Senior Regulatory Affairs Specialist Jobs in South San Francisco, CA

Lead the charge in developing and executing global regulatory strategies for innovative therapeutics. Collaborate with cross-functional teams to navigate regulatory pathways and ensure compliance from...

Join a dynamic team to enhance global field action compliance, ensuring regulatory adherence and patient safety. Leverage your expertise in post-market quality to drive continuous improvement and coll...

Join a team that's shaping the future of regulatory affairs by leading cross-functional initiatives in advertising and promotion. Leverage your expertise to drive strategic decisions and enhance commu...

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...

Take ownership of the Quality Management System, ensuring compliance and continuous improvement for medical devices. Collaborate across teams to embed quality throughout the product lifecycle while le...

Lead the charge in regulatory strategy for oncology advertising, guiding cross-functional teams to enhance business initiatives. Utilize industry insights to drive innovation and ensure compliance wit...

Develop and maintain the Quality Management System, ensuring compliance and supporting continuous improvement across quality processes in a regulated environment...

Champion the U.S. Biologics Regulatory CMC team by providing strategic leadership, ensuring timely regulatory submissions, and fostering collaboration among global stakeholders to drive innovative bio...

Transform the CMC regulatory landscape for small molecules, guiding strategies from clinical development to market. Collaborate cross-functionally, author key submissions, and mentor junior staff whil...

Advance quality assurance initiatives by ensuring compliance with cGMPs, overseeing manufacturing operations, and facilitating investigations. Collaborate with teams to maintain high standards in biot...

Drive innovation and transform lives by leading regulatory strategies and submissions for clinical trials globally. Act as a key liaison for project teams to ensure compliance, operational excellence...

Elevate your career by leading global CMC regulatory strategies for biologics. Collaborate with cross-functional teams, ensure compliance, and drive successful product development while mentoring a hi...

Advance regulatory strategies for global CMC submissions, managing cross-functional collaboration and internal processes to meet compliance with health authority standards, while leveraging strong com...

Drive clinical trial success by managing operations, monitoring, and site relationships for diverse studies. Collaborate cross-functionally to ensure compliance, data integrity, and high-quality outco...

Elevate your career by leading CMC Regulatory strategy and execution. Drive submissions, build a high-performing team, and engage with global health authorities to ensure compliance and success in dru...

Empower early clinical development by embedding a proactive quality culture. Serve as a GCP advisor, resolving compliance challenges and enhancing study integrity through strategic partnerships and ri...

Optimize product safety engineering by applying expertise in IEC 62368-1 and IEC 61010-1. Collaborate with teams, mentor junior staff, and manage multiple projects while ensuring compliance with U.S...

Partner with us to innovate and transform Quality & Regulatory operations through technology and data analytics. Drive automation, improve efficiency, and foster effective digital solutions that enhan...

Unlock potential by leading regulatory strategies for innovative medical devices. Collaborate with teams to ensure compliance, execute FDA submissions, manage project timelines, and establish processe...

Elevate our regulatory strategy by providing expert guidance, ensuring compliance, and managing cross-functional partnerships. Lead initiatives that support sustainable growth and adapt to evolving re...

Inspire global product registration strategies while leading cross-functional teams to enhance patient access to diagnostic solutions. Collaborate with stakeholders to ensure compliance and drive inno...

Elevate global regulatory strategies to ensure timely product access and compliance. Collaborate with diverse teams and leaders to embed innovative practices, while guiding a high-performing regulator...

Join us as a Senior Epidemiologist to independently drive real-world evidence initiatives in oncology, focusing on ovarian and lung cancer. Collaborate closely with a dedicated sponsor to enhance earl...

Transform healthcare engagement by building relationships with HCPs through digital interactions and telephone conversations, promoting products, and achieving sales goals while ensuring compliance wi...

Drive supplier quality initiatives by managing audits, compliance evaluations, and corrective actions. Collaborate with suppliers to enhance quality standards and ensure alignment with regulatory requ...