• Process Engineering Manager

    West Pharmaceutical Services (Williamsport, PA)
    …through our sustainability efforts. **Job Summary** The Process Engineering Manager will lead the engineering team responsible for developing, optimizing, and ... improvement in quality, efficiency, and cost. **Essential Duties and Responsibilities** + Lead and manage a team of process engineers, process engineering… more
    West Pharmaceutical Services (07/18/25)
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  • Sr. Scientist - TS/MS - Dry EM

    Lilly (Indianapolis, IN)
    …life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover ... the reliable and compliant manufacture of the Dry Products External Manufacturing (Dry-EM). The TSMS Representative works with the technical staff responsible… more
    Lilly (09/11/25)
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  • Qualification Engineer

    Teva Pharmaceuticals (Edison, NJ)
    …and local laws, codes, regulations and regulatory requirements + Knowledge of pharmaceutical manufacturing operations to support the approval of protocols, ... **How you'll spend your day** **Essential Duties / Functions** + Lead Site Expansion and Renovation activities, including Commissioning and Qualification for… more
    Teva Pharmaceuticals (07/31/25)
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  • Cleanroom Technician - 1st & 2nd Shift

    Aerotek (San Diego, CA)
    …ensure timely product release and avoid back orders. Work closely with the Team Leader to manage critical raw materials, in-process procedures, and ... to achieve production goals and manage workload peaks. + Coordinate with the Team Leader on raw materials, in-process procedures, and specifications. + Address… more
    Aerotek (09/12/25)
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  • Environmental Monitoring Technician

    Actalent (Maryland Heights, MO)
    …of aseptic processing and controlled area cleanroom environments used for pharmaceutical manufacturing . Conduct quality control or quality assurance activities ... + Proficiency in biology and aseptic techniques. + Exposure to cGMP and pharmaceutical manufacturing . + Experience in lab or regulated environments is strongly… more
    Actalent (09/03/25)
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  • Senior Validation Specialist

    Catalent Pharma Solutions (St. Petersburg, FL)
    …Microsoft Word / PowerPoint / Excel; Minitab; and Scheduling Software. Knowledge of pharmaceutical manufacturing processes and cGMP. + Individual may be required ... Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply… more
    Catalent Pharma Solutions (08/29/25)
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  • Sr Chem Process Engineer

    Mallinckrodt Pharmaceuticals (St. Louis, MO)
    …Time Management ORGANIZATIONAL RELATIONSHIP/SCOPE: Sr. Chemical Process Engineer supports the pharmaceutical manufacturing process and may be assigned within ... Job Description Summary The Sr. Chemical Process Engineer is the recognized technical leader for chemical manufacturing processes and for the improvement of… more
    Mallinckrodt Pharmaceuticals (08/08/25)
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  • Head, Analytical Controls (Sr. Director)

    Takeda Pharmaceuticals (Lexington, MA)
    …is true to the best of my knowledge. **Job Description** **How you will contribute:** + Lead and develop a global team of managers and scientists and their teams ... controls and compliance + Global CMC program oversight of Pharmaceutical Sciences (PS) with management and oversight of all...for people and group management + Inspire confidence in team members and lead the organization culture,… more
    Takeda Pharmaceuticals (09/04/25)
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  • Scientist, Product Development

    Cardinal Health (Indianapolis, IN)
    …validation, as well as occasional testing activities typical for a cGMP pharmaceutical manufacturing operation, including the preparation of chemicals and ... **Job Code:** P39390 - Chem Cnslt, Nuclear Manufacturing **Anticipated salary range:** $79,700 - $113,800 **Bonus eligible:** No **Benefits:** Cardinal Health offers… more
    Cardinal Health (09/04/25)
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  • Sr. IT Engineer 1, CSV

    Fujifilm (Holly Springs, NC)
    …This role provides input and determine action items on all GxP Manufacturing and IT Computerized Systems as well as prepares validation documentation, maintains ... 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging… more
    Fujifilm (08/11/25)
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