• Bioprocess Analytical Chemist (Purification…

    Eurofins US Network (Andover, MA)
    …of recombinant proteins and other biological therapeutics from early to late stage of development . We are seeking an analytical scientist who will work in a ... believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO...be engaged in the analysis, monitoring and characterization of in- process samples to support the client in improving … more
    Eurofins US Network (01/13/26)
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  • Process Chemistry Intern (PhD)

    AbbVie (North Chicago, IL)
    …the development of new generation AI reactivity models for process critical reactions. Key responsibilities include: + Design and execution of high-throughput ... in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie Interns....for AbbVie Interns. This internship opportunity is in the Process Chemistry group which plays a key role in… more
    AbbVie (01/02/26)
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  • Group Lead, Global Scientific Communications,…

    Takeda Pharmaceuticals (Cambridge, MA)
    …preferably within a matrix structure, in Medical Affairs or Clinical Development (eg clinical scientist , medical information, medical communications, medical ... on programs with complex business deliverables. + Operational experience in pharmaceutical drug development with significant direct exposure to clinical… more
    Takeda Pharmaceuticals (10/23/25)
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  • Small Molecule Process Chemistry Intern…

    AbbVie (North Chicago, IL)
    …world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie Interns. This internship opportunity ... is within Small Molecule Process Chemistry (SM PC) in collaboration with the Center...pre-clinical and clinical space. Under supervision of a Senior Scientist and an engineer, the individual will design and… more
    AbbVie (12/26/25)
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  • Director - Case Management Medical Review

    Lilly (Indianapolis, IN)
    … (eg, epidemiology, toxicology, pharmacovigilance, regulatory affairs). + Experience in the drug development process + Fluent in English, both written and verbal ... around the world. **Purpose:** The Case Management Medical Review Scientist is responsible for conducting comprehensive medical review of...to date up to date on marketed portfolio and development pipeline. + Drive scientific and process more
    Lilly (11/13/25)
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  • Manager, PVRM

    Sumitomo Pharma (Providence, RI)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... of early- to late-stage assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA,… more
    Sumitomo Pharma (10/30/25)
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  • Associate Director, Clinical Sciences, Internal…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …inflammatory disease areas. We are seeking proficient knowledge of the drug development process , Good Clinical Practice, study design, clinical research ... creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements +… more
    Regeneron Pharmaceuticals (01/20/26)
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  • Head of Global Investigative Toxicology

    Sanofi Group (Cambridge, MA)
    …biology, physiology, and pathology. + Solid understanding of the drug discovery and development process based on more than 20 years of experience in ... risk understanding. + Knowledgeable about regulatory nonclinical testing requirements for pharmaceutical development of biologics and small molecules. + Strong… more
    Sanofi Group (11/19/25)
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  • Sr. Study Director - In Vivo

    Charles River Laboratories (Stilwell, KS)
    …with proposal development and management under the supervision of Sr. Scientist /Scientific Manager. * Develop expertise in other areas of speciality, such as ... 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family,… more
    Charles River Laboratories (01/07/26)
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  • 1st Shift Quality Control Laboratory Technician

    Actalent (High Point, NC)
    Description Job Description: The GMP Associate Scientist - is responsible for the complete testing and results documentation of any finished goods, stability and in- ... process samples within the QC Chemistry/Micro Laboratory, in a...ready at all times Up to 5% Training and Development * Participate in ongoing training for the … more
    Actalent (01/17/26)
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