• Director - Sterility Assurance

    Lilly (Branchburg, NJ)
    …well as external to Lilly, to ensure strategies are in-line with technical, quality and regulatory guidance, current expectations and business needs. This role also ... develop scientists in the fields of sterility assurance and applied pharmaceutical microbiology + Understanding of cGMP's, policies, procedures, and guidelines… more
    Lilly (08/20/25)
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  • Pharmacy Director

    Arkansas Children's (Little Rock, AR)
    …including strategic planning, fiscal management, human resource management, and quality improvement. Responsible for ensuring compliance with all applicable laws ... and regulatory agencies. Coordinates the provision of optimal pharmaceutical care with available resources. **Additional Information:** **Required Education:**… more
    Arkansas Children's (08/16/25)
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  • Director - Engineering - Formulations…

    Lilly (Indianapolis, IN)
    …needed in the ongoing support of marketed products manufacturing. + Instill a Quality by Design mindset whereby data and learnings from smaller scales and previous ... applicable regulations, and lead the maintenance and improvement of departmental Quality systems. + Establishes effective networks with other engineers within and… more
    Lilly (08/16/25)
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  • Medical Director , Clinical Development…

    AbbVie (North Chicago, IL)
    …and may lead cross-functional teams to generate, deliver, and disseminate high- quality clinical data supporting overall product scientific and business strategy. ... pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. Qualifications Qualifications + Medical Doctor… more
    AbbVie (08/13/25)
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  • Senior Scientific Director , Clinical…

    AbbVie (Irvine, CA)
    …in and may lead cross-functional teams to generate, deliver, and disseminate high- quality data supporting consumer eye care product scientific and business strategy. ... pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. Qualifications *Bachelors degree in the… more
    AbbVie (08/08/25)
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  • Director , Global Strategy

    BioLife Plasma Services (Bannockburn, IL)
    …**About BioLife Plasma Services** BioLife Plasma Services, a subsidiary of Takeda Pharmaceutical Company Ltd., is an industry leader in the collection of high- ... quality plasma that is processed into life-saving plasma-based therapies....United States. Our employees are committed to improving the quality of life for patients and ensuring that the… more
    BioLife Plasma Services (08/02/25)
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  • Scientific Director /Sr. Director

    Lilly (Indianapolis, IN)
    …Collaborate across internal CMC networks (Drug Product Delivery, Project Management, Quality , Manufacturing, and Regulatory) to implement and deliver material and ... phase synthesis, CMC) Additional Skills/Preferences: + Experience within the pharmaceutical sector is preferred. Prior experience in active ingredient development… more
    Lilly (07/22/25)
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  • Associate Director - API SAP EWM

    Lilly (Indianapolis, IN)
    …the SAP EWM design and MES Integration. + Ensure adherence to all quality , compliance and data integrity requirements. + Establish key relationships with business ... and use of SAP, WM and MES integration. + Experience supporting pharmaceutical manufacturing and distribution warehouses with a solid understanding of processes… more
    Lilly (07/09/25)
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  • Director Operational Excellence

    Highmark Health (Montgomery, AL)
    …implements and executes strategies and works with cross-functional clinical, pharmaceutical , operations, IT and performance management improvement teams to ensure ... cause analysis and corrective action, standardization of processes, closed-loop quality management, performance management & continuous improvement, construction of… more
    Highmark Health (09/19/25)
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  • Associate Director , Clinical Operations…

    Takeda Pharmaceuticals (Boston, MA)
    …to ensure the effective execution of the clinical studies on time, with high quality and within agreed budget. **ACCOUNTABILITIES:** + Accountable to the GPT for the ... degree is highly desirable. **Experience:** 10+ years' experience in pharmaceutical industry and/or clinical research organization, including 7+ years clinical… more
    Takeda Pharmaceuticals (09/18/25)
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