Regulatory Affairs Specialist Jobs in Redwood City, CA

Lead the charge in ensuring continuous regulatory compliance and inspection readiness for R&D technology solutions by executing audit readiness strategies, embedding GxP compliance, and collaborating...

Manage clinical studies to ensure compliance with regulations and human subject protection. Coordinate site monitoring and maintain quality standards while communicating effectively with site teams to...

Join a team that's committed to ensuring compliance and accountability in construction by performing detailed audits of payment applications, guiding project owners, and fostering best practices acros...

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...

Deliver comprehensive supplier quality assessments to ensure compliance with GMP standards. Manage supplier qualifications, client audits, and operational excellence within a dynamic QA team focused o...

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...

Champion regulatory strategy development and implementation for global assets, ensuring compliance and timely submissions while collaborating with diverse teams to minimize risk and drive innovative s...

Join a team that drives GxP project excellence in pharmaceutical manufacturing. Lead initiatives by collaborating cross-functionally to ensure compliance while delivering projects on time and within b...

Join a team that's shaping regulatory strategy in a complex surgical platform. Engage with cross-functional teams to connect product design, clinical workflow, and quality standards, while representin...

Explore opportunities as a Clinical & Regulatory Information Management SME, supporting client delivery across VeevaRIM and Clinical initiatives. Engage with stakeholders, optimize processes, and enha...

Unlock analytical excellence by leading biologic program strategies, driving method development and validation, and ensuring compliance with regulatory standards in a collaborative CMC environment. De...

Join a team that's dedicated to enhancing clinical trial quality through leadership, mentorship, and oversight. Engage remotely with cross-functional teams, driving high standards for patient safety a...

Unlock potential by leading regulatory strategy for clinical gene therapy programs. This execution-focused role drives submissions and health authority interactions while collaborating across cross-fu...

Manage global regulatory strategies for clinical and commercial product registrations. Ensure compliance and successful market access for the PSMA franchise. Lead cross-functional collaborations and d...

Shape quality assurance processes by leading cross-functional initiatives, ensuring compliance with industry standards, and driving continuous improvement for high-quality products and services...

Pioneer regulatory strategies for innovative AI-driven medical solutions. Lead compliance activities and submissions, ensuring adherence to FDA standards while collaborating with cross-functional team...

Transform global CMC regulatory strategies for small molecules and biologics, leading submissions and interactions with health authorities. Oversee a team while ensuring compliance in all development...

Contribute to lead risk-based quality management for oncology trials across phases. Collaborate with cross-functional teams to assess risk, ensure data quality, and drive mitigation. Provide expert gu...

Shape the future of medical information by serving as a key expert in a dynamic role that combines your scientific expertise with technology and content development to ensure high-quality responses fo...

Join a team that's dedicated to enhancing quality across multiple sites, implementing the Quality Management System, and ensuring ISO 9001:2015 compliance while leading strategic audits and process im...

Lead the high-quality monitoring of clinical trials, ensuring compliance with regulatory standards while managing site operations, training staff, and protecting participant safety in a fast-paced, dy...