• Manager, QC Biochemistry, Hopewell Site

    BeOne Medicines (Pennington, NJ)
    …laboratory through late phase activities. + Oversee QC Biochemistry laboratory related quality systems to ensure conformance with regulations and BeOne Global ... quality standards. + Supervise a highly efficient QC Biochemistry...2 years managing laboratory analysts in an FDA-regulated biotechnology, pharmaceutical company with progressive levels of responsibility are required.… more
    BeOne Medicines (09/19/25)
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  • Lead Process Engineer Liquid

    ManpowerGroup (Wilson, NC)
    …you will play a critical role in ensuring the efficient, safe, and high- quality manufacturing of liquid and oral solid dosage (OSD) consumer health products. This ... OSD processes to improve efficiency, reduce waste, and ensure product quality . + Provide technical support, troubleshooting, and corrective action implementation. +… more
    ManpowerGroup (09/19/25)
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  • QC Chemist

    Astrix Technology (Albany, NY)
    **QC Chemist** Quality Control Albany, NY, US Pay Rate Low: 35.00 | Pay Rate High: 44.00 + Added - 08/09/2025 Apply for Job Astrix is proud to partner with a ... recognized contract research, development, and manufacturing organization (CDMO) serving the pharmaceutical and biotech industries. We are seeking a motivated and… more
    Astrix Technology (09/12/25)
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  • Pharmacy Operations Manager

    BrightSpring Health Services (Irving, TX)
    …to market, and an industry shift from hospital delivery settings to lower-cost, high- quality alternative providers such as Amerita. As a core member of the Pharmacy ... the advisement of the General Manager. This will include: Oversees multiple pharmaceutical services including pharmaceutical care activities for customers within… more
    BrightSpring Health Services (09/12/25)
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  • CMC Project Lead, Synthetics

    Sanofi Group (Framingham, MA)
    …CMC team with representatives from CMC Development, Manufacturing and Supply, Quality , Dossiers, Regulatory, Demand and Supply, + He/she creates with the ... ensures that the project development follows actual standards and define the Quality Target Product Profile (QTPP) and product development targets. He/she is… more
    Sanofi Group (09/09/25)
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  • cGMP Associate Director, Process Development

    University of Southern California (Los Angeles, CA)
    …in order to ensure that project deliverables meet schedule, cost, scope, quality , and safety and ensuring continuous improvement by engaging all employees. Job ... for product testing. + Lead technology transfer to cGMP manufacturing and quality control, ensuring efficient scaling and implementation. Develop and review SOPs,… more
    University of Southern California (09/08/25)
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  • Clinical Pharmacist Specialist-Internal Medicine

    UPMC (Harrisburg, PA)
    …preventing medication adverse events. Additionally, they conduct research, support quality initiatives, and provide education and training. **Responsibilities:** + ... service lines, clinical areas, and therapeutic programs + Facilitates pharmaceutical care services, direct patient care programs, medication utilization systems… more
    UPMC (08/26/25)
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  • Sr Pharmacy Clinical Specialist - Full Time - Days…

    Houston Methodist (Houston, TX)
    …to fulfilling the organization's mission to provide innovative, personalized, cost-effective pharmaceutical care in a culture dedicated to quality and ... documents patient care activities and patient outcomes as impacted by pharmaceutical care and clinical interventions. + Provides patient-specific and non-patient… more
    Houston Methodist (08/19/25)
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  • Director, Hospital Pharmacy - Pharmacy - Full Time

    Guthrie (Sayre, PA)
    …This role involves ensuring the safe, effective, and efficient delivery of pharmaceutical care to patients while complying with all applicable regulations and ... collaboratively with healthcare professionals to optimize patient outcomes and enhance the quality of care provided. Education, License & Cert: Doctor of Pharmacy… more
    Guthrie (08/13/25)
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  • Sr. Director Research - Administration - Full Time

    Guthrie (Sayre, PA)
    …in STEM discipline). + Minimum 3-5 years of direct experience in clinical or pharmaceutical -sponsored research or regulatory fields such as the FDA, NIH, or HHS. + ... implementing rigorous oversight of human subject protocols, training programs, and IRB quality assurance processes. Assures that the IRB has appropriate resources to… more
    Guthrie (08/13/25)
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