• Lead Embryologist

    Penn Medicine (Philadelphia, PA)
    …CAP (College of American Pathologists), CLSI (Clinical Laboratory Standards Institute), FDA , FACT, TJC (The Joint Commission), OSHA (Occupational Safety and Health ... in junior roles. + Enters data into computer databases and other software programs meticulously. + Maintains detailed and accurate patient logs and laboratory… more
    Penn Medicine (08/07/25)
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  • Manager, Biostatistics

    Sumitomo Pharma (Harrisburg, PA)
    …Bayesian Statistics + Good understanding and working knowledge of GCPs, ICH guidelines, FDA and other applicable country regulations is a plus + Advanced proficiency ... in BASE SAS and R, or other statistical software is advantageous + Effective verbal and writing skills **Education and Experience** + PhD or MS in statistics or… more
    Sumitomo Pharma (08/02/25)
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  • Customer Care - Product Technical Support…

    ZOLL Medical Corporation (Pittsburgh, PA)
    …that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients ... (https://www.zoll.com/products/supersaturated-oxygen-therapy/therox-sso2-system) Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to… more
    ZOLL Medical Corporation (08/02/25)
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  • Reorder Specialist

    ZOLL Medical Corporation (Pittsburgh, PA)
    …that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients ... (https://www.zoll.com/products/supersaturated-oxygen-therapy/therox-sso2-system) Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to… more
    ZOLL Medical Corporation (08/01/25)
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  • Technician II

    ZOLL Medical Corporation (Pittsburgh, PA)
    …that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients ... (https://www.zoll.com/products/supersaturated-oxygen-therapy/therox-sso2-system) Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to… more
    ZOLL Medical Corporation (08/01/25)
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  • Manager, PVRM

    Sumitomo Pharma (Harrisburg, PA)
    …risk assessment, and safety data analysis + Proficiency with safety databases and software + Ability to evaluate and write case reports and prepare regulatory ... oncology, and/or neurology is strongly preferred. + Comprehensive understanding of FDA and EU legislation and GCP/GVP/ICH safety guidelines for investigational and… more
    Sumitomo Pharma (08/01/25)
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  • Manufacturing Technical Writer--EAM

    Eliassen Group (Harrisburg, PA)
    …actions + Ensure all written materials align with company, quality, and FDA guidelines across all manufacturing components **Experience Requirements:** + Ability to ... + Overall understanding of process instructions + Life Science Experience + Software Skills Required: MS Platform Suite, Oracle, Coupa + Functional knowledge of… more
    Eliassen Group (07/29/25)
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  • Quality Assurance Technician

    ZOLL Medical Corporation (Pittsburgh, PA)
    …that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients ... (https://www.zoll.com/products/supersaturated-oxygen-therapy/therox-sso2-system) Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to… more
    ZOLL Medical Corporation (07/22/25)
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  • Medical Writing Clinical Publisher

    Teva Pharmaceuticals (West Chester, PA)
    …accuracy + Significant editing skills and proficiency in the use of relevant software applications, and using templates and other electronic formats + Advanced Word ... global submissions + Experience with Veeva as EDMS + Knowledge of ICH/ FDA /EU guidelines (clinical documents and publishing) and regulations **Enjoy a more rewarding… more
    Teva Pharmaceuticals (07/22/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    …operations. + Experience with cGMP manufacturing environments and regulatory requirements ( FDA , EMA, ICH). + Familiarity with process validation principles and CPV. ... be considered for employment. We will also not offer you money to buy equipment, software , or for any other purpose during the job application process. If you are… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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