Senior Regulatory Affairs Specialist Jobs in Mahwah, 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...

Elevate regulatory standards by coordinating global submissions for medical devices, ensuring compliance with U.S. and international guidelines while supporting cross-functional collaboration and stra...

Lead the charge in optimizing global regulatory affairs by supporting critical business operations and enhancing user experience through effective documentation, training, and change management, ensur...

Transform the regulatory landscape by leading product lifecycle strategies, ensuring compliance in global markets, and collaborating with multidisciplinary teams for medical device advancements...

Strategize regulatory affairs initiatives to guide product lifecycle management, ensuring compliance across U.S. and international markets while collaborating with cross-functional teams and regulator...

Join a team that's committed to ensuring compliance with regulatory standards by managing product development and labeling processes. Collaborate with cross-functional teams to navigate regulatory lan...

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...

Champion data-driven decision-making by analyzing complex datasets and translating insights for market access strategies. Collaborate cross-functionally to drive operational efficiency and support reg...

Join our dynamic team to drive regulatory compliance, support product safety initiatives, and collaborate across functions to ensure adherence to global regulations. Your expertise will be crucial in...

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 revolutionizing surgical solutions by driving regulatory strategy and approval processes for cutting-edge medical devices. Collaborate with engineering and clinical teams to bring i...

Join our innovative team to lead regulatory strategies for robotic surgical instruments. Collaborate closely with engineering and clinical teams to drive product development and ensure timely global r...

Join a team that's shaping the future of global regulatory affairs. You will lead compliance strategies for investigational products and marketing applications through effective submissions and collab...

Transform quality assurance processes by managing third-party compliance and leading cross-functional initiatives for product lifecycle success while driving continuous improvement at external manufac...

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...

Join a dynamic team as you drive regulatory strategies and ensure compliance in post-approval activities for CMC processes. Collaborate cross-functionally, influencing clinical outcomes and advancing...

Champion global regulatory strategies by leading diverse teams in navigating complex approval processes for medical devices. Drive compliance and ensure optimal product launch pathways while addressin...

Join a team that's dedicated to ensuring compliance in promotional activities for CNS treatments while navigating regulatory pathways in a fast-paced environment. Help shape communications, drive stra...

Redefine regulatory excellence by leading critical initiatives in diagnostics and clinical lab settings. Collaborate with cross-functional teams to ensure compliance and effectiveness in product regis...

Champion regulatory initiatives for in vitro diagnostics, guiding submissions and strategy globally. Foster cross-functional collaboration to drive compliance and product approval while enhancing safe...

Lead the charge in enhancing global quality through regulatory intelligence and external engagement. Drive strategy, monitor trends, and ensure compliance while collaborating with stakeholders to advo...

Optimize global quality processes by leading regulatory intelligence, advocacy, and engagement. Ensure timely communication of regulatory changes and alignment with key stakeholders to drive complianc...

Advance regulatory compliance as a key member of a collaborative team, ensuring timely solutions for product registration and commercialization. Solve complex challenges and foster innovation while sa...

Lead the charge in optimizing clinical trial operations, ensuring compliance and data integrity across multiple sites. Collaborate with investigators and cross-functional teams to enhance trial qualit...