Regulatory Affairs Manager Jobs in Newark, NJ

The Manager, Promotional Review at Johnson & Johnson will lead the execution of promotional review processes, ensuring compliance and quality in the approval of marketing assets. This role involves co...

The Director of Global Regulatory Affairs is responsible for interpreting and advising on federal, state, and international regulations related to products and processes. This role involves ensuring c...

The Senior Director, Regulatory Affairs Global Strategy Implementation at Johnson & Johnson is responsible for setting strategic direction and priorities for product registration and regulatory compli...

The Associate Director - Global Regulatory Lead will lead a global regulatory team to develop and execute regulatory strategies for high-impact projects involving innovative investigational medicines...

The Senior Specialist in Regulatory Affairs is responsible for coordinating and preparing document packages for regulatory submissions, ensuring compliance with domestic and international regulations...

The Sr Manager of Regulatory Affairs & Compliance will oversee and advance FreedomCare's compliance program, ensuring adherence to healthcare regulations and managing risks. This role involves leading...

The Sr. Manager, Regulatory Operations is responsible for managing regulatory submission activities, including document publishing, submission assembly, and compliance review. This role requires exper...

The Manager - US Regulatory Relations is responsible for managing relationships between American Express and U.S. regulatory agencies, ensuring operational excellence in regulatory interactions. This...

The Senior Manager, Quality Management Systems will oversee compliance and regulatory activities within the Quality Assurance department at Catalent Pharma Solutions. This role involves managing audit...

The Director, Global Regulatory Leader is responsible for developing and implementing global regulatory strategies for oncology projects. This role involves leading the Global Regulatory Team, ensurin...

The Associate Director, Regulatory Affairs Strategy will lead and support clinical development programs as the Regulatory Lead, focusing on regulatory strategy and execution activities for drug submis...

The Manager, Regulatory Compliance will be responsible for implementing a compliance framework and providing regulatory advice related to derivatives and financial products. This role involves staying...

The Environmental Chemical Regulation Manager at LG Electronics is responsible for monitoring and analyzing environmental regulations related to hazardous substances, refrigerants, pesticides, and oth...

The Product Management Senior Manager of Regulated Markets Audit is responsible for leading a team that manages Government Audits and issue management for Regulated Markets. This role involves strateg...

The Quality Assurance Manager oversees the Quality System for multiple Environment, Health, & Safety labs in the US, ensuring regulatory compliance and leading QA functions. This role involves conduct...

The Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for managing and optimizing global business processes within Regulatory Affairs and Clinical Safety. This role invo...

The Project Manager (RACMC) is responsible for leading and supporting complex regulatory filing activities, ensuring compliance with technical and regulatory standards. This role involves efficient re...

The Senior Manager of Regulatory Affairs Systems and Operations will oversee the development, implementation, and maintenance of the global BDX Regulatory Information platform. This role involves mana...

The In-Process Quality Assurance Manager is responsible for overseeing quality assurance inspections and managing the Quality Inspection team to ensure compliance with cGxP standards. This role involv...

The Manager, R&D Quality Assurance will support Global and Regional Quality Leads in ensuring compliance within R&D programs, particularly in oncology and specialty medicine. This role involves monito...

The CMC Regulatory Specialist (Associate Principal Scientist) is responsible for developing and managing CMC regulatory submission strategies and timelines for pharmaceutical projects. This role requi...

The Director of US Regulatory Affairs Strategy will lead the preparation and submission of regulatory documents to the FDA, ensuring timely and quality submissions to facilitate the approval of pharma...

The Associate Director Regulatory Affairs, Advertising and Promotion will serve as an internal expert on U.S. FDA regulations and provide commercial regulatory strategy and leadership. This role invol...

Lead QA strategy for assigned brands by studying product requirements; analyzing options for product stability and process validation; recommending, preparing, and presenting corrective action plans...

The Quality Assurance (QA) Sr. Manager will hold a key position in our Quality & Regulatory Affairs Department. This individual will support existing products and new product introductions in sterile...