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Deliver professional cross-divisional/cross-functional Global Security (GS) investigations throughout the United States, representing the vanguard of Novartis’s Corporate Governance response to internal fraud, healthcare compliance, corruption and other alleged internal misconduct, including violation of company policies, improper conduct and regulatory violations involving employees, customers and/or affiliates.
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About the Opportunity This is an open position with FirstEnergy Service Co., a subsidiary of FirstEnergy Corp. [SC00] ACCOUNTABILITY OBJECTIVE As part of the Voice & Video Operation team, responsible for architecture, engineering, design, implementation, operation, maintenance, regulatory compliance, and ongoing reliability for Voice & Video computing devices such as application servers, IP PBX/Telephones, and audio & video conferencing systems.
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Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion diagnostic tests, digital health and other devices to enhance the value of our pharmaceutical products across therapeutic areas.
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Ensure Equipment Compliance: Receive and review revisions to USP, EP, JP, FDA regulatory guidelines. The incumbent in this individual contributor role ensures the compliance of equipment and the ECQ group with local, global, and regulatory guidelines.
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Provide oversight to assure that all validation work performed for Daiichi Sankyo by various contractors meets Global DX Computer System Validation requirements, global regulatory compliance, and global Quality expectations.
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Must have completed most of the requirements towards earning the ABA Certified Regulatory Compliance Manager (CRCM) certification). Participate in regulatory compliance examinations performed by the OCC and CFPB. Documents results and presents to management.
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Proven experience collaborating with financial partners to ensure regulatory compliance across various domains including financial crimes, money movement, product obligations, and consumer compliance.
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Ensure that all activities and duties are carried out in full compliance with regulatory requirements, Enterprise Wide Risk Management Framework and internal Policies and Policy Standards.
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Job Title: Compliance Specialist Duration: 12 Month Contract (Possible extension based on work performance) Location: Summit, NJ Hybrid Position JOB DESCRIPTION: Purpose and Scope of the Position The Compliance Specialist, Equipment Commissioning & Qualification, supports the successful operation of facility, laboratory, and business functions at multi‐use sites through interaction with internal team members and peer‐level customers as well as external service providers.
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Regulatory compliance of Payment cards processing in USA like Reg-Z, SOX, PCI-DSS etc. Should have experience in Mainframe Application Development along with strong hands-on Cobol, JCL, VSAM, Db2 and Mainframe Utilities CICS.
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Under the direction of Regulatory Affairs management, participate in drug development from early stage development through final formulation, ensuring compliance with principles of Quality-by-Design, cGMP, and FDA rules and regulations.
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The Quality Assurance Coordinator reports to the Laboratory Quality Assurance Manager or Quality Specialist and is responsible for supporting the overall quality assurance program by assisting in essential functions and tasks to ensure compliance with all relevant regulatory and company standards while ensuring traceable and defensible data.
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Receive and review revisions to USP, EP, JP, FDA regulatory guidelines. Job Description: minimum % onsite Purpose and Scope of the Position The Compliance Specialist, Equipment Commissioning & Qualification, supports the successful operation of facility, laboratory, and business functions at multi-use sites through interaction with internal team members and peer-level customers as well as external service providers.
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Familiarity with financial regulatory compliance and anti-money laundering (AML) processes. Familiarity with financial regulatory compliance and anti-money laundering (AML) processes. As an Oracle/Mantas Developer, your primary responsibility will be the development and maintenance of in-house products using Oracle/Mantas, specifically focusing on transaction monitoring tools.
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Job Responsibilities Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting.
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regulatory compliance jobs in Morris Plains, NJ
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