• Manufacturing Technician

    Catalent Pharma Solutions (Chelsea, MA)
    …operations for the Good Manufacturing Practices (GMP) production of pharmaceutical products. This individual operates in accordance with environmental, health, ... under direct supervision for the encapsulation and packaging of active pharmaceutical ingredients (APIs). **This is a full-time on-site hourly position. Work… more
    Catalent Pharma Solutions (08/27/25)
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  • Senior Director, Biostatistics

    Amgen (Washington, DC)
    …standards with respect to key variables, variable definitions, statistical methods, data structures and presentation of results; and contributes to statistical ... budgets and resource plans. + Leads and/or participates in the development and review of Policies, SOPs and other controlled documents with CROs or within Amgen's… more
    Amgen (08/24/25)
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  • Sr. Finance Business Partner, AIR

    Chiesi (Cary, NC)
    …care and consumer-facing self-care). We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social ... many other enriching diversities. Chiesi USA Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent… more
    Chiesi (08/22/25)
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  • Pharmacy Supervisor - (Full-time, 1st shift)

    Virtua Health (Voorhees, NJ)
    …Weekly Hours: 40 Additional Locations: Job Information: Job Summary: Provides pharmaceutical care including the dispensing of prescribed medications and other ... of Pharmacy for assigned division of Virtua Health, to provide quality pharmaceutical services in a safe and effective manner. Position Responsibilities Demonstrates… more
    Virtua Health (08/21/25)
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  • Pharmacist Specialist

    UPMC (Altoona, PA)
    …to improve clinical pharmacy services by monitoring processes, analyzing data , implementing interventions, and evaluating the effectiveness of those interventions. ... utilizing therapeutic interchange protocols, and promoting rational drug therapy selection. Review , maintain, and screen patient medication records and profiles for… more
    UPMC (08/20/25)
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  • Director, QA Compliance - Audits & Inspections

    Fujifilm (College Station, TX)
    …Systems. + Excellent written and oral communication skills. + Excellent organizational, analytical, data review and report writing skills. + Ability to set ... for developing, implementing, and maintaining individual sub-systems of the Pharmaceutical Quality Systems (PQS) for FUJIFILM Biotechnologies in TX. Responsibilities… more
    Fujifilm (08/16/25)
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  • Instructor for Master of Science (MS)…

    University of Maryland, Baltimore (Baltimore, MD)
    …(non-tenure track) for the MS in Regulatory Science within the Department of Pharmaceutical Sciences. The MS in Regulatory Science is a two-year master's degree, ... This position is responsible to the Chair of the Department of Pharmaceutical Sciences with teaching responsibility to the Graduate Program Director and Associate… more
    University of Maryland, Baltimore (07/16/25)
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  • Vice President, Business Development, Search…

    Teva Pharmaceuticals (Parsippany, NJ)
    …Lead the initial due diligence process for high-priority opportunities, including data review , competitive landscaping, and risk/benefit analysis. + ... Teva Pharmaceuticals Job Id: 62711 **Who we are** Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving… more
    Teva Pharmaceuticals (07/05/25)
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  • SDD - Advisor

    Lilly (Indianapolis, IN)
    …Additional Skills/Preferences: + Chemical Engineer with strong background in pharmaceutical manufacturing support ( data analysis, modeling, working with ... Lilly, a leading innovation-driven corporation is developing a growing portfolio of pharmaceutical products by applying the latest research from its own worldwide… more
    Lilly (06/17/25)
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  • Principal Scientist, Specialty Testing (LCMS…

    ThermoFisher Scientific (Middleton, WI)
    …multiple projects or programs. + Interact with clients to provide technical project updates, review and evaluate data as needed, and provide input on regulatory ... discipline required 12+ years of relevant experience in a pharmaceutical or analytical testing laboratory that provides the knowledge,...or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and… more
    ThermoFisher Scientific (07/23/25)
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