Regulatory Affairs Specialist Jobs in South San Francisco, CA

Join a team that's dedicated to excellence in Quality Control activities, ensuring compliance and accuracy in complex research submissions. Collaborate with leadership to enhance workflow and drive co...

Lead the charge in navigating complex regulatory challenges for innovative medical devices, ensuring successful approvals in the US and globally through strategic planning and independent judgment on...

Lead the charge in regulatory project management, driving cross-functional execution and strategies for global drug submissions. Collaborate closely with teams to ensure timely completion of critical...

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...

Unlock potential by leading regulatory submissions strategy and excellence across global clinical trials, ensuring compliance and timely approvals while managing risks and aligning with project teams...

Drive quality assurance excellence by overseeing compliance, batch review, and documentation practices, while collaborating with cross-functional teams to enhance operational efficiency and product re...

Champion regulatory excellence in food safety and nutrition, leveraging deep expertise to guide clients through complex compliance challenges and develop impactful strategies for product approvals and...

Champion quality assurance initiatives by leading tests, audits, and compliance efforts. Collaborate cross-functionally to enhance productivity and ensure product integrity while supporting market nee...

Unlock impactful regulatory strategies for global development, driving compliance and excellence in early and late-stage clinical programs while collaborating across teams to facilitate product regist...

Engineer quality solutions in the medical device sector. Oversee compliance, drive risk management, and enhance product quality. Collaborate with teams throughout product lifecycle ensuring adherence...

Pioneer clinical excellence by supporting multiple studies, ensuring compliance with regulations, timelines, and SOPs. Collaborate cross-functionally to generate high-quality clinical evidence while m...

Shape the future of clinical trials by enabling top-notch support and coordination for successful project execution. This role involves interaction with clinical sites, ensuring compliance, and mainta...

Drive regulatory strategy for AI-powered cardiac and pulmonary tools, ensuring compliance and accelerated market access across global markets by leading submissions and fostering cross-functional coll...

Advance your career in regulatory advertising by leading compliance initiatives for promotional materials. Provide strategic guidance across teams, ensuring effective communications that satisfy FDA r...

Elevate client relationships by delivering customized analytical solutions, engaging in dynamic project management, and contributing to innovative materials characterization efforts within a collabora...

Join a team that's committed to excellence in infrastructure projects by developing and managing QA/QC programs to ensure compliance with quality standards, specifications, and regulations across dive...

Join a team that drives strategic CMC regulatory strategies for investigational products, ensuring compliance with global regulations while leading submissions and interactions with Health Authorities...

Lead the charge in bridging satellite technology with global regulatory frameworks, shaping policies, and advocating for spectrum assets, while executing strategic initiatives to enhance worldwide con...

Manage key regulatory functions, guiding compliance in PBM, pharmacy, and healthcare technology. Advise on state and federal obligations, and translate regulations into practical strategies for busine...

Deliver Quality Assurance support in a fast-paced CDMO environment. Collaborate across teams to enhance compliance with GMP regulations and QA systems, ensuring robust quality control processes and co...

Engage in leading GCP audit programs, managing staff development, and implementing quality initiatives to enhance safety compliance. Contribute to a dynamic, science-focused environment dedicated to i...

Shape the future of environmental compliance by leading on-site programs, ensuring adherence to regulatory standards, and fostering sustainability initiatives across operations with minimal supervisio...

Advance your career by ensuring compliance in clinical studies, managing site interactions, and driving quality throughout the research process. Collaborate with teams to support study start-up and mo...

Drive efficiency in project billing and workflow management by overseeing setup, ensuring data integrity, and facilitating vendor invoice processing in Certinia. Collaborate with finance and project t...

Join a team that drives regulatory strategy for companion diagnostics in oncology. Lead cross-functional programs, ensuring successful co-development and alignment of regulatory pathways for both ther...