitor regulatory changes impacting proje...

Champion the development of CMC regulatory submissions and strategies, ensuring compliance with global standards. Collaborate with cross-functional teams while maintaining accuracy in documentation to...

Lead the charge in managing CMC regulatory submissions and strategies, collaborating with cross-functional teams to ensure compliance and support the lifecycle of innovative therapies within a dynamic...

Empower your career by supporting critical CMC regulatory activities. Collaborate with cross-functional teams to ensure compliance and contribute to successful global submissions in an innovative biop...

Transform clinical trial management by maintaining essential documents and trackers, ensuring compliance with regulations, and supporting study teams throughout trial phases. Contribute to efficient o...

Support regulatory compliance and enhance quality assurance processes across global medical device markets. Collaborate with cross-functional teams to maintain quality standards and drive continuous i...

Transform the future of healthcare by leading regulatory strategies that accelerate innovative therapies for diverse clients. Join a dynamic team and shape the discourse in biopharma while enjoying fl...