Regulatory Affairs Manager Jobs in Berkeley Heights, NJ

Unlock your potential by leading regulatory strategies for OTC products. Manage complex projects, enhance stakeholder influence, and develop teams in a fast-paced environment to drive compliance and i...

Join a team that shapes global regulatory strategy in a fast-paced environment. You will lead comprehensive regulatory plans, ensuring alignment and execution from development to post-marketing, impac...

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

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...

Join a team that's redefining regulatory operations, driving strategic compliance and innovation in drug development. Oversee project management, establish regulatory positions, and liaise with agenci...

Engage with cross-functional teams to ensure regulatory compliance for Expanded Access Programs. Drive essential strategies and submissions while staying aligned with global legislation, impacting pat...

Join a team that's dedicated to regulatory excellence, overseeing compliance and submissions while leading cross-functional efforts to align with global standards and foster operational success in a d...

Optimize global regulatory submissions and strategies to advance novel therapeutics in Oncology. Collaborate with teams and regulatory agencies to drive compliance and enhance drug development process...

Elevate regulatory excellence by managing global submissions and interactions. Collaborate across teams to ensure compliance and drive the development of innovative therapies. Play a pivotal role in n...

Unlock your potential by driving regulatory strategy in oncology, ensuring compliance through global submissions and collaboration within cross-functional teams. Contribute to the development of innov...

Grow your career with a dynamic team managing global regulatory submissions, ensuring compliance in drug development. Collaborate with experts to drive innovation in oncology therapeutics, impacting p...

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...

Transform regulatory affairs by leading initiatives that drive innovation and empower cross-functional teams. Shape product strategies, oversee submissions, and collaborate with the FDA to enhance acc...

Engage in global regulatory compliance efforts while enhancing our Quality Management System. This role offers a chance to lead regulatory strategies, influence cross-functional teams, and contribute...

Drive regulatory compliance and quality management for global market access while enhancing your expertise in medical device regulations and expanding your leadership role in this dynamic, cross-funct...

Unlock regulatory leadership in a dynamic biotech setting. Own strategic regulatory initiatives, IND lifecycle management, and represent the organization to the FDA while driving cutting-edge oncology...

Champion regulatory compliance and lifecycle management within non-medicinal product sectors, driving strategies and improving processes for successful product registration, documentation, and market...

Shape the future of pharmaceutical innovation by managing regulatory submissions, supporting product lifecycle, and ensuring compliance with FDA standards for complex generics and combination products...

Unlock potential by leading regulatory submissions and ensuring compliance with FDA guidelines. Collaborate across teams to drive projects efficiently while coordinating with vendors. Your expertise w...

Join a team that drives excellence in regulatory document publishing and management. Oversee the formatting and submission process while ensuring compliance with industry standards, fostering collabor...

Transform regulatory strategies by supporting global submissions in oncology, coordinating agency meetings, and collaborating across teams to ensure compliance and drive clinical development goals. Ma...

Drive the advancement of global regulatory submissions in oncology, ensuring compliance for innovative therapeutics through collaborative interactions and strategic planning in a dynamic, science-focu...

Lead the execution of global regulatory strategies and ensure compliance, acting as a strategic partner across teams. Develop a high-performing regulatory team, simplify processes, and drive operation...

Drive global CMC regulatory strategies and submissions for clinical and commercial products. Collaborate cross-functionally to ensure compliance, lifecycle management, and timely delivery of high-qual...

Engineer innovative CMC regulatory strategies to ensure compliance across product lifecycles. Collaborate with cross-functional teams to deliver high-quality submissions and expert guidance while main...