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The TeamAmongst its other responsibilities, the Global Strategy, Regulatory and Public Affairs team leads on the development and implementation of Gates Ag One's regulatory science programs and related activities, such as regulatory studies, permit acquisition, and ensuring compliance with phytosanitary and biosafety regulatory requirements.
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Prior experience at a major law firm, in-house legal department of a financial institution and/or bank regulatory agency. Knowledge of relevant regulatory agency rules and regulations essential to this position (e.g., OCC, FRB, CFPB, and FINRA.
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Coordinate and communicate timelines and deliverables with Regulatory Operations, Labeling and other key departments to facilitate quality CMC and safety-related regulatory submissions, including ANDAs, Amendments, Annual reports, PSUR and post approval Supplements.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Possess thorough experience in analyzing legislative and regulatory tax developments, IRS regulatory process and procedures, performing legal research, and writing and interpreting complex legal opinions, as well as understanding the applicability and precedential value of judicial decisions and IRS published guidance such as regulations and revenue rulings involving federal tax law.
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Our team in St. Louis currently has an opening for a Safety, Regulatory, Quality Site Coordinator. Ensure that required regulatory reporting requirements are met. Ensure that all required regulatory and safety training is kept up to date.
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At least 1 year of experience within regulatory affairs. Position is also responsible for assembling and maintain technical files and other regulatory documentation to ensure timely registrations and renewals.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Manage regulatory review for CAPA investigations, adverse events, validations, and general projects (removed printed materials & added adverse events) With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and changes to products or sale of products ensuring continual compliance to all applicable regulations and ensuring that site regulatory strategy aligns with overall corporate regulatory strategy, goals, and objectives.
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Research and decipher regulatory sources such as legislative rules, federal registers, and bulletins regarding payment rules for Medicare as well as deciphering contractual language regarding commercial payment arrangements.
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This role would have direct responsibility for all compliance aspects of the organization (15-20 people) including Regulatory Affairs, Quality Assurance, Quality Control, Document Control and Safety and reports to the CEO.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Authoring, reviewing, and commenting for Chemistry Manufacturing and Control (CMC) CTD documents for biologics products, including Investigational Applications (IND, CTX), Marketing Applications (NDA, NDS, MAA, BLA), and post-approval lifecycle dossiers, gap analyses and responses to review questions per the Regulatory Affairs Services Menu.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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2+ years of professional experience in Regulatory Affairs (IVD) Independently assemble and maintain technical files and other regulatory documentation to ensure timely registrations and renewals.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Job Title: Regulatory Affairs Specialist. Job Title: Regulatory Affairs Specialist. Bachelor's or Master’s degree in Pharmacy, Chemistry, Biology, Engineering, or other Life Science discipline. Location: 63103, St Louis, Missouri, United States.
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Regulatory Affairs Expert-Medical Devices. Support any recall or notification actions and carry out regulatory vigilance reporting as required. Respond to internal and external customer regulatory requests and/or inquiries.
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Is seeking to hire a Quality & Regulatory Affairs for our client in St. Louis, MO! Support preparation for and participate in audits by regulatory bodies. is seeking to hire a Quality & Regulatory Affairs for our client in St. Louis, MO.
$33.5 an hourExpandUpdated 10 days ago - UpvoteDownvoteShare Job
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Demonstrated experience in regulatory filings and support for CGT/ATMP products. Job Summary The Senior Manager, Regulatory Affairs position will support the Regulatory Affairs (RA) Director to help define the regulatory strategy for our innovative next-generation technology for cellular therapy.
RemoteExpandApply NowActive JobUpdated 8 days ago
Title: regulatory Company: Coda Searchstaffing in St Louis, MO
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