Director, Regulatory Affairs Jobs in New Brunswick, NJ

Champion innovative regulatory strategies in a dynamic, global team dedicated to pioneering drug development. Leverage your expertise to navigate complex issues and deliver high-potential therapies ef...

Develop and drive regulatory strategy for clinical-stage programs, ensuring compliance with FDA and international guidelines. Collaborate with cross-functional teams to navigate complex regulatory lan...

Drive global regulatory strategy for medical imaging products, ensuring compliance across the software development lifecycle. Lead a dynamic team, engaging with cross-functional partners and regulator...

Pioneer regulatory excellence by leading global product registrations, ensuring compliance, and guiding teams through complex submissions in the medical device sector for enhanced patient outcomes...

Join a team that's shaping regulatory strategies in biopharmaceuticals. This role involves leading regulatory submissions and collaborating across project teams to ensure compliance while advancing co...

Optimize regulatory strategies by leading a dynamic team to ensure compliance with U.S. standards while collaborating cross-functionally to enhance promotional material oversight and navigate complex...

Empower our regulatory team by leading strategic labeling initiatives and ensuring compliance with FDA regulations for our product portfolio while collaborating cross-functionally to drive successful...

Lead the charge in overseeing complex regulatory projects, ensuring timely and budget-compliant deliverables while managing teams and fostering compliance through innovative solutions and collaboratio...

Join a team that's driving regulatory strategy for a leading product across multiple global markets. Oversee submissions and compliance, ensuring alignment with regulations while collaborating on prod...

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

Empower the development of CMC regulatory strategies for small molecule drugs. Lead global submissions and provide expert recommendations for meeting regulatory requirements, ensuring high-quality com...

Shape strategic regulatory pathways, manage submissions, and liaise with FDA ensuring compliance and efficiency in product development within biotech. Lead projects, advise on regulations, and optimiz...

Pioneer regulatory excellence by leading FDA submissions and compliance. Manage the lifecycle of medical product filings, ensuring alignment with evolving regulations across diverse jurisdictions in a...

Unlock potential by leading regulatory affairs for advertising and promotions. Drive compliance with US and Canadian regulations while guiding cross-functional teams to achieve strategic business obje...

Join a team that's shaping the future of biologics by leading CMC regulatory strategies for new and commercial products, ensuring compliance with global guidelines, and mentoring talented scientists i...

Lead the development of global regulatory CMC strategies for biologics products, ensuring compliance with international regulations. Mentor team members while overseeing complex submissions for succes...

Optimize promotional compliance and strategy by leading regulatory initiatives across brands. Collaborate cross-functionally to ensure effective communication while mitigating risks within a dynamic p...

Lead and transform regulatory strategies for advertising and promotional activities in the US. Collaborate with cross-functional teams to ensure compliance with FDA regulations while supporting innova...

Shape global regulatory CMC strategies for small molecule drug submissions. Lead cross-functional collaboration to ensure timely and compliant documentation for INDs, NDAs, and lifecycle management, w...

Advance your career in regulatory advertising by leading compliance initiatives for promotional materials. Provide strategic guidance across teams, ensuring effective communications that satisfy FDA r...

Join a team that's redefining regulatory CMC strategies for biologics, overseeing the delivery of global submissions while mentoring junior scientists. You’ll ensure compliance and excellence in produ...

Optimize global regulatory strategies for drug programs in cardiovascular metabolic areas. Lead cross-functional teams to secure approvals and navigate regulatory challenges effectively while fosterin...

Unlock potential by leading global regulatory strategies in cardiovascular and metabolic programs. Collaborate with cross-functional teams to ensure timely drug approvals while managing complex projec...

Lead the charge in global regulatory strategy development for innovative cardiovascular programs, ensuring efficient approval processes and strategic oversight to accelerate drug advancements through...

Drive quality excellence and regulatory compliance in a dynamic environment while overseeing quality assurance, control processes, and regulatory submissions to ensure superior product integrity and a...