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Support development of strategies to improve effectiveness and efficiency of overall regulatory and scientific affairs environment. 5+ years of experience in the food and/or dietary supplements regulatory environment with full expertise on regulatory compliance (i.e. product composition; DSHEA; ingredient qualification, e.g., GRAS, NDI; labeling; Health Claims & Structure/Function Claims; overall product communications.
$150,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Associate Director (Associate Principal Scientist), Organon Manufacturing & Supply (OMS), Chemistry, Manufacturing & Controls (CMC), Network Project & Resource Management will provide regulatory CMC support for Organon Network Projects.
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Title: Regulatory Affairs and Product Stewardship (RAPS), Pharmaceutical Solutions (PhS) Director. In the Global Regulatory Affairs (GRA) team we have an opening for a Regulatory Affairs and Product Stewardship (RAPS) PhS director to lead the global regulatory team supporting the PhS business, and to drive regulatory activities for our ~$1B Pharmaceutical Solutions portfolio of businesses.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Blackrock Neurotech, a leader in neurotechnology, is seeking an experienced and visionary Head of Regulatory Affairs to design and execute global regulatory strategies for our Brain-Computer Interface (BCI) platform technology and its applications.
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Reporting to the Chief Compliance Officer, the Assistant General Counsel - Regulatory Affairs provides legal support to each of ITW's Segments and Corporate functions as needed on a variety of regulatory matters, with a principal focus on monitoring and advising ITW businesses regarding existing and developing legal and regulatory issues affecting the company's operations and products.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Affiliate Government Affairs; Affiliate Public Affairs; Regulatory Affairs; Legal; OEC. Professional experience as role of Medical affairs or in a similar field-based R&D role (Clinical trials and clinical development) for at least 3+ years for MSL and 5+ for Sr. MSL.
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The VP leads a team of professionals across multiple cities to influence the regulatory affairs/advocacy agenda for hydrocarbons and biofuels, owns key strategic relationships internally with the Communications & External Affairs team and externally with various trade associations, and promotes the physical regulatory reporting responsibilities for all commodities (a key license-to-operate function.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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10+ 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 and small molecules.
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Develop effective collaborations with research project leaders and projects team members, including biostatistics, regulatory affairs, clinical pharmacology, clinical scientists and development operations.
$423,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Relevant professional experience includes government, private sector, commercial contracting, or regulatory affairs, international development, international business, or finance with an emphasis on contract and/or grant management cost analysis and pricing, management consulting, or public and/or nonprofit administration.
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Reporting to the AGC will be a Regulatory Affairs team, a Trade Compliance team and a Legal Compliance Specialist. The AGC will manage outside counsel relationships for Labeling Litigation/Disputes, Regulatory, and Trademark and Intellectual Property matters.
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This individual will work collaboratively with members of all departments within the company, including but not limited to Offshore Wind Development, Onshore Development, Origination, Transmission, Regulatory, and Environmental Compliance & Strategy.
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This Regulatory Affairs Manager – Digital Health Technology will work on-site at our Alameda, CA location in the Diabetes Care Division. This Regulatory Affairs Manager – Digital Health Technology will provide support for the regulatory department to ensure efficient and compliant business processes and environment.
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Deep understanding of state legislative, regulatory, and political campaign processes. Work with the Managing Director to prepare and present information and recommendations to the VP, State Government Affairs and the SVP, Government Affairs.
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Policy Advocacy: Lead lobbying efforts on specific healthcare proposals and bills, influencing legislation and regulatory issues to align with company interests. Job Summary:The Director of LATAM Government Affairs will have the unique opportunity to leverage their expertise and leadership skills, working with a diverse team to influence and shape public policy across Latin America.
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regulatory affairs jobs Title: travel rn Company: Medical Solutions in Amarillo, Texas
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