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. Communicate with customers on safety and regulatory issues....
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 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 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 moreHave worldwide responsibility for CMC-regulatory aspects of Development Projects, Strategic Products, Established Products, and Strategic Projects requiring extraordinary regulatory expertise within G...
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 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 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 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 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 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...
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...
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