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8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer. Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Support the Public affairs team’s writing and material production to educate internal and external stakeholders on the impacts of current and proposed regulatory and legislative changes. Under the direction of VP, Public Affairs, the Strategic Relationship Lead, External affairs acts as a key member of the Government Relations and Public Affairs team’s efforts to build strength to impact public policy on behalf of Novant Health.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Work in the Global Rare Diseases, Regulatory Affairs Ad Promo function for the United States, with additional duties in Canada. Minimum 5 years Pharmaceutical/Biotechnology industry experience, at least 3 years Regulatory Affairs and advertising and promotion review and approval experience with marketed prescription drugs.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Shape, lead & advance US regulatory policy & advocacy efforts of interest to UPL in enabling US grower access to innovative technologies. Regulatory experience with US federal and state government interaction as well experience interacting with the EPA needed.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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At least ten years of experience within Regulatory Affairs of which at least five in the global context. Knowledge of the drug development process, of drug regulations, regulatory procedures and drug development guidance.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Regulatory Affairs Specialist coordinates the regulatory activities for life cycle management of marketed pharmaceutical products. Additionally, the role will assist in organizing submission of Advertising and Promotional pieces to FDA. These obligations will also require interactions with the Regulatory Operations team to plan, prepare, and complete accurate and timely submissions to Heath Authorities.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This position is part of Quality and Regulatory Affairs located in Fargo, ND and will be fully remote. The Director of Global Regulatory Affairs will be responsible for developing and executing regulatory strategies for drug development and commercialization ensuring compliance with global regulations and standards across multiple markets.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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At least 10 years’ experience in Regulatory Affairs, with direct experience in Labeling and Advertising/Promotional review. Create/revise SOP’s and Work Instructions as applicable, to ensure high performing regulatory operations and effective review processes.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The Regulatory Affairs Specialist will assist in providing regulatory services to management for the Global Regulatory Affairs (GRA) group throughout the functional operations of improving entire drug development and commercialization process in areas including document authorship and review, preparation of applications for global submission, authorship and review to deficiency responses, and maintaining current regulatory practices and expectations.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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In the role of Senior Director, Regulatory Affairs, you will be responsible for overseeing and directing regulatory activities for new and mature products to ensure alignment and compliance with local and regional registration requirements as well as with company policies.
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Are you an excellent collaborator with the desire to learn more about regulatory affairs supporting the Investment Bank and Wealth Management business? The US Securities Regulatory Affairs team handles regulatory examinations, inquiries, investigations and enforcement actions conducted by securities regulators such as the SEC, FINRA and others, as well as promotes and manages effective relationships with key US regulators.
$92,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Global Regulatory Affairs CMC & Device organization is responsible for global CMC regulatory strategies and activities for the PDT BU product portfolio through clinical development, market launch and product lifecycle management.
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This role shall be the primary spokesperson for state legislative and regulatory matters and will lead external engagement with state governments across the USA. Additionally, the person in this role will be responsible for managing JTI's relationships with associations and collaboration with other stakeholders on state developments.
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Bachelor’s degree in life sciences, engineering, or a related field; advanced degree (e.g., Master’s, PhD) or regulatory affairs certification (RAC) preferred. Team Leadership and Development: Lead, mentor, and develop a high-performing regulatory affairs team.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Proclinical is seeking an (Associate) Director, US Regulatory Affairs, Advertising & Promotion for a large global pharmaceutical company with locations in Georgia, North Carolina and Massachusetts.
Full-timeExpandApply NowActive JobUpdated 1 month ago
regulatory job Title: affairs in Raleigh, NC
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