• Global Strategic Account Manager

    Danaher Corporation (Cambridge, MA)
    …biotech / genomics industry. + Strong understanding of drug development, manufacturing processes, and regulatory requirements in the pharmaceutical sector. + ... (GSAM), you will be responsible for managing and growing relationships with key pharmaceutical andbiotechnology clients. You will act as the primary point of contact… more
    Danaher Corporation (06/25/25)
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  • Senior Director, Devens Digital Plant and Site IT…

    Bristol Myers Squibb (Devens, MA)
    …operations of the site - to include Commercial and Clinical biologics drug substance manufacturing , site Product Development, and laboratory operations. Member ... and delivery of digital capabilities for Devens Commercial and Clinical Manufacturing , Devens site Product Development (automation), and Laboratory Operations that… more
    Bristol Myers Squibb (08/20/25)
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  • Specialist, Production Scheduler, Cell Therapy

    Bristol Myers Squibb (Devens, MA)
    …+ 3+ years relevant work experience required, preferably in a + regulated pharmaceutical manufacturing environment. + 1+ years of experience supporting ERP ... site plans for operations including apheresis/PBMC receipt, material kitting, process intermediates, manufacturing , and drug product shipments + Point of contact… more
    Bristol Myers Squibb (08/01/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug product at CDMOs + Design and lead ... method validation and implementation activities for drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Commercial Finance Manager (Remote)

    Charles River Laboratories (Wilmington, MA)
    …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... and lead the commercial finance function for our growing Manufacturing Services business unit. This is a newly created...services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their… more
    Charles River Laboratories (08/27/25)
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  • Head, Analytical Controls (Sr. Director)

    Takeda Pharmaceuticals (Lexington, MA)
    …of drug substances and products based on the current Good/Laboratory/ Manufacturing Practice (cGMP, cGLP) regulations + Harmonization and standardization of AD ... 10 years of experience working in CMC analytical development area for active pharmaceutical ingredients and drug products under cGMP's + Demonstrates effective… more
    Takeda Pharmaceuticals (06/06/25)
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  • Head, Discovery, Targeted Therapy

    Astellas Pharma (Cambridge, MA)
    …of therapeutics in Oncology therapeutic area + Deep understanding of pharmaceutical product development, manufacturing , and regulatory science + Contributed ... **Head, Discovery, Targeted Therapy** Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are… more
    Astellas Pharma (06/13/25)
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  • Principal Scientific Advisor

    Charles River Laboratories (Wilmington, MA)
    …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... feel passionate about. **Job Summary** We are seeking an experienced nonclinical drug development professional to serve as a Senior Principal Scientific Advisor… more
    Charles River Laboratories (08/27/25)
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  • Associate Director, Quantitative Pharmacology…

    Merck (Cambridge, MA)
    …record of increasing responsibility and independence in a similar role in pharmaceutical drug development, regulatory agency, or academia. + Educational ... biological constructs, and others. The Associate Director is a skilled quantitative drug developer, with a strong, integrated understanding of the strategic elements… more
    Merck (08/21/25)
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  • Sr. Coordinator, Regulatory Submission Operations

    Cardinal Health (Boston, MA)
    …to the pharmaceutical industry regulatory submissions throughout each phase of drug development and though the drug product life cycle. This individual ... regulatory affairs and product development consulting services to enable pharmaceutical , medical and biotechnology companies to obtain regulatory approvals. More… more
    Cardinal Health (08/13/25)
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