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 Reg...
read moreWe currently have an opportunity for a Safety Assurance/Regulatory Affairs Associate within the Fragrance division located in Rockleigh, NJ. Two (2) years of experience in regulatory or product safety...
read moreWe currently have an opportunity for a Safety Assurance/Regulatory Affairs Associate within the Fragrance division located in Rockleigh, NJ. Conduct safety review of fragrance formulas according to in...
read moreYou will report to the Senior Director of Regulatory Affairs CMC and be part of the Regulatory Affairs CMC team consisting of 8 experienced and dedicated colleagues. The project portfolio at Genmab is...
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 moreThis includes assessing CMC changes during development and defining regulatory CMC requirements, demonstrating sound regulatory insight, ensuring a balanced approach to regulatory risk, utilizing regu...
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 moreTanner and Associates is recruiting an Associate Director, Regulatory Affairs, Advertising & Promotion for a Pharmaceutical Company. Represents Regulatory Affairs on the company’s Promotional Review C...
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 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 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 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 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 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 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 moreMaintain current expertise on developments in the assigned therapeutic area from the global regulatory, legislative, scientific, medical, pharmaceutical, pharmacovigilance, market access and commercia...
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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