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Complete audits to assess accuracy and quality of scientific data submitted to the regulatory agencies in support of in vivo medical devices and in vitro diagnostic devices' application. QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.: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.
Full-timeRemoteExpandUpdated 22 days ago - UpvoteDownvoteShare Job
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5+ years of strong investigative or related experience with emphasis on BSA/AML, including writing and preparing SARs in accordance with applicable regulatory requirements. Lead suspicious activity investigations, trade and transaction analysis/research, screening, and regulatory filings (including Suspicious Activity Reports (SARs.
$83,000 - $190,000 a yearFull-timeExpandUpdated 22 days ago - UpvoteDownvoteShare Job
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Regulatory Compliance: Ensure compliance with local, state, and federal regulations related to landscaping, including zoning ordinances, environmental regulations, and building codes. Training and Development: Stay updated on industry trends, best practices, and regulatory changes related to landscaping and share knowledge with the team.
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Familiarity with regulatory requirements and standards, such as FDA, GMP, and ISA. Certification in DeltaV or related control systems. Familiarity with regulatory requirements and standards, such as FDA, GMP, and ISA. Certification in DeltaV or related control systems.
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Appropriate, timely reporting of all matters that are unsafe or unapproved modifications, affect regulatory, ET STCW Rest Hours or living conditions, cable operations, ship navigation, regulatory compliance, monitoring, and/or ISO Process 10 compliance to the Captain, Chief Engineer and/or 40-2121 Department Head as required.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Determine whether all adverse events (AEs) are appropriately reported within the time periods required by GCP, the protocol, the Ethic Committees (IRB/IEC), Sponsor and the applicable regulatory requirement(s.
$55,200 - $96,600 a year depends on experienceFull-timeExpandUpdated 22 days ago - UpvoteDownvoteShare Job
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). Issuing Authority, Series 07 - FINRA, Series 63 - FINRA, Series 65 - FINRA, Series 66 - FINRA.
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The Contract Analyst - Vendor Management will ensure all Third Party relationships are compliant with all applicable corporate, state, federal and regulatory requirements with a focus on Federal consumer financial laws.
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The candidate will develop relationships with key internal and external stakeholders - including regulatory and governing bodies - to ensure that T. Rowe Price's approach to compliance is proactive and preventative.
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Under direct supervision, cleans and services hospital building areas, moves furniture, equipment, and supplies in and around per GBMC, departmental, regulatory agency policies, procedures, and standards.
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Overseeing the administrative, regulatory, and programmatic activities of the Institutional Review Boards (IRB); Institutional Animal Care and Use Committee (IACUC), Institutional Biosafety Committee (IBC), Radiation Safety Committee (RSC), Stem Cell Research Oversight Committee (SCRO), and Laser safety program.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist.
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Maintain regulatory compliance with all governing requirements and licensing agencies (COMAR, MSDE, OSSE); Key Result Area #3: Regulatory Compliance. Work collaboratively with the school's IEP coordinator and student's LEAs to ensure standards of service delivery are aligned with requirements from each jurisdiction served.
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Flexibility to work overtime or other shifts depending on business needs Requirements:Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements.
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You will work directly with all our Pharmaceutical, Biotech, Academic, Govt, and non-profit customers using our gold-standard regulatory, clinical content, cloud-based R&D informatics resources, data science experts and world-class ontologies, and advanced analytics.
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regulatory job in Towson, MD
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