Regulatory Affairs Specialist Jobs in South San Francisco, CA

Optimize regulatory strategies and lead a pioneer team at the forefront of AI-driven drug development, enhancing the delivery of innovative therapeutics across multiple therapeutic areas in a collabor...

Transform global regulatory strategies to meet asset goals and health authority requirements. Collaborate across teams to ensure high-quality submissions and mitigate risks while driving compliance in...

Analyze and drive regulatory CMC strategies for investigational and commercial products, collaborating with cross-functional teams to ensure compliance and success in a dynamic biotech environment. Yo...

Engage customers by leveraging technical sales expertise in scientific instruments. Collaborate with cross-functional teams to meet customer needs and enhance solutions that drive revenue growth and s...

Drive regulatory excellence by leading global strategies for complex surgical robotics and oncology technologies. Collaborate cross-functionally to ensure compliance and optimize market entry while fo...

Pioneer quality assurance in cGMP manufacturing of advanced cell and gene therapies. Ensure compliance with regulations through real-time support, batch reviews, and collaboration with cross-functiona...

Join us as a Technical Specialist to elevate client interactions, lead materials characterization projects, and drive innovative analytical solutions in a collaborative lab setting, transforming techn...

Lead the development and execution of global CMC regulatory strategies, ensuring compliance from discovery through commercialization. Collaborate with cross-functional teams to address regulatory requ...

Manage regulatory submissions and compliance for medical devices. Collaborate across departments to ensure adherence to standards, support audits, and maintain quality throughout clinical processes an...

Lead the charge in compliance strategy for U.S. Commercial and Market Access. Collaborate with senior leaders to guide complex compliance issues, manage risks, and support innovative business objectiv...

Transform supplier quality through rigorous audits and partnerships, ensuring top-notch materials and services meet industry and regulatory standards while driving continuous improvement in the new pr...

Elevate air quality standards through research, regulatory review, and community engagement, leading a team to innovate effective pollution control strategies. Collaborate with stakeholders to create...

Join a team that's shaping healthcare through innovative legal counsel. You'll oversee commercial contracting, guide compliance, and streamline legal operations for critical partnerships in health sys...

Accelerate regulatory strategy development for oncology products, leading global initiatives to secure IND/CTA approvals and marketing applications. Collaborate with cross-functional teams to navigate...

Lead global strategy for Notified Body engagement, ensuring compliance, managing audits, and driving certification readiness across various jurisdictions. Guide integration assessments, enhance proces...

Collaborate with clients and teams to manage projects, expectations, and delivery, ensuring high standards and strategic growth in a fast-paced medical affairs environment. Leverage experience to iden...

Unlock potential by shaping global regulatory strategies for cell therapies, guiding complex programs from development through approval, and driving stakeholder engagement to enhance patient access an...

Join a team that's dedicated to maintaining Good Clinical Practice and human subject protection. Oversee site monitoring, ensure compliance, and support clinical studies through effective communicatio...

Transform regulatory operations by managing and enhancing Regulatory Information Management systems. Drive user adoption, coordinate enhancements, and ensure alignment with business needs in a collabo...

Unlock your potential in clinical safety by reviewing and assessing adverse events in cardiovascular trials. Collaborate with cross-functional teams to ensure compliance and accurate reporting while c...

Lead the charge in establishing and optimizing global regulatory information management strategies. Drive operational excellence while collaborating with cross-functional teams to enhance submissions...

Tackle supplier quality assurance by leading audits, managing compliance, and mitigating risks. Leverage your GMP expertise to enhance Bionova's quality standards and maintain strong supplier relation...

Transform regulatory frameworks for advanced medical devices, guiding teams through compliance and submission processes. Leverage expertise in FDA regulations while fostering cross-functional collabor...

Take ownership of global regulatory and quality strategies for oncology programs. Lead a team to ensure compliance with FDA and global health authorities, supporting rapid execution of early-phase tri...

Manage and enhance the Quality Management System, ensuring all documentation meets GxP requirements and is maintained for inspections. Collaborate cross-functionally to support quality initiatives and...