Director, Regulatory Affairs Jobs in Princeton, NJ

Elevate your career by leading a dynamic regulatory team that shapes promotional strategies for multiple therapeutic franchises, ensuring compliance with FDA regulations and driving impactful business...

Lead the charge in developing regulatory strategies for promotional materials, guiding a team through complex FDA compliance to align commercial goals with regulatory requirements across multiple ther...

Join a dynamic team to lead global regulatory strategy for cutting-edge ophthalmology programs, ensuring alignment with development and commercialization goals while mentoring a high-performing regula...

Champion global regulatory strategies for ophthalmology programs, leading a team to navigate complex challenges in drug development while ensuring compliance and alignment with commercial objectives...

Lead crucial global regulatory strategy in ophthalmology programs while managing a high-performing team. Ensure compliance, drive efficiency, and represent the organization across health authorities t...

Transform regulatory compliance by leading development strategies for diverse products, engaging with agencies, and driving competitive intelligence initiatives within the pharmaceutical landscape...

Innovate regulatory strategies to accelerate product development, ensuring compliance and market readiness through expert guidance and cross-functional collaboration, while managing risks and opportun...

Drive global regulatory strategies for pharmaceutical development programs, ensuring compliance and effective submissions. Lead cross-functional teams and navigate complex regulatory landscapes to ach...

Champion regulatory CMC strategies to elevate cell and gene therapies. Drive cross-functional collaborations, oversee global submissions, and ensure compliance. Lead efforts to mitigate risks and supp...

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...

Drive enterprise Quality and Regulatory governance for U.S. operations, ensuring compliance with FDA regulations and overseeing manufacturing quality in the therapeutic radiopharmaceutical sector whil...

Elevate regulatory content management processes by establishing effective governance, modernization strategies, and digital enablement to enhance efficiency and compliance across global teams and cont...

Join a team that advances global CMC content management capabilities. Lead strategy, enhance processes, and collaborate on digital solutions to modernize regulatory content operations for efficient, c...

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 strategic regulatory CMC initiatives, managing submissions and risk assessments for clinical and commercial products. Collaborate cross-functionally to drive compliance and optimize dossier conte...

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...

Champion the development of regulatory strategies for CMC in gene therapy, facilitating cross-functional collaboration and ensuring compliance while guiding innovative products through clinical to com...

Lead the development and execution of global CMC regulatory strategies to support clinical asset advancement. Collaborate cross-functionally to ensure timely, high-quality submissions and health autho...

Take ownership of CMC regulatory strategies, ensuring compliance and driving product development by collaborating across teams and engaging with regulatory authorities to support key initiatives and s...

Collaborate with cross-functional teams to develop regulatory strategies for CMC. Ensure compliance and drive success for pipeline products by overseeing the preparation and submission of critical reg...

Join a team that drives regulatory excellence for clinical development, ensuring strategic and compliant submissions. Collaborate cross-functionally to accelerate drug approval processes while oversee...

Shape your career by leading the regulatory strategy for critical global products. Collaborate with cross-functional teams to ensure compliance and successful submissions while managing asset developm...

Lead the charge in global CMC regulatory strategies for Cell & Gene Therapy, driving development, registration, and compliance while mentoring managers and guiding submissions aligned with strategic g...

Elevate regulatory standards by coordinating global submissions for medical devices, ensuring compliance with U.S. and international guidelines while supporting cross-functional collaboration and stra...

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...