Senior Regulatory Affairs Specialist Jobs in Princeton, NJ

Elevate the quality oversight for GMP activities by managing third-party vendors, leading investigations, and ensuring compliance in the clinical supply chain. Collaborate cross-functionally to drive...

Support quality oversight in clinical supply chain management, enhancing compliance and collaboration with external contractors. Lead investigations, manage vendor relationships, and drive strategic i...

Explore opportunities to enhance quality oversight in clinical supply production, driving best practices and compliance in collaboration with external contractors while leading critical quality projec...

Lead the charge in analytical method validation and cGMP activities, ensuring compliance and quality in support of clinical and commercial development of small molecules and investigational products...

Lead the charge in shaping the Supply Chain Intelligence portfolio. You'll collaborate across teams to transform data into impactful product solutions, driving customer satisfaction and business value...

Elevate product development by leading end-to-end feature delivery, collaborating across teams to transform ideas into impactful solutions for users, and enhancing care delivery through innovative tec...

Join our team as a Regulatory Senior Specialist, managing regulatory tasks for OTC drug and cosmetic projects across multiple business units while collaborating with cross-functional partners to drive...

Empower clients to master supply chain risk analysis while ensuring compliance in complex regulatory environments. Collaborate with customers to uncover insights and drive engagement through expert pr...

Champion operational excellence by leading and mentoring the Global Pharmacovigilance team to ensure compliance and quality in safety practices, while driving process improvements and team development...

Take ownership of quality control processes in an analytical lab, ensuring compliance with industry standards while supporting method validation and training team members for success in pharmaceutical...

Oversee preclinical operations by managing non-GLP and GLP toxicology studies, ensuring scientific and corporate goals are achieved while complying with regulatory standards and fostering collaboratio...

Drive compliance and reliability in the electric utility sector, ensuring adherence to NERC Operations & Planning and CIP standards to enhance grid stability and security. Collaborate with teams to im...

Lead the charge in establishing and managing a new QC Microbiology lab, ensuring compliance with FDA regulations and efficient operations to support GMP manufacturing and testing of materials, interme...

Drive operational excellence in multi-country medical device clinical trials, overseeing planning, execution, and vendor management throughout the European Union, ensuring compliance with regulations...

Elevate your career as a Senior Import/Export Specialist driving compliant and efficient global trade operations. Lead analytics, process design, and cross-functional initiatives, ensuring compliance...

Pioneer clinical research in Oncology, driving innovative strategies and managing trials from inception through analysis, ensuring efficacy and safety for investigational drugs while collaborating acr...

Drive your career forward by leading clinical research for innovative Oncology medicines, overseeing study design, execution, and regulatory processes while collaborating with cross-functional teams t...

Oversee and drive the strategic direction of global clinical trials, ensuring regulatory compliance and operational excellence from initiation to completion while leading cross-functional teams to del...

Lead the charge in advancing innovative oncology research by ensuring exemplary site operations and compliance, fostering strong collaborations, and enhancing recruitment strategies to meet project ob...

Transform manufacturing processes for medical devices. Collaborate cross-functionally to enhance compliance, efficiency, and sustainability while executing validations and driving continuous improveme...

Advance enterprise data quality practices that ensure accuracy and reliability of vital data assets, driving improvements across multiple teams to support analytics, innovation, and regulatory excelle...

Lead the charge in establishing enterprise-wide data quality standards and practices to ensure accuracy and reliability. Collaborate across teams to transform data for analytics and innovation, drivin...

Accelerate progress at the forefront of Global Health Economics, leveraging Real-World Evidence to drive patient access and optimize pricing strategies. Collaborate across teams to implement evidence...

Lead the charge in refining development assurance processes to improve compliance with ARP4754B. Collaborate with systems engineering to enhance requirements management across all program phases while...

Empower growth through technical sales in gene therapy, driving new business and enhancing customer experiences. Collaborate with Central Sales to manage accounts and leverage technical insights for l...