Regulatory Affairs Manager Jobs in Wayne, NJ

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...

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...

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...

Elevate your career by leading innovative Regulatory Affairs projects that drive excellence across teams. This strategic role involves optimizing processes, ensuring compliance, and managing complex p...

Champion regulatory strategies and submissions for global medical products, ensuring compliance across major markets while leading cross-functional teams and driving process improvements in a collabor...

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...

Provide comprehensive Regulatory Affairs support to ensure full compliance with U.S. FDA medical device regulations and international standards, facilitating product submissions and ongoing industry c...

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...

Transform relationships into growth by managing a diverse portfolio of global ecommerce merchants. Build strategic partnerships, optimize client experiences, and drive revenue through collaboration an...

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...

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...

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...

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 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...

Champion global CMC regulatory strategies, ensuring compliance and facilitating timely market entry for OTC and nutraceutical products while collaborating across teams to drive innovation and quality...

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 U.S. regulatory strategies in Obesity and Related Conditions, ensuring compliance and patient safety. Lead teams on global initiatives and manage key submissions for clinical trials and mark...

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...

Manage site-level regulatory operations for clinical trials, ensuring compliance with U.S. regulations. Collaborate with cross-functional teams and provide guidance for regulatory submissions, fosteri...

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...