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Industry Issues Analysis:Implement advanced tracking and analysis of key agricultural and food production issues and influencers with an emphasis on animal care (especially dairy), farm policy, food policy, environmental stewardship in food production, food/beverage animal ag/dairy activism.
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The Executive Director, Regulatory Affairs will develop and execute global regulatory strategic and tactical guidance for the development of innovative new drugs in rare disease ensuring fast to market global product registrations, product promotion, maintenance of products and processes in regulatory compliance with local regulations.
$315,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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. Provides guidance on regulatory requirements and strategies to software product development project teams.
$218,500 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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A minimum of 6- 10 years’ experience in product stewardship, regulatory affairs, compliance, chemical consultancy, and/or risk assessment. Manage external advisors and consultants on product stewardship, chemical regulatory compliance, and sustainability matters.
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3+ years of relevant experience in Regulatory Affairs/Product Stewardship role in the chemical industry. Flint Group is seeking a Regulatory Affairs Specialist to ensure continuous compliance for industrial ink and coatings products, supporting commercial teams in North America.
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Represent MedTech Product Stewardship on the Enterprise Packaging EPR Community of Practice (COP). We’re seeking an experienced Product Stewardship Specialist – Global Environmental Packaging.
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Job Title: Regulatory Affairs Specialist. Reporting to: Regulatory Affairs Manager, Americas. Department: Product Regulatory Compliance. Implement regulatory strategies related to regional regulatory changes (e.g., Prop 65, TSCA, DSL, FDA, CMP, etc.
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Collaborate across Process Development, Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs, Finance and Technical Development for successful commercialization of late-stage portfolio.
$328,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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More details on our benefits can be found on our website at 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 8 days ago - UpvoteDownvoteShare Job
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What we look for: A scientific degree with directly relevant professional experience in global CMC regulatory affairs and CMC technical areas of at least 20 years with a BA/BS, MA/MS, PhD or PharmD. Demonstrated organizational leadership skills at both functional and enterprise levels.
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Serve as the PDM regulatory representative on project teams, provide CMC regulatory support for the clinical development of the investigational product(s), and ensure applicable regulatory requirements are appropriately met.
$113 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Environmental & Sustainability Compliance Manager- Chemical will be responsible for providing global support to multiple functions through the implementation of product stewardship processes related to product chemical compliance and sustainability activities.
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Provide PV leadership for Jazz Pharmaceuticals Clinical Development including Clinical, Investigator Sponsored, Compassionate Use, and Disease Monitoring Programs; liaise with Clinical Sciences, Clinical Operations, Medical Affairs, Biometrics, Regulatory Affairs, Contract Research Organizations (CROs), Data Monitoring Committees (DMCs) and other entities to contribute to overall study execution while ensuring safety strategy and operational excellence.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Minimum of 10 years of experience in regulatory affairs with a strong focus on Chemistry, Manufacturing, and Controls (CMC). Provide regulatory input on product development plans, manufacturing changes, and quality control processes to ensure compliance and mitigate regulatory risks.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Represent CMC regulatory affairs on product teams and in health authority interactions. This position is hybrid, and based in Santa Monica, CA and reports to the Executive Director, CMC Regulatory Affairs.
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regulatory affairs specialist on site product stewardship jobs
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