Global Regulatory Lead
3 weeks ago
A global pharmaceutical company is seeking an experienced Associate Director of Regulatory Affairs. This role requires managing regulatory activities within a Global Regulatory Team and leading the strategy development for product registration. Candidates should have at least 7 years of experience, including 4 years in regulatory affairs, alongside strong communication and organizational skills. The position offers a competitive salary and comprehensive benefits in a dynamic environment.
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Global Regulatory Labeling Lead — CCDS
3 weeks ago
Dover, United States Parexel Full timeA leading global biopharmaceutical firm is seeking a detail-driven Senior/Consultant in Regulatory Labeling based in Dover, DE. In this high-impact role, you'll lead global labeling efforts ensuring compliance and improving product communication. Ideal candidates will have a Bachelor's Degree and 4+ years’ experience in drug development, especially in...
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Dover, United States Delaware Staffing Full timeChemistry, Manufacturing and Controls Global Regulatory AffairsThe Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs professional is responsible for developing and executing global regulatory strategies for CMC aspects of small molecule products during late-stage development and throughout the commercial lifecycle. This includes initial...
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Global Oncology Regulatory Leader — NDA
3 weeks ago
Dover, United States Sumitomo Pharma Full timeA global pharmaceutical company is seeking a Vice President of Regulatory Affairs Oncology in Dover, Delaware. This leader will drive regulatory strategy for oncology therapies, leveraging over 15 years of biopharmaceutical experience. Key responsibilities include managing regulatory submissions and ensuring compliance with FDA regulations. The ideal...
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Associate Director, Regulatory Affairs
3 weeks ago
Dover, United States Delaware Staffing Full timeAssociate Director Regulatory AffairsSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies, and CNS. With several marketed products and a diverse pipeline of early-...
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Associate Director, Regulatory Affairs
5 days ago
Dover, United States Delaware Staffing Full timeAssociate Director, Regulatory Affairs (Oncology)Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies, and CNS. With several marketed products and a diverse...
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Associate Director, Regulatory Affairs
6 days ago
Dover, DE, United States Sumitomo Pharma Full timeSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets,...
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Associate Director, Regulatory Affairs
1 week ago
Dover, DE, United States Sumitomo Pharma Full timeSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets,...
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Associate Director, Regulatory Affairs
2 weeks ago
Dover, DE, United States Sumitomo Pharma Full timeSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets,...
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Dover, United States Sumitomo Pharma Full timeA leading global pharmaceutical company is seeking an Associate Director of Regulatory Affairs in Dover, Delaware. This role involves managing regulatory submissions and providing strategic regulatory input for oncology products. Ideal candidates should have a bachelor's degree, substantial experience in the biopharmaceutical industry, and specific...
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CMC Regulatory Affairs Senior/Consultant
5 days ago
Dover, United States Delaware Staffing Full timeCmc Regulatory Affairs Senior/ConsultantExciting opportunity for an experienced and highly motivated professional to join our global regulatory affairs team. This role is critical to ensure our client's investigational, new, and marketed small molecule products are developed and maintained in compliance with global regulatory requirements. The primary...