• Director, Patient Services and HUB

    Sumitomo Pharma (Harrisburg, PA)
    …and market access goals. + Collaborate closely with **legal, compliance, privacy and regulatory teams** to ensure program design and execution adheres to all. + ... & Quality:** + Ensure all programs adhere to relevant regulatory and legal standards, including HIPAA. **Qualifications & Skills:**...in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays… more
    Sumitomo Pharma (08/15/25)
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  • Risk & Control Specialist - Independent Risk…

    PNC (Pittsburgh, PA)
    …in the role supporting the Reputational Risk Framework. This includes policy and procedure ownership, committee administration, quarterly risk assessments and ... of the ERM frameworks and ERM Strategy to meet business and regulatory expectations, including performing analysis on the risk framework components. *Support the… more
    PNC (08/15/25)
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  • Senior Director, Complaint Management…

    Olympus Corporation of the Americas (Center Valley, PA)
    …leader will drive cross-functional initiatives to enhance product safety, regulatory compliance, and customer experience through advanced data analytics, digital ... with other functions both within and outside of Quality, including Regulatory Affairs, Information Technology, Service, Repair, Manufacturing, Commercial teams and… more
    Olympus Corporation of the Americas (08/13/25)
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  • RN, Case Manager (Part time), Forbes

    Highmark Health (Monroeville, PA)
    …readmission. + Knowledgeable of and complies with accreditation and regulatory requirements. Integrates performance improvement principles and customer service ... for post-acute services as needed and with compliance with all regulatory and contractual requirements. + Documents, monitors, intervenes/resolves and reports… more
    Highmark Health (08/12/25)
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  • Device Engineer I

    Teva Pharmaceuticals (West Chester, PA)
    …grow through design control practices, physical testing, and documentation to support regulatory filings and product quality. **How you'll spend your day** . Perform ... technical reports, data summaries, and documentation for design verification and regulatory submissions. . Collaborate with cross-functional teams including QA, … more
    Teva Pharmaceuticals (08/09/25)
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  • Communications Governance Manager

    Carrington (Coraopolis, PA)
    …and digital communications. + Conduct regular audits of letter logic and regulatory requirements to ensure accuracy and compliance. + Analyze and streamline ... probing questions to explore alternative solutions and a proper understanding of regulatory and systems alignment. + Collaborate with technology partners to optimize… more
    Carrington (08/09/25)
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  • Coding Auditor Educator

    Highmark Health (Harrisburg, PA)
    …assignments, ICD diagnosis and procedure coding, DRG/APC structure according to regulatory requirements. Reports findings both verbally and in writing and ... materials to address deficiencies identified in the audits compliant with regulatory requirements. Provides written audit guidance. Participates with management in… more
    Highmark Health (08/08/25)
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  • Statutory Accounting Manager, Life and Health

    GE Aerospace (Trevose, PA)
    …the Finance teams and the organization on statutory accounting, filings and regulatory requirements. Assist financial reporting teams as required to ensure all ... filings are completed timely, efficiently and in compliance with state regulatory requirements. + Developing expertise within function. Growing reputation within the… more
    GE Aerospace (08/07/25)
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  • Associate Director of Student Financial Aid…

    Carnegie Mellon University (Pittsburgh, PA)
    …financial aid regulations. This role involves monitoring, interpreting, and disseminating regulatory updates to key stakeholders within the Student Financial Aid ... Director. Furthermore, the Associate Director leads discussions on financial aid policy and independently reviews departmental policies and procedures. They serve as… more
    Carnegie Mellon University (08/07/25)
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  • Senior Director, Global Clinical Development CNS

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    …to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible for all the ... develop the drug in accordance with a clinical and regulatory strategy. + Working with experts and consultants in...PowerPoint, and Outlook). + Knows how/when to apply organizational policy or procedures to a variety of situations. **Physical… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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