Senior Regulatory Affairs Specialist Jobs in Bridgewater, 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...

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...

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...

Champion regulatory strategies and submissions for global medical products, ensuring compliance across major markets while leading cross-functional teams and driving process improvements in a collabor...

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...

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...

Lead the charge in regulatory affairs for innovative diagnostics and medical devices. Oversee compliance, manage submissions, and collaborate across teams to ensure successful product market entry and...

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...

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...

Unlock potential by leading regulatory CMC strategies for oncology products, coordinating submissions, and collaborating across teams to ensure compliance and successful product registration in a dyna...

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...

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...

Accelerate your career in Global Regulatory Affairs by supporting drug development programs across multiple therapeutic areas, enhancing your skills in a fast-paced, innovative environment while advan...

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...

Pioneer regulatory excellence by supporting global drug development and lifecycle management across diverse therapeutic areas, while driving collaboration and strategic project execution in a fast-pac...

Shape the future of regulatory strategy by leading projects that ensure compliance and market access. Drive collaboration across teams while managing processes for development and post-approval phases...

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...

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...

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

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...

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...

Lead the charge in ensuring compliance with quality standards through oversight of daily activities, documentation control, and cross-functional collaboration to meet regulatory requirements and drive...

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...

Join our team to lead regulatory strategies across major programs, driving impactful submissions and fostering collaboration within a challenging and dynamic environment. Embrace the opportunity to in...