- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently ... provides strategic and operational leadership on product labeling in collaboration with Global ...pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling… more
- Genmab (Plainsboro, NJ)
- …and authentic is essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible ... Genmab portfolio of products. This role will be within Global Regulatory Affairs (GRA) and...Affairs (GRA) and will report to the Sr Director , Labeling , Policy and Intelligence. The position… more
- Genmab (Plainsboro, NJ)
- …authentic is essential to fulfilling our purpose.The RoleGenmab is looking for an Associate Director , Global Regulatory Affairs , Regulatory Strategy ... to be a part of our Global Regulatory Affairs organization.In this role, you will... success. Represent US RA in the Global Regulatory Team, Labeling Working… more
- Genmab (Plainsboro, NJ)
- …is looking for an experienced and passionate leader to be a part of our Global Regulatory Affairs (GRA) organization.In this role, the regulatory ... to the Team Lead of Regulatory Strategy, Global Regulatory Affairs , the key...regulatory requirements for programs and products. Participate in regulatory sub-team, clinical management team, and labeling … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. SummaryThis position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global ... new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety...of contact for cross-functional teams on RA labeling issues. Collaborate with Regulatory Affairs… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. Summary This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global ... new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety...of contact for cross-functional teams on RA labeling issues. Collaborate with Regulatory Affairs… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …Management Cross-Functional Team (GLOC)** + In alignment with Head, Global Regulatory Affairs Marketed Products and Labeling , coordinates the process ... patients with immunologic, hematologic, and other complex diseases. The Director , Global Labeling Strategy Lead...Management** + Appropriately escalates issues to Global Labeling management and the Global Regulatory… more
- Integra LifeSciences (Princeton, NJ)
- …new treatment pathways to advance patient outcomes and set new standards of care. The Director , Global Regulatory Labeling is responsible for overseeing ... affairs and quality assurance and working knowledge of global regulatory labeling requirements in key markets/geographies. + Ability to multi-task… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …around rare diseases and immune disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently ... provides strategic and operational leadership on product labeling in collaboration with Global ...experience required + 4 or More Years of direct regulatory affairs experience, including US labeling… more
- Sumitomo Pharma (Trenton, NJ)
- … Regulatory Affairs ** . The Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will primarily function ... as the Regional Regulatory Leader (RRL) and/or Global ...pharmaceutical industry with minimum of 8 years focused in regulatory affairs . + Master's degree required (preferably… more
- Bristol Myers Squibb (Princeton, NJ)
- …more: careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of ... + Ensure global development plans will meet global regulatory requirements by soliciting and integrating...with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …rare diseases and immune disorders. **Summary** This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global ... new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety...of contact for cross-functional teams on RA labeling issues. Collaborate with Regulatory Affairs… more
- J&J Family of Companies (Raritan, NJ)
- Johnson & Johnson Innovative Medicine is recruiting for a Director , Global Regulatory Leader. This position can be located in Spring House, PA; Horsham, PA; ... potential. At Johnson & Johnson, we all belong. The Director , Global Regulatory Leader, is...and medical affairs programs. + Provide integrated global labeling and filing strategies for assigned… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , Marketing, ... well as other labeling documents. + Demonstrate knowledge of local and global health authority requirements. + Support GPSE in the maintenance of a highly… more
- Integra LifeSciences (Princeton, NJ)
- …brochures and seminars + Monitors product development progress with engineering, manufacturing, regulatory affairs and related departments to ensure product line ... new standards of care. ** Global Senior Product Manager** Reporting to a Senior Director , Global Marketing - Codman Specialty Surgical, CSS, the Global … more
- Integra LifeSciences (Princeton, NJ)
- …brochures and seminars + Monitors product development progress with engineering, manufacturing, regulatory affairs and related departments to ensure product line ... patient outcomes and set new standards of care. Under direct supervision of a Director , Global Marketing - Codman Specialty Surgical, CSS, this role will… more
- Bristol Myers Squibb (Princeton, NJ)
- …and FDA guidelines. The role works closely with the Proofreading team, Labeling Operations, Commercial Regulatory Affairs , and Worldwide Commercialization ... documents per specifications. + Develop artwork and illustrations as required for Global Regulatory , Packaging, and R&D. + Develop and maintain Universal… more
