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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.
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Shape, lead & advance US regulatory policy & advocacy efforts of interest to UPL in enabling US grower access to innovative technologies. JOB SUMMARY: UPL is seeking an experienced Government Affairs & Industry Relations leader to be responsible for engagement with US Federal and State government, grower organizations and industry/trade associations to influence outcomes affecting the UPL NA business as well as support policy and legislative activities through industry partnerships.
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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.
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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.
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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.
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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.
$150,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days 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.
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Motivate and guide the professional development of the Legislative Affairs Associate reporting indirectly to the incumbent; The State Government Affairs Manager shall be responsible for leading public affairs strategies geared to support the mission and advocacy goals of JTI USA. This shall include developing and executing state-level advocacy material and plans.
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Piper Companies is searching for a Regulatory Affairs Manager for Advertising & Promotion to join the regulatory affairs team of a global biopharmaceutical company. 1+ years demonstrated regulatory affairs experience within US regulatory advertising and promotion.
$120,000 - $135,000 depends on experienceFull-timeExpandApply NowActive JobUpdated Today - 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.
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We are working on a retained search, Director, Global Regulatory Affairs position with a growing pharmaceutical company that is in the areas of rare-disease/immunology/autoimmune diseases.
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Join our dynamic Regulatory Affairs team and contribute to our mission to enable our customers to make the world healthier, cleaner and safer. As Sr. Manager, Regulatory Affairs , you will assume a key role in the interpretation and dissemination of global regulations, guidelines, and emerging industry developments that directly influence our business.
$140,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Director, Regulatory Affairs is responsible for assisting with establishing and managing regulatory strategies, life cycle plans, and pre/post regulatory approvals. Establish regulatory strategies and process by collaborating and coordinating with relevant development and CMC team members.
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Mix Talent has partnered with a global medical aesthetics company to be their exclusive recruiting partner and support the search for their next Regulatory Affairs Senior Specialist, Medical Devices.
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Atlantic Medical Management (AMM) is seeking an Regulatory Affairs Assistant. The Regulatory Affairs/Support Assistant will perform a variety of responsibilities to support Regulatory Affairs/Compliance department within AMM. Their primary focus will be maintaining internal regulatory procedures related to exclusion screenings, employee user accounts, provider directory listings, and other administrative duties as required.
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regulatory affairs jobs Title: affairs in Raleigh, NC
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