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Your role Manages F&B Naturals Regulatory Affairs team and and coordinates with F&B Flavor Regulatory Affairs team to ensure regulatory compliance of Naturals products with corporate guidelines and government regulations.
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Chemistry, Manufacturing and Controls (CMC) Regulatory Affairs Managers. Direct/indirect Regulatory Affairs CMC experience with submissions for synthetic and/or biologic and biotechnology derived products such as monoclonal antibodies or complex biologic products.
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Regulatory Affairs & Customer Service Manager - Agri-Input Dept. - Agri Input Unit. Manages Regulatory, IP, and Compliance Affairs. Manages contracted specialists, local sales personnel, and/or overseas office team for product and trademark registration and regulatory requirement, updates, and maintenance to keep them in good standing while coordinates with regulatory department of the vendors for data collection, commissions tests for dossier development.
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Coordinates with the Controller Account Specialist and the DM General Manager of Operations to ensure efficient customer service through effective selection and consolidation of carriers, warehouses, custom brokers, etc.
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BioTalent is representing a top-tier life sciences device manufacturer hiring a Regulatory Affairs Manager ensure compliance with global regulatory requirements while managing the regulatory affairs team.
ExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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The Regulatory Affairs Manager is responsible for oversight, planning, and management of registration submissions with a focus on Global product registrations. The Global Regulatory Affairs Manager directs Global regulatory package/dossier development, product registration, and lifecycle management of all Certis Biologicals products.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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ISK Biosciences Corporation is seeking a Regulatory Affairs Manager who would be primarily responsible for the registration, regulatory compliance and development of ISK Biosciences products in North America.
ExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Minimum seven (7) years customs brokerage, customs consulting, regulatory or similar professional services is required. Actively manage and continuously develop a team of compliance professionals providing day to day support of regulatory and compliance-based inquiries.
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The Senior Manager/Director of Policy and Regulatory Affairs will be responsible for managing the company's relationships and policy positions at PJM, federal and state regulatory agencies, and state legislative bodies.
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My client is a multinational CDMO looking for a Regulatory Affairs Manager to work with the FDA and their client sites to manufacture generic APIs, drug products, and certain med devices.
ExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Could you be our next Senior Manager of Regional Regulatory Affairs? Be a GRA NA representative for assigned projects to the Global Regulatory Affairs Strategy Team (GRAST) to provide regional input into the delivery of science-based and globally aligned regulatory strategy with GRL.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Regulatory & Medical Affairs - Regulatory Studio - CMC Senior Manager. Work with CMC cross-functional teams and Regulatory Affairs teams. Participate in the development of the CMC regulatory strategy for post-approval small molecule product submissions, including global supplements/variations and responses to health authority queries.
ExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Senior Manager, Regulatory Affairs: Base Salary Range $120,000 - $150,000. We are actively recruiting for a Senior Manager, Regulatory Affairs who will lead the development and execution of regulatory strategies through a program’s lifecycle.
$120,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Master’s degree in a scientific field is required with emphasis on regulatory affairs and in the dietary supplements category. § Seven -plus years of experience in a regulatory role having oversite to compliance and involvement in QMS in the nutrition and dietary supplement categories.
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This position will provide Regulatory Affairs oversight to Laerdal to assure FDA and Health Canada medical device and establishment requirements are met and both Laerdal Medical Corporation (LMC) and Laerdal Medical Canada (LMCA) remain compliant to medical device regulations.
$95,000 - $105,000 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago
regulatory affairs jobs Title: regulatory affairs manager in Ridgefield, NJ
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