Director, Regulatory Affairs Jobs in Santa Clara, CA

Lead the global GMP/GDP audit organization, enhancing predictive compliance intelligence while mitigating risks through advanced analytics and effective audit strategies...

Transform the regulatory landscape by leading labeling efforts for animal health products, ensuring compliance and excellence throughout the product lifecycle while collaborating with cross-functional...

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...

Join a dedicated team driving global regulatory strategy for early-stage oncology products. You'll execute and manage high-quality submissions and collaborate across functions to ensure compliance and...

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...

Lead strategic pharmacovigilance initiatives, ensuring compliance and operational excellence for global drug safety, signal management, and regulatory submissions, while preparing for Phase 3 developm...

Oversee global pharmacovigilance initiatives ensuring compliance and safety. Provide strategic leadership in safety surveillance, signal management, and reporting, preparing the organization for regul...

Transform regulatory compliance by supporting submissions and documentation, ensuring adherence to standards, and collaborating with teams to navigate evolving regulations in a dynamic environment...

Play a key role in shaping regulatory strategies for global development programs, ensuring compliance with complex regulatory requirements, and collaborating with cross-functional teams to support mar...

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

Lead the charge in regulatory operations, managing submission strategies and compliance processes. Collaborate across teams to ensure timely, high-quality submissions while optimizing regulatory syste...

Elevate regulatory operations by managing submission strategies and compliance processes. Lead cross-functional teams to ensure timely, high-quality submissions while adapting to evolving regulations...

Lead the charge in regulatory operations, managing submissions and compliance strategies to ensure global regulatory alignment and efficiency across multiple teams and projects...

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...

Elevate the regulatory landscape by guiding strategic promotional communications for Oncology products. Shape impactful messaging while ensuring compliance and aligning with evolving regulations and F...

Drive excellence in quality management by leading electronic systems and compliance initiatives, collaborating across diverse teams to enhance processes and continuously improve quality standards in t...

Unlock potential by leading a global trade compliance program that ensures adherence to international laws while optimizing product flow across the pharmaceutical supply chain. Collaborate with Legal...

Join a team that's driving innovation in R&D and Regulatory processes. Leverage your Veeva RIM expertise, manage global compliance systems, and implement solutions that meet dynamic business needs whi...

Champion regulatory excellence by overseeing compliance and managing the Regulatory Affairs team. Drive strategies for clinical operations while ensuring adherence to FDA guidelines and GCP standards...

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...

Transform the regulatory landscape by leading authoring and management of critical medical writing documents, ensuring clarity and compliance across diverse therapeutic projects from initiation to sub...

Join a team that's redefining operational excellence by leading quality assurance, compliance, and governance initiatives across segments, ensuring standards are met while fostering collaboration and...

Elevate your career by leading GMP Quality initiatives for clinical and commercial products. Oversee external manufacturing operations to ensure compliance, quality assurance, and timely supply while...

Oversee the healthcare compliance program, ensuring adherence to regulations and policies while conducting investigations, training, and audits to mitigate risks and enhance transparency across client...

Unlock potential by leading and executing a comprehensive risk-based Quality audit program, ensuring adherence to GxP regulations and Quality standards. Drive continuous improvement and regulatory rea...