Senior Regulatory Affairs Specialist Jobs in Florham Park, NJ

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

Join a team that's driving innovation in R&D and Regulatory processes. Leverage your Veeva RIM expertise, manage global compliance systems, and implement solutions that meet dynamic business needs whi...

Join us to lead global regulatory strategy for innovative development programs, ensuring alignment with business objectives and efficient lifecycle management across major markets while influencing ke...

Drive data excellence by overseeing global regulatory data management activities, ensuring integrity and quality across multiple regions and products. Collaborate with cross-functional teams to innova...

Unlock potential by overseeing global data management activities, ensuring data integrity and quality across regulatory systems. Drive innovation and efficiency through strategic initiatives, while co...

Elevate your career by leading regulatory strategies for US and Canada markets. Drive compliance and innovation for on-market and developing products while collaborating with cross-functional teams to...

Advance your career by leading clinical research projects and ensuring compliance with timelines and standards. Collaborate with stakeholders and clinical sites to safeguard subjects' rights and data...

Elevate patient care by developing global regulatory strategies for innovative medical devices. Collaborate with cross-functional teams to ensure compliance and support product lifecycle management in...

Champion quality assurance excellence in GMP for drug substance and products, overseeing compliance and methodologies. Collaborate to ensure regulatory adherence while maintaining operational efficien...

Empower your career in regulatory affairs through a dynamic fellowship, gaining hands-on experience across diverse therapeutic areas while collaborating with industry leaders to influence drug develop...

Contribute to global drug development by engaging with health authorities, learning regulatory requirements, and tackling real-world projects. This two-year fellowship offers hands-on experience in re...

Champion regulatory excellence by leading CMC strategies for small molecule programs, ensuring compliance and driving successful submissions from early development through commercialization in a dynam...

Lead regulatory operations by overseeing submissions, enhancing processes, and mentoring the team. Ensure compliance and accuracy while managing multiple priorities in a dynamic, remote environment. D...

Join a team that's shaping global regulatory strategy for rare disease therapies. In this pivotal role, you'll lead submissions and agency interactions across the US, EU, UK, and Japan, driving execut...

Lead compliance excellence by conducting quality reviews, enhancing processes, and providing expert guidance to ensure timely, accurate client service and adherence to regulatory standards in a dynami...

Elevate your career by leading regulatory strategy and compliance for diverse product portfolios. Collaborate cross-functionally to ensure successful product launches and ongoing compliance in domesti...

Unlock potential by leading global regulatory strategies for innovative immunology programs. Drive product approval timelines and collaborate with cross-functional teams to ensure compliance and optim...

Unlock your potential by leading cross-functional teams in regulatory affairs, driving strategic initiatives, and leveraging industry knowledge to enhance advertising and promotion practices in the im...

Drive enterprise Quality and Regulatory governance for U.S. operations, ensuring compliance with FDA regulations and overseeing manufacturing quality in the therapeutic radiopharmaceutical sector whil...

Transform your career in regulatory affairs through a dynamic two-year fellowship, gaining hands-on experience across diverse therapeutic areas while collaborating with industry leaders to shape the f...

Champion innovative drug development by engaging in a two-year fellowship, gaining hands-on experience in regulatory affairs, and collaborating with experts to influence health authority strategies an...

Support our Quality Assurance team by ensuring compliance with regulations and company standards through effective release processes, documentation accuracy, and training programs, while collaborating...

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...

Lead cross-functional teams to develop and execute regulatory strategies in oncology advertising and promotion. Drive initiatives, analyze market trends, and enhance communication across departments t...

Champion the U.S. Biologics Regulatory CMC team by providing strategic leadership, ensuring timely regulatory submissions, and fostering collaboration among global stakeholders to drive innovative bio...