Director, Regulatory Affairs Jobs in Florham Park, NJ

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

Shape the future of patient care by leading global regulatory strategies for clinical trials, ensuring compliance and efficient execution across multiple regions throughout the product development lif...

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...

Lead the future of pharmacovigilance as a domain expert, shaping innovative systems and processes to enhance patient safety through AI-enabled solutions and cross-functional collaboration in complianc...

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...

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

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...

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...

Accelerate progress at the forefront of regulatory affairs, leading CMC strategy and submissions for development and post-approval programs across the EMEA region. Collaborate cross-functionally to en...

Empower the Regulatory Affairs team by driving compliance and strategy across global projects. Lead regulatory submissions, monitor changes, and collaborate with stakeholders to ensure successful prod...

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...

Explore the intersection of innovation and compliance as a leader driving regulatory strategies across the Americas, ensuring product safety and adherence to key legislation while supporting groundbre...

Join a team that's committed to upholding compliance and quality standards within US commercial operations, overseeing critical quality activities, and driving continuous improvement initiatives to en...

Empower a dynamic compliance culture by leading policy development, training, and third-party due diligence initiatives. Collaborate cross-functionally to enhance compliance governance and support cor...