• Program Management Administrator II

    Curia (Albuquerque, NM)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... management, customer service, or related role. + Experience in pharmaceutical /biotechnology industry, strongly preferred Supervisory Responsibilities: This role does… more
    Curia (04/22/25)
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  • Senior Principal Validation Engineer

    Curia (Albuquerque, NM)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... or relevant field + Fifteen (15) years relevant experience in pharmaceutical validation (aseptic/sterile product facility) + Experience with validation tools and… more
    Curia (04/04/25)
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  • Microbiologist III

    Curia (Albuquerque, NM)
    …NM Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Job title is an integral part of ... in a GMP or GLP environment, preferred * Previous experience with pharmaceutical cleanroom environments, preferred * Knowledgeable in FDA cGMPs (21 CFR 211);… more
    Curia (03/30/25)
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  • Director, Quantitative Pharmacology…

    Merck (San Francisco, CA)
    …**Minimum education required:** + Ph.D. with at least seven years of pharmaceutical drug development experience relating to: PKPD, pharmacometrics, mathematics, ... record of increasing responsibility and independence in a similar role in pharmaceutical drug development. **Required Experience:** + Demonstrated impact with… more
    Merck (05/30/25)
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  • Pharmacist

    GAP Solutions Inc (Dublin, GA)
    Position Objective: To provide expert pharmaceutical care by ensuring safe medication dispensing, offering patient counseling, and maintaining compliance with all ... medication orders for appropriateness, compliance or potential abuse; patient's allergy and adverse drug event history; drug - drug and drug -disease state… more
    GAP Solutions Inc (04/17/25)
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  • Senior Principal Scientist, Project Team…

    Boehringer Ingelheim (Ridgefield, CT)
    …and execution of nonclinical safety programs to support the development of drug candidates from discovery to market authorization. The incumbent will be highly ... As the primary interface between global project teams and Nonclinical Drug Safety, the incumbent is responsible for developing nonclinical safety strategies… more
    Boehringer Ingelheim (04/10/25)
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  • Principal Scientist, Pharmacokinetics

    Merck (South San Francisco, CA)
    …DMPK strategy and new capability buildout. **Key Responsibilities:** + Project-team representative and subject matter expert for biologics drug discovery ... is seeking an experienced Principal Scientist to contribute to our biologics, drug conjugates, and novel modality discovery and development pipeline. The ideal… more
    Merck (05/16/25)
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  • Associate Director, Quantitative Pharmacology…

    Merck (Denver, CO)
    …**Minimum education required:** + Ph.D. with approximately 3 years of pharmaceutical drug development experience relating to: PKPD, pharmacometrics, mathematics, ... of increasing responsibility and independence in a similar role in pharmaceutical drug development. **Required Experience:** + Demonstrated impactful experience… more
    Merck (05/30/25)
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  • CDx Associate Director, Global Regulatory Affairs

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... and other devices to enhance the value of our oncology pharmaceutical products. **Responsibilities:** _CDx development_ _:_ Provide critical strategic and tactical… more
    Daiichi Sankyo Inc. (05/29/25)
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  • Sr. Director Quality Operations

    Fujifilm (College Station, TX)
    …meet all CGMP regulatory requirements for phase-appropriate clinical and commercial bulk drug substance and drug product manufacture. **Company Overview** The ... CGMP regulatory requirements for phase-appropriate clinical and commercial bulk drug substance and drug product manufacture. +...& Physical Requirements:_** The physical demands described here are representative of those that must be met by an… more
    Fujifilm (05/08/25)
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