Director, Regulatory Affairs Jobs in Iselin, NJ

Innovate and execute regulatory CMC strategies for radiopharmaceutical products, ensuring compliance across global markets. Collaborate with cross-functional teams to support submissions and enhance p...

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...

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...

Strategize impactful lifecycle regulatory strategies for radiopharmaceuticals, leading a global team to optimize compliance, drive submissions, and ensure seamless cross-functional collaboration while...

Partner with us to lead global regulatory affairs for innovative pharmaceutical products. Oversee strategy, team development, and agency negotiations while ensuring compliance and operational excellen...

Accelerate progress at the forefront of global regulatory affairs by leading strategies for IND/CTA approvals, ensuring product launches, and executing post-marketing initiatives in the oncology secto...

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 your potential by leading global regulatory strategy for groundbreaking genetic medicine products. Drive submissions and interactions with health authorities while mentoring talent in a dynamic...

Drive the US regulatory strategy for biosimilars, ensuring compliance and facilitating timely approvals through collaboration across functions. Oversee regulatory submissions and lead interactions wit...

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...

Empower innovation by leading technology initiatives that enhance regulatory and scientific operations within the medical device sector, ensuring compliance, data integrity, and strategic partnerships...

Elevate your career by spearheading strategic regulatory initiatives in US pharmaceuticals. Leverage your expertise in advertising and promotion to drive impactful solutions while fostering collaborat...

Transform regulatory communication by leading strategy and execution for clear, compliant, and scientifically rigorous documentation. Collaborate with cross-functional teams to support global health a...

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...

Partner with us to drive regulatory strategies and submissions. This role supports cross-functional teams, ensuring quality deliverables and compliance while operating with moderate independence under...

Shape the future of regulatory affairs by driving strategies for late-stage development programs. Collaborate across teams to ensure compliance, manage submissions, and support critical milestones in...

Explore new horizons in regulatory affairs by overseeing CMC strategies, coordinating cross-functional teams, and ensuring compliance with U.S. Health Authority regulations for investigational and mar...

Engage as a Global Regulatory Leader, driving innovative regulatory strategies and interactions to streamline product development and global approval processes, while ensuring compliance and effective...

Take ownership of nonclinical regulatory strategies, steering FDA & EMA interactions and ensuring cross-functional alignment, to facilitate efficient global drug development across preclinical and cli...

Champion global regulatory activities, ensuring high-quality submissions and strategic partnerships. Support lifecycle management across late-stage development, driving compliance with U.S. and intern...

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

Shape the future of regulatory compliance by leading a dynamic team, overseeing U.S. and international filings, and ensuring adherence to industry standards in medical devices. Empower your career whi...

Unlock potential by driving revenue growth in the Pharma & OTC space through strategic sales, client relationship management, and innovative digital solutions. Lead and expand partnerships while ident...

Pioneer the global regulatory strategy for Vaccine & Infectious Disease projects, driving approvals and providing expert guidance throughout the product lifecycle. Lead cross-functional teams and repr...