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We are currently seeking a Regulatory Affairs Associate Director/Director to join our growing regulatory team. 5 – 7 (Director)/ 7 – 9 (Associate Director) years of experience in Regulatory Affairs (strong preference for experience in oncology) in the biotechnology or pharmaceutical industries, including an in-depth knowledge and understanding of the regulatory environment.
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Proclinical is seeking an Associate Director, Regulatory Affairs, Advertising & Promotion for a global pharmaceutical company with their location in New Jersey. Associate Director, Regulatory Affairs, Advertising & Promotion - Permanent - New Jersey.
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Director, CMC Regulatory Affairs. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
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NY Green Bank (“ NYGB ”) seeks a senior attorney (the “ MD-L&R ”) to join its management team, lead its Legal & Regulatory Affairs (“ LRA ”) team and provide legal advice and strategic counsel with respect to NYGB’s operations, transactions, regulatory issues, and general corporate affairs.
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As the Regulatory Affairs Director, you will have the opportunity to lead Allogeneic trials – the most innovative in history! Director, Regulatory Affairs. 10+ years of Regulatory Affairs experience within a pharmaceutical or biotech setting.
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Bachelor's degree in a relevant life sciences field with at least 8 years of experience in the biopharmaceutical industry, particularly with biologics and regulatory affairs. They are seeking a dynamic Director of Regulatory Strategy to steer our groundbreaking projects through the complex regulatory landscape with vision and precision.
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They are looking for a Director or Senior Director of Clinical Regulatory Affairs to join their team. Director/Senior Director, Regulatory Affairs.
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As Director - Regulatory Affairs US , you will be instrumental in establishing Nordberg Medical's presence in the US market, supporting our FDA PMA approval process. You will collaborate extensively with our Clinical Affairs Director, Chief Quality & Regulatory Affairs Officer and Senior Advisor to ensure seamless coordination and success in our regulatory endeavors in the US.
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They are looking to bring on a Senior Director, Regulatory Affairs to the team. Experience in leading regulatory affairs across multiple major geographic areas and handling both small molecules and biologics.
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5 – 7 (assoc dir)/ 7 – 9 (director) years of experience in Regulatory Affairs (strong preference for experience in oncology) in the biotechnology or pharmaceutical industries, including an in-depth knowledge and understanding of the regulatory environment.
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We are leaders in regenerative medicine, and hiring a talented Regulatory Affairs Director to lead and drive innovation within our growing team. As our Regulatory Affairs Director, you will be the driving force behind our regulatory strategies, ensuring compliance with FDA, state requirements, and AATB Standards.
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Due to an accelerated growth trajectory, the client is looking for a Senior Director Regulatory Affairs who as a member of the leadership team will help make decisions that are critical at this time.
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An innovative privately held medical device firm is looking for a Director of Regulatory Affairs. Job title: Director of Regulatory Affairs - Medical Devices.
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My client is seeking a Director, Regulatory Affairs to join their Regulatory team. At least 8-10+ years of Regulatory Affairs experience. Extensive global regulatory submission experience (IND/CTA/BLA/NDA.
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Provide overall company leadership and direction for worldwide Tecomet Quality Assurance and Regulatory Affairs Systems, encompassing both improvements and sustaining activities. Six Sigma Black Belt certification (desirable but not essential.
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Title: director regulatory affairs in New York, Norwood, Massachusetts
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