Regulatory Affairs Manager Jobs in Kenilworth, NJ

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...

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...

Drive regulatory strategies and oversee compliance for investigational therapies. Work cross-functionally to ensure timely regulatory filings and maintain vendor relationships, contributing to clinica...

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...

Join a team that's dedicated to ensuring global regulatory compliance and enhancing quality management. Contribute to medical device approvals and improve processes while gaining ownership of quality...

Contribute to global regulatory compliance while enhancing the Quality Management System. This role offers growth opportunities for an adept regulatory professional to oversee emerging markets and col...

Elevate the regulatory landscape by guiding strategic promotional communications for Oncology products. Shape impactful messaging while ensuring compliance and aligning with evolving regulations and F...

Join a team that's dedicated to regulatory compliance and product stewardship, leading efforts across markets in North America. Oversee daily operations, drive continuous improvement, and cultivate a...

Join a dynamic team to drive compliance and regulatory submissions for medical devices in North America, ensuring adherence to FDA and Health Canada standards while collaborating cross-functionally to...

Elevate your career by collaborating with R&D and Regulatory Affairs to implement compliant digital solutions. Utilize your Veeva RIM expertise to enhance global processes and lead technical implement...

Shape compliance strategies and lead regulatory efforts in cosmetics, ensuring adherence to global standards while managing a dedicated team in a dynamic environment. Drive innovation through collabor...

Drive regulatory strategies for advertising and promotions in pharmaceuticals. Conduct independent reviews of promotional materials and ensure compliance while leading product launches and collaborati...

Lead the charge in developing and executing regulatory strategies for advertising and promotional materials. Oversee compliance, manage product launches, and collaborate across teams to maximize compe...

Take ownership of regulatory affairs operations, leading teams to enhance processes within clinical trials while ensuring compliance with regulations and fostering collaboration across departments...

Discover a pivotal role in establishing enterprise data stewardship standards, leading cross-domain collaboration, and ensuring consistency in planning data definitions and accountability across funct...

Transform regulatory landscapes by delivering strategic support for digital health and medical device submissions. Collaborate with teams to ensure compliance and enhance project success through your...

Lead end-to-end GCP audits globally, ensuring compliance and driving improvements in clinical studies. Collaborate with stakeholders to interpret regulations and support regulatory inspections in a dy...

Lead regulatory compliance programs ensuring inspection readiness and proactive risk management across cross-functional teams. Monitor compliance health, manage data quality, and drive improvements al...

Unlock quality excellence in global clinical trials by leading risk-based management strategies. Collaborate across teams to ensure compliance and enhance processes, making a meaningful impact in pati...

Elevate the quality assurance landscape by leading sponsor-side oversight of CMOs through all stages of manufacturing. Drive excellence in compliance, process validation, and regulatory submissions, e...

Unlock growth by serving as a strategic regulatory partner, providing essential guidance for product innovation and market access across multiple stakeholders, ensuring regulatory compliance while dri...

Accelerate progress at the forefront of regulatory affairs, leading CMC strategy and submissions for development and post-approval programs across the EMEA region. Collaborate cross-functionally to en...

Optimize regulatory strategies and compliance globally by leading cross-functional projects, guiding teams, and liaising with health authorities throughout the drug development lifecycle to ensure suc...

Drive operational excellence by managing regulatory affairs processes and supporting scalable promotional material reviews. Collaborate cross-functionally to enhance compliance, training, and automati...