• Director / Sr. Director - mRNA Process Development

    Lilly (Indianapolis, IN)
    …manufacturing partners. + Collaborate with cross-functional teams (eg Research, Analytical, Drug Product, Clinical and Regulatory ) to align process development ... Deep purification and engineering background + Familiarity with LNP formulation and drug product considerations. + Strong regulatory interaction experience (FDA,… more
    Lilly (10/14/25)
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  • Head of Solid Tumors, Global Medical Affairs…

    AbbVie (Mettawa, IL)
    …oncology solid tumor portfolio. This role requires expertise in oncology drug development, clinical trials, regulatory interactions, and cross-functional ... goals. The role will involve close collaboration with clinical development, commercial, regulatory affairs, and market access teams to ensure alignment of the… more
    AbbVie (12/09/25)
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  • Supplier Quality Manager

    Permobil (Lebanon, TN)
    …trained to audit: Regulatory requirement CFR 820 issued by Food and Drug Administration in USA. Regulatory requirement EU Regulation 2017/745 issued by the ... SQM aligns supplier capabilities with Permobil's design, quality, and regulatory requirements, and ensures robust compliance with the Quality Management… more
    Permobil (12/09/25)
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  • Therapeutic Strategy VP,…

    IQVIA (Washington, DC)
    …and identifying new business opportunities. + Provide due diligence scientific, medical, regulatory , and drug development expertise and activities for IQVIA or ... impact in the field. A strong background in current FDA regulatory expectations and the global landscape in Cardiovascular/Metabolic/Renal/Respiratory is preferred.… more
    IQVIA (12/12/25)
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  • Patient Access Representative, Lead Registrar, Bed…

    Stony Brook University (Stony Brook, NY)
    …a minimum of three (3) professional references. + Successfully complete a 4 panel drug screen * + Meet Regulatory Requirements for pre employment screenings. + ... prescribed workflows. Responsible for completing inpatient registration and securing regulatory documents/signatures. Responsible for coordination between physicians, patient units… more
    Stony Brook University (12/02/25)
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  • Shift Supervisor Blood Bank - Day Shift

    Stony Brook University (Stony Brook, NY)
    …a minimum of three (3) professional references. + Successfully complete a 4 panel drug screen * + Meet Regulatory Requirements for pre employment screenings. + ... System_ WellSky Transfusion to conform to the changing operational and regulatory requirements of the department. Inclusive of database changes, test development… more
    Stony Brook University (11/26/25)
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  • Clinical Lab Technologist II -Blood Gas Technician

    Stony Brook University (Stony Brook, NY)
    …a minimum of three (3) professional references. + Successfully complete a 4 panel drug screen * + Meet Regulatory Requirements for pre employment screenings. + ... II. * Communicate effectively with Main Laboratory, Point of Care Dept., regulatory agencies and vendor technicians * Assist in teaching respiratory therapists,… more
    Stony Brook University (11/22/25)
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  • Patient Access Representative - Offsite Outpatient…

    Stony Brook University (Stony Brook, NY)
    …a minimum of three (3) professional references. + Successfully complete a 4 panel drug screen * + Meet Regulatory Requirements for pre employment screenings. + ... Offsite Hospital Outpatient Registrar reviews registrations for completeness, obtains regulatory consents, and ensures financial clearance is complete, collecting… more
    Stony Brook University (11/15/25)
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  • Clinical Trial Mid-Level Project Manager

    Vitalief (Washington, DC)
    …to leadership as needed. + Oversee study documentation, including case report forms, drug records, and regulatory filings. + Motivate team members and ... ensuring trials are executed efficiently, on budget, and in compliance with regulatory standards. The Project Manager bridges scientific and operational aspects of… more
    Vitalief (10/31/25)
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  • Pathologist Assistant, Anatomic Pathology Support…

    Stony Brook University (Stony Brook, NY)
    …a minimum of three (3) professional references. + Successfully complete a 4-panel drug screen * + Meet Regulatory Requirements for pre-employment screenings. + ... who will maintain & develop Grossing/Autopsy policies and procedures in accordance with regulatory agencies ( ie CAP, NYSDOH, etc.) and prepare Grossing Room for… more
    Stony Brook University (10/08/25)
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