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Experience with external beam radiation therapy, brachytherapy, and/or stereotactic radiosurgery+ Strong preference for experience with Varian Truebeam/Aria/Eclipse, CyberKnife and Gamma Knife+ Knowledge of regulatory requirements and accreditation processes in medical physics.
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10) Coordinate project activities with National Park Service, State Park Service, and Client and operational departments such as various park service entities, State Historic Preservation Offices (SHIPO), facilities maintenance, public safety, IT, regulatory affairs, events, and administrators to ensure all parties are well-informed and that work proceeds on schedule with minimal impact.
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Requires national certification from the American Registry of Radiologic Technologists (ARRT), Nuclear Medicine Technology Certification Board (NMTCB), or American Registry for Diagnostic Medical Sonography (ARDMS) based on modalities in which they will be conducting work and licensure by the state regulatory agency as applicable.
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8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer. Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions.
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Deep understanding of AML and KYC counterparty risk identification and mitigation principles, including BSA/AML, CDD/EDD, JMLSG, Sanctions, Fincen CDD, Travel Rule, and TMS global regulatory requirements.
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Certified Internal Auditor or Certified Public Accountant or Certified Regulatory Compliance Manager or Certified Anti-Money Laundering Specialist or Credit Risk Certification (RMA) or Certification in Control Self-Assessment (IIA) or Certification in Risk Management Assurance (IIA) is preferred.
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You perform all functions according to the established policies, procedures, regulatory and accreditation requirements, canine training certification, as well as applicable professional standards.
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With a focus on providing talent for patient support, field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than 30 countries addressing physician and patient needs.
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Firm Type: Law Firm, Experience: 4 Years, A law firm in Phoenix, AZ, is seeking an Energy Regulatory/Corporate Associate Attorney with 4-5 years of experience in energy transactional and regulatory litigation and compliance.
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Using the audit software (Wdesk/Workiva), document process narratives and evaluates the design and operating effectiveness of internal controls to established policies & procedures as well as regulatory guidance.
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Work to ensure that new technology solutions are designed for optimal access and usefulness while meeting SLAs, HIPAA compliance (also other regulatory such as PCI, NIST or HITRUST) and leveraging existing technologies where possibles.
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2 years of experience with relevant regulatory compliance, industry regulations and regulatory data sources such as Office of the Comptroller of the Currency (OCC), Federal Reserve Board, Consumer Financial Protection Bureau (CFPB), etc.
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Previous exposure to corrugated packaging, folding carton, printing, or Point of Purchase (POP) display industries, with a focus on data integrity, quality assurance, or regulatory affairs.
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Land Management Agencies include: Bureau of Indian Affairs, Bureau of Land Management, Bureau of Reclamation, U.S. Fish and Wildlife Service, National Park Service, and U.S. Forest Service. TELEWORK: Indian Affairs has determined that the duties of the position are suitable for telework and the selectee may be allowed to telework with supervisor approval.
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Stay current on industry trends, regulatory changes, and best practices related to healthcare EDI standards and revenue cycle management. Strong communication and interpersonal relationship development with payers both for initial enrollment and for managing changes brought about by regulatory requirements.
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regulatory affairs jobs Title: principal consultant in Laveen, AZ
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