We currently have an opportunity for a Safety Assurance/Regulatory Affairs Associate within the Fragrance division located in Rockleigh, NJ. Communicate with suppliers on requests for safety/regulator...
read moreMore Years of direct regulatory affairs experience, including US labeling experience required. This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently pro...
read moreWe currently have an opportunity for a Safety Assurance/Regulatory Affairs Associate within the Fragrance division located in Rockleigh, NJ. Provide assistance to perfumers on safety/regulatory requir...
read moreReporting to the Director in Organon Regulatory Chemistry, Manufacturing and Controls New Products, the Associate Principal Scientist (Associate Director) is responsible for Regulatory Chemistry, Manu...
read moreThe individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that...
read moreHave worldwide responsibility for CMC-regulatory aspects of Development Projects, Strategic Products, Established Products, and Strategic Projects requiring extraordinary regulatory expertise within G...
read moreAssociate Director, Global Regulatory Affairs Labeling. This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leaders...
read moreSenior Manager/Associate Director, Global Regulatory Affairs, Labeling Strategy. The Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development a...
read moreThe individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that...
read moreThis 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 Reg...
read moreMore Years of direct regulatory affairs experience, including US labeling experience required. This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently pro...
read moreMore Years of direct regulatory affairs experience, including US labeling experience required. This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently pro...
read moreThe Regulatory Affairs-Labeling, Associate Director is responsible for ensuring that Takeda gains regulatory approval for new products and product amendments, while maintaining the currency of product...
read moreThis 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 Reg...
read moreMore Years of direct regulatory affairs experience, including US labeling experience required. This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently pro...
read moreEnsures the CMC development and commercial product regulatory strategy meets global regulatory requirements over the lifecycle of the product and is in alignment with the strategies of global regulato...
read moreDirects and prepares global regulatory affairs strategies and executes regulatory activities for Taiho Oncology, Inc. Associate Director, Regulatory Affairs Strategy. Ten years previous experience in ...
read moreResponsible for understanding the regulatory landscape, assessing regulatory risk, and developing global filing strategies. Ensure global development plans will meet global regulatory requirements by ...
read moreEnsure global development plans will meet global regulatory requirements by soliciting and integrating regional regulatory strategy liaison input. Responsible for understanding the regulatory landscap...
read moreThe Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development and maintenance of global labeling documents (e. This role will be within Global R...
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