Regulatory Affairs Manager Jobs in San Jose, CA

Lead our regulatory operations team in navigating UDI compliance and FDA regulations for medical devices, ensuring accurate registrations and supporting cross-functional initiatives that enhance produ...

Join a team that's dedicated to advancing regulatory strategies for complex diagnostics. Collaborate cross-functionally to ensure compliance and optimize product access, while influencing global regis...

Pioneer innovative regulatory strategies for complex IVD projects while ensuring compliance with global regulations. Collaborate cross-functionally to enhance stakeholder relationships and drive timel...

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...

Champion compliance and innovation by advising cross-functional teams on FDA advertising regulations, driving strategic decisions to mitigate risks while supporting business objectives in healthcare c...

Elevate the field of diabetes care by developing comprehensive global regulatory strategies, ensuring compliance while leading a dynamic team to innovate solutions that enhance patient lives and healt...

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...

Transform regional regulatory engagement by leading strategy, fostering relationships, and advocating for efficient electric transmission policies. Collaborate across departments to align regulatory g...

Transform global regulatory submission strategies and ensure compliance with health authorities while collaborating across teams for better patient outcomes. Leverage your expertise to navigate comple...

Lead the charge in ensuring compliance and operational excellence in regulatory affairs, supporting product registrations and inter-department collaboration. Drive impactful strategies for diabetes ca...

Shape the future of regulatory strategy by leading projects that ensure compliance and market access. Drive collaboration across teams while managing processes for development and post-approval phases...

Contribute to regulatory excellence by leading teams to develop successful strategies for biotech and pharmaceutical projects, ensuring compliance with FDA and global agencies while enhancing innovati...

Shape regulatory strategy and drive excellence for innovative diabetes care products while leading a talented team and collaborating cross-functionally. Ensure compliance and timely submissions to bri...

Shape the future of diabetes management by leading regulatory strategies, mentoring a team, and ensuring compliance excellence to launch innovative products that enhance patient lives and streamline m...

Shape global regulatory operations by leading submission strategies, establishing best practices, and managing high-performing teams to ensure timely, compliant, and inspection-ready submissions acros...

Drive regulatory compliance and product approval processes for innovative medical devices. Collaborate across teams to develop strategies and submissions, ensuring adherence to global regulations whil...

Take ownership of U.S. regulatory submissions, ensuring accuracy and compliance with FDA requirements. Collaborate cross-functionally to coordinate IND, NDA, and BLA filings, executing processes withi...

Lead the charge in regulatory affairs as a pivotal contributor, shaping strategies and managing complex submissions across global oncology programs while collaborating cross-functionally to ensure com...

Optimize regulatory operations by coordinating submissions, ensuring compliance, and collaborating with cross-functional teams. You'll empower the Regulatory Affairs department through effective commu...

Champion the global regulatory strategy for complex CGT products, driving approval pathways and guiding cross-functional teams. Leverage your expertise in oncology and cell therapy to influence stakeh...

Champion global regulatory activities, ensuring high-quality submissions and strategic partnerships. Support lifecycle management across late-stage development, driving compliance with U.S. and intern...

Champion global regulatory strategies for medical devices, ensuring compliance from development through market approval. Collaborate cross-functionally to assess compliance and support international e...

Collaborate to lead regulatory projects, ensuring compliance with state and federal standards while enhancing internal processes and fostering strong stakeholder relationships for timely project compl...

Lead CQV activities for pharmaceutical projects, ensuring compliance with FDA regulations. You will manage teams while overseeing project schedules, budgets, and collaboration across functions to supp...

Join a team that's leading commissioning, qualification, and validation for pharmaceutical manufacturing projects. You will manage cross-functional teams, ensure compliance, and drive project success...