The 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...

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...

This includes assessing CMC changes during development and defining regulatory CMC requirements, demonstrating sound regulatory insight, ensuring a balanced approach to regulatory risk, utilizing regu...

We 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...

Senior 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...

The 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...

The 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...

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...

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...

More 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...

The 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...

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...

The 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...

Assures connectivity to the overall global regulatory strategy through partnership and communication with Therapeutic Area Regulatory Affairs (Global Regulatory Leader). Ensures the CMC development an...

The 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...

Ten years previous experience in global regulatory affairs and regulatory submissions for drugs, preferably in oncology. Associate Director, Regulatory Affairs Strategy. Directs and prepares global re...

The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing commercial regulatory strategy and leadership to enable the US business to meet its commercial needs i...

The 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...

Responsible for understanding the regulatory landscape, assessing regulatory risk, and developing global filing strategies. US Medical Device Regulatory Affairs experience. Ensure global development p...