Senior Regulatory Affairs Specialist Jobs in Raritan, NJ

Drive regulatory excellence in product innovation, ensuring compliance and safety while empowering creativity and strategy across teams in a dynamic, collaborative environment. Be the key connector be...

Lead global strategy for Notified Body engagement, ensuring compliance, managing audits, and driving certification readiness across various jurisdictions. Guide integration assessments, enhance proces...

Shape the future of medical devices by leading regulatory CMC strategies, ensuring compliance and collaboration across teams to drive the development of innovative combination products for patients wo...

Champion regulatory excellence by managing eCTD submissions and ensuring compliance with FDA requirements. Collaborate across teams to maintain documentation standards and training while upholding the...

Join a team that's pioneering innovative CMC regulatory strategies for biologics and pharmaceuticals, managing submissions, and providing strategic client support through all stages of drug developmen...

Elevate the regulatory landscape by guiding strategic promotional communications for Oncology products. Shape impactful messaging while ensuring compliance and aligning with evolving regulations and F...

Advance your career by ensuring reliable operations of critical biopharma equipment. Collaborate with teams to troubleshoot, support maintenance, and improve asset reliability in a dynamic, regulatory...

Unlock potential by leading global regulatory strategies in cardiovascular and metabolic programs. Collaborate with cross-functional teams to ensure timely drug approvals while managing complex projec...

Lead the charge in global regulatory strategy development for innovative cardiovascular programs, ensuring efficient approval processes and strategic oversight to accelerate drug advancements through...

Accelerate regulatory strategy development for oncology products, leading global initiatives to secure IND/CTA approvals and marketing applications. Collaborate with cross-functional teams to navigate...

Champion regulatory excellence by leading postmarket strategies for product compliance, driving collaboration across teams to ensure timely submissions and navigate complex regulatory landscapes for c...

Lead sustainability initiatives to optimize energy operations, reducing emissions and costs. Collaborate with maintenance and utility teams to implement energy conservation measures and ensure adheren...

Join a dynamic team to lead global regulatory strategy for cutting-edge ophthalmology programs, ensuring alignment with development and commercialization goals while mentoring a high-performing regula...

Champion global regulatory strategies for ophthalmology programs, leading a team to navigate complex challenges in drug development while ensuring compliance and alignment with commercial objectives...

Transform regulatory strategies for the allergy portfolio, guiding product launches, compliance, and cross-functional collaboration, while mentoring talent and enhancing impact on health and sustainab...

Lead regulatory strategy for advertising, promotion, and labeling compliance across diverse products, ensuring alignment with FDA and global standards while mentoring a talented team. Drive innovation...

Contribute to regulatory excellence by coordinating U.S. submissions, ensuring compliance with FDA standards, and maintaining vital documentation for the Obesity Therapeutic Area, while collaborating...

Unlock your potential by overseeing site management and monitoring for clinical trials, ensuring compliance with regulations and enhancing site relationships to drive quality and timely delivery of cl...

Lead end-to-end GCP audits globally, ensuring compliance and driving improvements in clinical studies. Collaborate with stakeholders to interpret regulations and support regulatory inspections in a dy...

Lead the charge in quality assurance projects, ensuring compliance and timely delivery. Collaborate with cross-functional teams to manage risks, track progress, and drive success through effective com...

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...

Lead the charge in ensuring GMP Quality for investigational programs, collaborating with cross-functional teams and external partners to maintain compliance and oversee lot release for clinical materi...

Join a dynamic team to enhance CCI in packaging and medical devices, driving innovation and method development while providing critical support to late-stage projects and global manufacturing operatio...

Champion regulatory excellence by managing clinical trial submissions, leading a team, and ensuring compliance with government regulations, while collaborating with sponsors and internal departments t...

Shape the future of cell and gene therapy by leading regulatory CMC strategies, overseeing global compliance, and providing expert guidance throughout product development stages. Collaborate with cros...