Director, Regulatory Affairs Jobs

Lead regulatory strategies and maintain compliance with US and international guidelines. Collaborate across teams to manage submissions and foster relationships with regulatory authorities, ensuring a...

Unlock your potential in a dynamic role overseeing regulatory affairs for drug development. Collaborate cross-functionally to shape regulatory strategies and ensure compliance with global guidelines w...

Drive regulatory CMC strategies and submissions for generic drugs, ensuring compliance with FDA regulations. Collaborate with cross-functional teams to facilitate timely approvals throughout the produ...

Lead regulatory strategy and compliance for innovative intraocular devices, ensuring global market access and adherence to safety and quality standards. Drive projects, direct submission strategies, a...

Lead regulatory compliance and strategy for intraocular devices, ensuring timely access to innovative products across global markets while supporting business goals and maintaining high standards of s...

Drive regulatory compliance and strategy for innovative intraocular devices, ensuring timely access across global markets. Collaborate with teams to uphold quality and patient safety in regulatory sub...

Join a team that leads regulatory compliance and strategy for medical devices, ensuring products meet global standards. Drive innovations and support business objectives while maintaining excellence i...

Lead the global regulatory function and drive innovative strategies that propel precision oncology development from early stages to market. Collaborate cross-functionally with teams to navigate comple...

Deliver impactful CMC regulatory support for IND/CTA development and maintenance, ensuring compliance and completeness across submissions while leading cross-functional collaboration and strategically...

Drive regulatory excellence by leading CMC activities for IND/CTA submissions and ensuring compliance across development phases, while collaborating cross-functionally to support innovative oncology p...

Unlock potential by leading CMC regulatory activities for IND/CTA development. Drive compliance and quality in submissions, assess CMC changes, and collaborate cross-functionally to support clinical t...

Oversee innovative regulatory strategies to support transformative clinical programs. Collaborate with cross-functional teams to ensure the preparation of high-quality regulatory submissions while dri...

Transform regulatory strategies to ensure compliance for innovative medical devices while collaborating with cross-functional teams on product development and clinical studies. Drive timely submission...

Transform resource management in Regulatory Affairs by leveraging data to drive strategic workforce planning and enhance operational efficiency across a collaborative environment, ensuring optimal hea...

Lead the regulatory strategy for medical devices, driving submissions and compliance across global markets. Collaborate with R&D and cross-functional teams to manage risks and enhance product lifecycl...

Lead the execution of global regulatory strategies and ensure compliance, acting as a strategic partner across teams. Develop a high-performing regulatory team, simplify processes, and drive operation...

Empower your CMC expertise to drive global regulatory strategy and submissions, ensuring compliance during drug development and commercialization, while collaborating across regions to enhance patient...

Shape the future of regulatory strategy by leading projects that ensure compliance and market access. Drive collaboration across teams while managing processes for development and post-approval phases...

Take ownership of regulatory strategies and submissions for cutting-edge companion diagnostics. Lead a team while interfacing with cross-functional groups and regulatory authorities to navigate the ap...

Join a pivotal role in regulatory affairs, guiding promotional materials in compliance with FDA and provincial guidelines in a dynamic, remote environment. Lead the Materials Review Committee and shap...

Innovate the future of regulatory labeling by driving strategies across global teams, ensuring compliance and quality at all stages of product development while collaborating with key stakeholders to...

Collaborate with cross-functional teams to drive regulatory strategies and manage submissions for drug products. Provide expert guidance to ensure compliance and oversee regulatory activities througho...

Shape the future of pharmaceutical innovation by managing regulatory submissions, supporting product lifecycle, and ensuring compliance with FDA standards for complex generics and combination products...

Join us to drive regulatory strategies for oncology clinical development, collaborating with cross-functional teams. Provide expertise in drug submissions, lead projects, and mentor junior staff while...

Architect strategic CMC regulatory frameworks for biologics development, ensuring compliance from IND through BLA filing while leading cross-functional teams and managing external partnerships within...