Regulatory Affairs Specialist Jobs in New York, NY

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...

Reimagine global compliance strategies as you guide regulatory submissions, assess product impacts, and collaborate across teams to ensure adherence to medical device regulations while enhancing quali...

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...

Drive regulatory excellence by leading pre-/post-market activities for medical devices, developing strategies, performing assessments, and coordinating submissions for successful product lifecycle man...

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...

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...

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...

Drive regulatory excellence by managing submissions, guiding teams, and ensuring compliance. Utilize your expertise to support global projects and foster collaboration in a fast-paced environment focu...

Lead the charge in global regulatory strategies for innovative medical devices, driving project success from registration to compliance. Collaborate across teams to enhance healthcare technologies and...

Drive regulatory affairs strategies globally, enhancing alignment and execution. Collaborate with business units and regional teams to ensure compliance, streamline processes, and foster best practice...

Oversee the management and publishing of regulatory documents, ensuring compliance with Health Authority guidelines. Collaborate with teams on eCTD module coordination while maintaining organized proj...

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...

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...

Manage the creation and publishing of regulatory documents to ensure compliance with Health Authority requirements while coordinating eCTD modules and advising on best practices in document management...

Drive global regulatory strategy execution, ensuring compliance and market access while fostering collaboration across business units and regions, streamlining processes in the medical device industry...

Engage with a dynamic team to facilitate regulatory operations for novel therapeutics. Drive submissions to FDA/CVM while collaborating across multidisciplinary teams to set new regulatory standards i...

Lead the charge in transforming global regulatory strategies into successful outcomes. Oversee regulatory activities and empower teams to ensure quality compliance, timely delivery, and robust cross-f...

Unlock your potential as you drive compliance in FDA regulations, develop product specifications, and collaborate with a dynamic team to ensure accurate labeling and packaging in a fast-paced environm...

Elevate your career in Global Regulatory Affairs by supporting drug development across various therapeutic areas. Join a dynamic team and gain hands-on experience while navigating regulatory challenge...

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

Drive global regulatory labeling initiatives, ensuring compliance and quality of documentation across diverse markets. Lead strategic governance, influence policies, and collaborate cross-functionally...

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...

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...

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...

Join a dedicated team to oversee product quality compliance, manage investigations, and implement corrective actions. Leverage your expertise in regulatory standards to enhance quality systems and dri...