Senior Regulatory Affairs Specialist Jobs in San Mateo, CA

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...

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...

Drive strategic advisory initiatives in commercial regulatory affairs while leading a high-performing team to navigate complex regulatory landscapes and enhance compliance in pharmaceutical communicat...

Join a team that's dedicated to advancing biopharmaceutical processes. As a Junior CQV Engineer, you'll provide leadership in validation projects, ensuring compliance and quality in commissioning and...

Champion innovative surgical technologies by leading regulatory strategies and shaping clinical evidence. Collaborate with cross-functional teams and senior leaders to navigate complex regulatory path...

Lead the charge in defining and executing the global compliance strategy for clinical development, fostering a quality-centric culture while ensuring adherence to regulatory standards and continuous i...

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

Drive quality excellence in medical devices by leading initiatives, mentoring teams, and ensuring compliance with industry standards. Collaborate across functions to address quality issues and enhance...

Join a team that's driving compliance excellence in supply chain operations. This role blends collaboration across Contracts, Legal, and Supply Chain, focusing on government contracting and ensuring r...

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...

Transform product data management through innovative approaches that ensure accuracy and compliance, while enhancing operational efficiency across diverse enterprise systems. Collaborate with cross-fu...

Join the charge in expanding market presence for Legal Co Counsel, leveraging legal expertise to drive sales and customer solutions. Collaborate with teams to enhance pipelines and deliver AI-driven w...

Partner with us to navigate regulatory landscapes, ensuring compliance and market readiness through specialized rotations in Medical Device Regulatory Affairs while collaborating with industry experts...

Drive your career with an engaging Medical Device Regulatory Affairs role involving hands-on experience through rotations, ensuring compliance and supporting global product releases while collaboratin...

Launch your career in Regulatory Affairs with a dynamic, hands-on program featuring three specialized rotations. Develop compliance skills as you support product registrations and engage directly with...

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...

Manage site operations ensuring efficient flow of information, training, and documentation within clinical research trials while collaborating with multiple departments to enhance trial execution and...

Join our team to empower peptide manufacturing excellence through technical leadership, process optimization, and cross-functional collaboration, driving improvements in yield, efficiency, and complia...

Drive quality initiatives as a key contributor in our Quality Assurance team, ensuring compliance and efficiency in manufacturing and validation processes to uphold the highest quality standards acros...

Lead the charge in Clinical Quality Assurance, ensuring compliance and oversight across clinical studies. Drive team growth, develop audit plans, and support continuous improvement while mentoring jun...

Join a dynamic team to provide executive-level support, manage logistics for meetings, coordinate travel, and facilitate recruitment for a thriving commercialization organization. Your organizational...

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

Join a team that's dedicated to improving healthcare solutions by leading sterilization processes and collaborating with cross-functional experts throughout the product lifecycle, ensuring quality and...

Lead the development of global regulatory strategies and ensure compliance throughout the product lifecycle, from pre-approval to post-approval, as a strategic partner and advisor to cross-functional...