Regulatory Affairs Manager Jobs in Hackensack, NJ

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...

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...

Unlock potential by managing global regulatory submissions and ensuring timely execution. Collaborate cross-functionally to streamline processes, enhance compliance, and drive project success while co...

Engage in regulatory affairs by leading advertising compliance efforts. You will drive strategy, manage a team, and influence industry standards while ensuring alignment with governmental regulations...

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...

Transform the field of cell therapy by managing critical Sterility Assurance initiatives, supporting facility design, validating aseptic processes, and leading contamination control strategies within...

Lead the charge in developing and overseeing global product labeling strategies for Neuromodulation therapies, ensuring compliance with regulatory standards, and fostering cross-functional collaborati...

Elevate your career by leading global regulatory labeling strategies and initiatives. Oversee labeling governance, ensure compliance, and collaborate with cross-functional teams to support effective p...

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...

Elevate your career as you ensure regulatory compliance in product development and manufacturing. Collaborate with project teams and guide submissions to domestic and international agencies while main...

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...

Join a team that's shaping global regulatory strategies for innovative medical devices. Leverage your expertise in Software as a Medical Device (SaMD) to make impactful submissions and ensure complian...

Engage in leading GCP audit programs, managing staff development, and implementing quality initiatives to enhance safety compliance. Contribute to a dynamic, science-focused environment dedicated to i...

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...

Lead the charge in regulatory strategy, overseeing milestone execution from IND to post-marketing. Collaborate with senior management to guide program teams and ensure excellence in project management...

Lead and empower a team of regulatory compliance experts in supporting a ground-breaking healthcare platform, ensuring regulatory alignment and operational excellence within a complex, evolving enviro...

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...

Empower your career by developing regulatory strategies to ensure timely market access for innovative medical devices. Collaborate with cross-functional teams to guide product development and mitigate...

Join a team that's passionate about advancing regulatory projects in the pharmaceutical industry. Drive compliance and ensure timely submissions while collaborating across functions, developing strate...

Transform the future of healthcare by leading regulatory strategies that accelerate innovative therapies for diverse clients. Join a dynamic team and shape the discourse in biopharma while enjoying fl...

Engage with cross-functional teams to drive regulatory initiatives and compliance in APEJ. Collaborate closely with regulators, contribute to projects, and ensure alignment with HKMA requirements to e...

Empower innovation in quality compliance by overseeing GCP activities, conducting audits, managing regulatory inspections, and ensuring effective risk mitigation strategies throughout clinical develop...

Transform global pharmacovigilance by leading safety assessments, managing risk, and ensuring compliance across clinical trials and regulatory submissions to enhance patient safety and product integri...

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...

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...