Director, Regulatory Affairs Jobs in Princeton, NJ

Unlock potential by driving regulatory submissions and managing documentation. Collaborate with global teams to align on strategies, ensuring compliance and effective communication while fostering a c...

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

Lead quality initiatives across contract manufacturers and suppliers, ensuring compliance with global regulations for pharmaceutical and medical device products. Collaborate cross-functionally to driv...

Shape the future of inspection readiness by leading cross-functional initiatives that ensure compliance with global regulations and readiness for audits, while enhancing quality systems and driving co...

Collaborate with cross-functional teams to oversee regulatory activities for a portfolio of Pharmaceutical Diagnostics products, ensuring compliance and strategic alignment with global standards throu...

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

Engineer a risk-based quality strategy ensuring clinical compliance and safety across global operations. Guide audits, inspections, and process optimizations while collaborating with cross-functional...

Take ownership of a comprehensive compliance program, ensuring regulatory readiness and effective oversight across multiple states in telehealth. Lead a team dedicated to establishing policies and fos...

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...

Unlock potential by leading global sterility assurance and contamination control initiatives. Drive compliance and best practices across sterile manufacturing sites while fostering cross-site collabor...

Elevate sterility assurance and contamination control strategies globally. Lead risk assessments and foster best practices across our sterile manufacturing sites while championing continuous improveme...

Transform the biopharmaceutical landscape by advising clients on regulatory compliance and clinical pharmacology strategies, leveraging your expertise to impact innovative drug development across dive...

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...

Join a team dedicated to ensuring drug quality compliance by performing data integrity audits, assessing adherence to FDA standards, and providing actionable recommendations to enhance regulatory deci...

Shape the future of biopharmaceutical development as you lead CMC strategies for antibody and ADC oncology programs, ensuring quality and scalability from early clinical supply to late-stage success...

Manage regulatory submissions and compliance for medical devices. Collaborate across departments to ensure adherence to standards, support audits, and maintain quality throughout clinical processes an...

Manage the preparation and review of regulatory labeling submissions, ensuring compliance with FDA standards while coordinating artwork and drug listings for commercial products and maintaining docume...

Drive growth and customer success by leading consultative sales for CDMO solutions in the pharma sector. Build executive-level relationships and deliver tailored manufacturing support from concept to...

Join us to oversee complex CMC regulatory projects and lead cross-functional teams. Develop strategic direction from global guidelines while ensuring compliance. Represent at key health authority meet...

Provide regulatory expertise by preparing submissions, ensuring compliance, and collaborating with teams to maintain quality guidelines, supporting product development efforts and compliance with glob...

Elevate your career as a strategic leader in global regulatory affairs, managing clinical and commercial drug product compliance. Collaborate cross-functionally to ensure adherence to regulations and...

Make your mark at the forefront of regulatory strategy! Lead clinical and commercial regulatory initiatives, ensuring compliance while driving successful drug product registrations and global submissi...

Provide strategic leadership for quality operations across a global CDMO network, ensuring compliance with GxP regulations and internal standards. Drive quality initiatives, collaborate cross-function...

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...