Senior Regulatory Affairs Specialist Jobs in San Mateo, CA

Join a dynamic team to provide comprehensive regulatory support across clinical, submission, and post-approval phases for pharmaceutical products, ensuring compliance with global regulations while man...

Unlock potential by guiding regulatory strategies for new and existing medical devices. Collaborate across teams to ensure compliance with global regulations while managing submissions and assessments...

Engage in international regulatory affairs, driving submissions, registrations, and lifecycle management for medical devices in the UK, Japan, and Latin America. Collaborate with regulatory bodies and...

Unlock potential by leading global regulatory submissions and strategic compliance initiatives, ensuring adherence to international standards while mentoring specialists and optimizing project timelin...

Lead regulatory labeling activities to ensure compliance and clarity in product documentation. Collaborate with cross-functional teams while managing external partners, contributing to label design an...

Elevate regulatory processes by coordinating submissions for global approvals, ensuring compliance and facilitating access to vital healthcare technologies through meticulous documentation and project...

Shape the future of regulatory affairs by driving compliance and strategic planning for global product registrations. Collaborate cross-functionally to enhance processes and ensure successful submissi...

Join a team that's dedicated to securing regulatory approvals for innovative medical technologies, ensuring access to life-saving products worldwide while managing multiple submissions and collaborati...

Join a team that's shaping regulatory strategies to drive innovative biopharmaceutical development. Lead submissions, manage agency interactions, and mentor staff while ensuring compliance with evolvi...

Join a team that's committed to driving innovative regulatory projects, ensuring compliance, and collaborating with cross-functional teams to secure timely submissions and approvals for products in th...

Elevate your career by partnering with us in regulatory affairs, where you'll shape global strategies, ensure compliance for medical products, and engage with cross-functional teams to drive success t...

Join a team that's shaping the future of global regulatory affairs. You will lead compliance strategies for investigational products and marketing applications through effective submissions and collab...

Collaborate across functions to design regulatory strategies that ensure compliance, support development programs, and facilitate high-quality submissions. Play a pivotal role in navigating complex re...

Transform the Regulatory Affairs landscape by supporting day-to-day operations, leading initiatives to streamline processes, and ensuring compliance through effective management of submissions and com...

Join a dynamic team as you drive regulatory strategies and ensure compliance in post-approval activities for CMC processes. Collaborate cross-functionally, influencing clinical outcomes and advancing...

Champion global regulatory strategies by leading diverse teams in navigating complex approval processes for medical devices. Drive compliance and ensure optimal product launch pathways while addressin...

Transform regulatory operations by leading submission strategies, managing systems, and ensuring compliance across portfolios while collaborating with cross-functional teams for successful outcomes...

Join a team that's dedicated to ensuring compliance in promotional activities for CNS treatments while navigating regulatory pathways in a fast-paced environment. Help shape communications, drive stra...

Lead regulatory intelligence efforts to ensure compliance and strategic insight within the pharmaceutical landscape. Collaborate across teams to monitor global regulatory changes and support the devel...

Partner with us to drive regulatory compliance excellence in the medical device sector. Support CAPA initiatives, enhance the Quality Management System, and collaborate across teams to ensure adherenc...

Elevate the quality and compliance standards in a dynamic pharmaceutical environment, overseeing validation activities and leading cross-functional teams to ensure regulatory excellence and project su...

Drive regulatory strategies and oversee compliance for investigational therapies. Work cross-functionally to ensure timely regulatory filings and maintain vendor relationships, contributing to clinica...

Empower seamless diagnostic innovation by leading regulatory efforts for new product development. Engage with cross-functional teams to ensure compliance and successful product launches in diverse mar...

Empower regulatory excellence by leading clinical strategy and submissions. Collaborate with teams to ensure compliance, engage with health authorities, and drive process improvements in a dynamic, fa...

Shape the future of medical devices by leading regulatory strategies, ensuring compliance across global markets, and mentoring a dedicated team. Empower innovation through effective communication with...