• Senior Manager, Clinical Partner Outsourcing

    Takeda Pharmaceuticals (Boston, MA)
    …and budget assumptions for complex agreements and develop enhancements to improve validation capabilities + Drive negotiations with CRO's and suppliers to secure ... (eg PMP, CPA) preferred + 7+ years of experience in the pharmaceutical industry or clinical research environment + Experience supporting a complex organization… more
    Takeda Pharmaceuticals (08/08/25)
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  • Research Scientist - Flow / MSD

    ThermoFisher Scientific (Boston, MA)
    …employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. **Key ... and/or external partners in analytical lifecycle activities including method development, validation , cell bank qualification, and method transfer + Be a Subject… more
    ThermoFisher Scientific (08/08/25)
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  • Business Partner (R&D Therapeutic Area Units)

    Takeda Pharmaceuticals (Boston, MA)
    …deriving insights that feed into novel targets identification, target validation and/or biomarker discovery and development. Accountabilities: + **Business ... members and provide suggestions for improvement. **Desired:** + In-depth Pharmaceutical industry and drug development experience. + Professional certification in… more
    Takeda Pharmaceuticals (08/01/25)
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  • Laboratory Equipment IT Engineer, Regeneron Cell…

    Regeneron Pharmaceuticals (Cambridge, MA)
    …with automation systems and control system software + Support engineering and validation projects as well as provide support to manufacturing activities with process ... in a manufacturing/lab/IT setting. Must have experience in a pharmaceutical or biopharmaceutical manufacturing facility. Must have experience with automated… more
    Regeneron Pharmaceuticals (07/26/25)
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  • Senior Director, Precision Medicine Search,…

    Bristol Myers Squibb (Cambridge, MA)
    …degree, eg, MSc, PhD. Specific experience in the diagnostic and pharmaceutical industries, oncology biomarkers, and diagnostic business development. Minimum of 10+ ... years' experience in assay and IVD development including analytical validation , clinical development, manufacturing, US and global regulatory submission, and… more
    Bristol Myers Squibb (07/24/25)
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  • Software Developer

    Takeda Pharmaceuticals (Boston, MA)
    …is at the forefront of digital transformation in the pharmaceutical industry-identifying capability gaps, designing and deploying digital solutions, accelerating ... + Comfortable working with both structured and unstructured data, including data validation and cleaning. + Familiarity with batch ETL pipeline development, SQL, and… more
    Takeda Pharmaceuticals (07/19/25)
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  • Document Control Specialist

    Integra LifeSciences (Braintree, MA)
    …but not limited to, ECRs, DCRs, ECOs, DCOs, and MCOs. deviations, validation records, batch records, and notebooks. + Responsible for processing change orders ... with a working knowledge preferably in the medical device, diagnostics or pharmaceutical industries. Familiarity with FDA regulations and ISO series of quality… more
    Integra LifeSciences (07/16/25)
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  • Winter-Spring 2026 Co-op-Intern-- Recombinant…

    Sanofi Group (Framingham, MA)
    …is responsible for tech transfer activities including process fit-gap assessment, process validation , prepare dossier sections, & PAI support to enable launch of new ... co-op/internship **Preferred Qualifications:** + Experience in a biotechnology or pharmaceutical industry laboratory setting + Experience with downstream processes… more
    Sanofi Group (07/13/25)
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  • Manager, Quality Assurance (QA), Global QMS

    Rhythm Pharmaceuticals (Boston, MA)
    …Veeva QDocs, ensuring documents meet procedural and regulatory requirements. + Participate in validation efforts for new or updated GxP IT systems through review of ... or related field. + 5+ years of relevant experience in the pharmaceutical industry, with established Quality and Compliance knowledge in manufacturing and… more
    Rhythm Pharmaceuticals (07/12/25)
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  • Senior Clinical Research Director, I&I

    Sanofi Group (Cambridge, MA)
    …development activities (eg pressure test and cluster feasibility, medical review and validation of clinical data, study risk assessment) + Contribute to the clinical ... specialist, English fluent (spoken and written) + At least 4 years in pharmaceutical industry or CRO, previous experience in clinical development **Why Choose Us?**… more
    Sanofi Group (07/06/25)
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