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It can be valuable for candidates involved in the development and submission of IVD products to regulatory agencies like the FDA.Regulatory Affairs Certification (RAC): A certification in regulatory affairs, such as the RAC from the Regulatory Affairs Professionals Society (RAPS), can be beneficial for candidates involved in FDA IVD application processes.
$118,000 - $147,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Director, CMC Regulatory Affairs. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
$100 - $113 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Develop and implement Data Loss Prevention (DLP) policies specifically for Fabric and Power Platform connectors to safeguard sensitive data and ensure compliance with legal and regulatory standards.
$70 - $90Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Stay informed of changes in regulatory requirements, industry trends, and emerging threats related to BSA/AML compliance, providing guidance and recommendations to internal stakeholders. Preferred Qualifications- Proven track record in developing and implementing compliance programs for financial institutions, with a focus on BSA/AML requirements and regulatory obligations.
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Reporting to the Clinical Research Manager of Blood & Marrow Transplantation and Cell Therapy (BMT-CT), the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to to manage data, enroll and follow patients on trial, and assist with regulatory and financial requirements of the trials.
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This position is part of Clinical Affairs team and will be hybrid to Sunnyvale, CA. The senior clinical research scientist will work on advanced, complex projects requiring state of the art knowledge in oncology and/or infectious disease molecular diagnostics.
$103,000 - $142,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Ability to create and maintain regulatory labels using CorelDraw or equivalent. Participate in in-house or outside testing for agency compliance of F5 product(s) for safety, EMI/EMC, NEBS, and other regulatory standards.
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Provide input into the design of statewide conservation policy strategies with the Director of California Policy and Government Affairs and other members of the U.S. and California Ocean Conservation Team.
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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 Today - UpvoteDownvoteShare Job
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Participate in community affairs and maintain positive public image for HHM and hotel. Area General Manager – Regional Director of Operations – Vice President of Operations. Area General Manager – Regional Director of Operations – Vice President of Operations.
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Support Danaher Diagnostic Operating Company Medical and Scientific Affairs and Government Affairs organizations on their strategy so that it maximizes patient impact at scale. Prior roles in industry Medical and Scientific Affairs and/or Government Affairs functions a plus.
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The Senior Manager/Director of Policy and Regulatory Affairs will play a pivotal role in shaping and advancing our client's strategic initiatives across PJM and regulatory landscapes.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
$1,595 a weekFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Foundation for Hispanic Education (TFHE) seeks a Director of Finance, who will be responsible for managing the financial and business affairs of TFHE. Reporting to the Chief. Executive Officer, the Director of Finance will be a highly-analytical director, overseeing our organization's financial planning and accounting operations.
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Plan, develop, and execute relevant bench-top, pre-clinical and cadaver studies as needed for regulatory, clinical and R&D requirements. Develop and execute processes in alignment with all regulatory and quality standards.
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regulatory affairs jobs Title: sr director Company: Planet Pharma in Santa Clara, CA
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