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Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
$103,500 - $170,800 a yearFull-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Perform duties as an instructor for National Incident Management System and preparedness courses with concentration in the following functions: Emergency Management (EM), Law Enforcement, Fire Emergency Services, Emergency Medical Services (EMS), and Public Affairs.
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Serving as a field resource for The Medical Affairs Company (TMAC), the Clinical Trial Liaison (CTL), reporting as Early Clinical Liaison , will represent the Company’s Respiratory Clinical Development program.
$150,000 - $160,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Seekinformation fromthe Director of Regulatory Affairs and External Affairs teamsregarding legislative and regulatory updates and be part of working group to ensure they are interpreted and executedappropriately acrossthenetwork.
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Processes new studies for internal review and serves as the contact for completion and collection of the regulatory affairs questionnaire for Sponsors/Contract Research Organizations (CRO.
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Currently seeking a new Global Director of Regulatory Affairs to help spearhead our client's 1st generation PMA submission as well as future supplements and OUS international registries for global commercialization.
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Responsible for adhering to all legal, regulatory and HCC policies to including AdvaMed, Pharma, ACCME, Sunshine Act, etc. In collaboration with others in Office of Medical Affairs, works to ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
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In support of public affairs, leads and/or partners in the development and implementation of all communications to include crisis management, legislative, regulatory and litigation communications.
$120,550 - $230,400 a yearFull-timeExpandUpdated 2 months ago - UpvoteDownvoteShare Job
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The KYDA Partners team is seeking a Regulatory Affairs Manager to lead and manage the regulatory affairs department, ensuring compliance with regulatory standards and the quality management system.
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The incumbent will perform program analyses to evaluate efficiency and effectiveness of program practices impacting Native American Tribes, legislative and regulatory issues relevant to HHS and IHS.
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In the area of Regulatory Affairs, Biotechnology, or similar field. manufacturing setting with hands‐on experience in quality management systems, or regulatory affairs. perform Regulatory Surveillance of regulatory guidance documents, changes and standards update, and update.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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At least 10+ years of experience in regulatory affairs, with a focus on clinical trials, must be in the pharmaceutical or biotechnology industry. Advanced degree in a relevant scientific or regulatory field (e.g., life sciences, pharmacy, regulatory affairs.
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Support regulatory inspections and Quality responses at company and contract organizations and Represent Regulatory Affairs as SME and process owner in a front? Actively lead and/or contribute to data relevant to Compliance and Regulatory Affairs in periodic Management Review meetings.
$100,000 - $125,000 a yearExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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On experience in quality management systems, or regulatory affairs. Regulatory Affairs / Compliance. Work with operations to conduct gap analyses of standards and regulations such as FDA, EU, ISO, and ICH. Coordinate and prepare responses to requests for information from regulatory agencies.
$100,000 - $125,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. The Quality Control Analyst is responsible for reviewing Medical Disability Examination ("MDE") reports and Disability Benefits Questionnaires ("DBQs") generated by medical providers for veterans evaluated on behalf of the Department of Veterans Affairs (the "VA.
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regulatory affairs jobs in San Antonio, Wells, Nevada
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