• Automation Engineer III

    Catalent Pharma Solutions (Chelsea, MA)
    …Engineer III** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... The candidate takes part in ownership of automation engineering, design, and validation . The Automation Engineer III contributes to the design and implementation of… more
    Catalent Pharma Solutions (09/13/25)
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  • Logistics Specialist

    Actalent (Clayton, NC)
    Job Title: Logistics Specialist Job Description A leading global pharmaceutical company is seeking a Logistics Specialist to join their brand new state-of-the-art ... material handling and storage equipment. The Logistics Specialist will ensure the validation of commercial products and oversee the physical handling of materials… more
    Actalent (09/06/25)
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  • Quality Supervisor

    Element Materials Technology (Santa Fe Springs, CA)
    …discipline (advanced degree preferred) + Minimum 5 years of experience in a GMP-regulated pharmaceutical or contract laboratory, with at least 2 years in a ... for overseeing the day-to-day QA operations within a GMP-regulated pharmaceutical environment, ensuring full compliance with applicable regulations, client… more
    Element Materials Technology (08/23/25)
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  • Director, Quality Operations

    Curia (Albuquerque, NM)
    …provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Join our talented workforce, where a commitment ... the Director also supports other quality functions, including QSYS, QC, and Validation , during external engagements. This role is central to maintaining compliance,… more
    Curia (08/23/25)
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  • Director- Solid State

    Astrix Technology (Lafayette, IN)
    …Analytical Chemistry!** Join a cutting-edge team driving innovation in pharmaceutical development and preclinical testing. We're seeking an experienced analytical ... product characterization by solid-state analytical techniques. + Oversee method development, validation , and reproduction of prior art. + Manage workload, staffing,… more
    Astrix Technology (08/16/25)
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  • Application Support Manager - Sap

    Robert Half Technology (Bridgewater, NJ)
    …ability to manage cross-functional support initiatives. Prior experience in the pharmaceutical or biotechnology industry is highly desirable. Key Responsibilities: + ... creation, and troubleshooting. + Experience supporting enterprise applications in a pharmaceutical or biotech environment is highly preferred. + Familiarity with … more
    Robert Half Technology (08/19/25)
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  • Senior Business Systems Analyst/ QA / Jira…

    Motion Recruitment Partners (North Chicago, IL)
    …/ Manual Testing / Waukegan IL North Chicago, Illinois **Hybrid** Contract $55/hr - $60/hr Join a top-tier, mission-driven biopharmaceutical company revolutionizing ... internal analytics with a newly modernized data platform. This is a ** contract opportunity** offering hands-on involvement in both business analysis and QA - ideal… more
    Motion Recruitment Partners (07/18/25)
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  • Sr. Analyst, Managed Care

    Gilead Sciences, Inc. (Foster City, CA)
    …Function as a rebate data subject matter expert to ensure proper data validation , verification of contract compliance, rebate processing, and payment analysis to ... day-to-day administration and processing of all Managed Care Commercial/Medicare Part D contract payments, in support of the contract development activities of… more
    Gilead Sciences, Inc. (08/28/25)
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  • Director, Quality Management - Pharma Repackaging…

    Cardinal Health (Topeka, KS)
    …+ Ensures effective supplier controls for third party suppliers including pharmaceutical and other manufacturers, contract repackagers, and stability ... laboratories + Ensures appropriate quality assurance oversight for contract repackaging facilities + Maintains stability testing program for repackaged… more
    Cardinal Health (09/13/25)
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  • Sr. Director - QC Labs IPM

    Lilly (Indianapolis, IN)
    …methods, and other Quality Control procedures. + To approve and monitor any contract analysts. + To ensure the qualification and maintenance of their department, ... of the manufacturing environment. + Plant hygiene. + Process validation . + Training. + The approval and monitoring of...suppliers of materials. + The approval and monitoring of contract manufacturers and providers of other GMP related outsourced… more
    Lilly (09/03/25)
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