Director, Regulatory Affairs Jobs in Oakland, CA

Grow your career with a pivotal role in delivering engaging regulatory education to the insurance sector while building client relationships and collaborating with a dedicated team to ensure complianc...

Engage with cross-functional teams to ensure regulatory compliance for Expanded Access Programs. Drive essential strategies and submissions while staying aligned with global legislation, impacting pat...

Elevate global regulatory strategies as you lead cross-functional teams, ensuring compliance while driving market access for innovative products. Collaborate with stakeholders and health authorities t...

Provide comprehensive Regulatory Affairs support to ensure full compliance with U.S. FDA medical device regulations and international standards, facilitating product submissions and ongoing industry c...

Lead cross-functional collaboration to establish regulatory strategies for drug development, ensuring compliance with ICH guidelines and global health authority requirements throughout product lifecyc...

Lead strategic regulatory consulting efforts for companion diagnostics, integrating insights across IVD development, clinical trials, and commercialization. Collaborate with stakeholders to ensure com...

Unlock compliance potential by leading field strategy for Commercial and Medical teams, ensuring adherence during product launches and expansions while fostering collaboration across stakeholders to s...

Pioneer global regulatory operations by developing strategic initiatives and leading digital transformation efforts. Collaborate with cross-functional teams to enhance compliance and optimize processe...

Transform client relationships by serving as the primary contact for IRB review and advising designated pharmaceutical and academic partners, facilitating timely communications and process improvement...

Transform global regulatory strategy in a leadership role, ensuring effective execution and fostering innovation across Roche’s pharmaceutical portfolio while engaging with top executives and health a...

Advance progress at the forefront of Medical Affairs by managing IME Grants and IST projects. Collaborate cross-functionally to optimize operations, drive process excellence, and support effective med...

Champion operational excellence and strategic partnerships in the clinical research space. Drive financial performance and enhance client satisfaction while leading high-performing teams to achieve su...

Transform regulatory strategies to ensure compliance and facilitate product availability for innovative medical devices in domestic and international markets. Collaborate with teams to navigate comple...

Join a team that's dedicated to supporting regulatory compliance in the medical device industry. You'll collaborate across functions, ensuring timely product registration and maintaining compliance wi...

Transform quality assurance leadership by overseeing CMC QA operations across diverse biopharmaceutical programs, ensuring robust compliance and strategic oversight while fostering a high-performing t...

Unlock potential by leading CMC QA strategy for diverse programs. Guide a high-performing team, ensuring compliance with global regulations while driving quality in biologics, gene therapy, and small...

Lead the development and execution of a global compliance training strategy, enhancing organizational culture through engaging, risk-based programs that meet regulatory standards and industry best pra...

Join a team that's leading the way in Global Patient Safety Operations. Drive strategic oversight for pharmacovigilance operations, managing compliance and quality while developing a high-performing t...

Innovate regulatory processes as a key player in our team, guiding U.S. and international submissions for medical devices. Your expertise will balance compliance and speed, ensuring alignment from con...

Drive global CMC regulatory strategies and submissions for clinical and commercial products. Collaborate cross-functionally to ensure compliance, lifecycle management, and timely delivery of high-qual...

Empower quality excellence by leading complaint management and CAPA programs, ensuring compliance, driving improvement, and fostering collaboration across functions to enhance product safety and effec...

Transform the quality landscape by ensuring compliance and excellence in outsourced GMP manufacturing and clinical operations, driving quality oversight, and fostering a robust quality culture within...

Champion regulatory strategies and submissions for global medical products, ensuring compliance across major markets while leading cross-functional teams and driving process improvements in a collabor...

Innovate global regulatory strategies for complex clinical and CMC submissions. Collaborate with cross-functional teams while mentoring peers. This role requires both independent work and teamwork to...

Join a dynamic team as a strategic leader in global regulatory project management, driving complex submissions and fostering cross-regional collaboration to enhance market access and ensure compliance...