• Surgical Laboratory Technician III

    Charles River Laboratories (Reno, NV)
    …+ Provide anesthesia support to non-surgical studies. + Perform weekly spore validation of autoclave. + Maintain equipment maintenance logs and make arrangements for ... equipment in need of calibration, validation , and/or repair. + Record keeping of Standard Operating...facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our… more
    Charles River Laboratories (07/27/25)
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  • Associate - QA Rep for Dry Product External…

    Lilly (Indianapolis, IN)
    …Manufacturing Quality role provides support to all quality activities at Contract Manufacturing organizations (CMs). The QA Consultant's position is essential for ... support for Quality Control activities + Experience on equipment qualification, system validation and process validation . + Thorough technical understanding of… more
    Lilly (07/24/25)
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  • Senior Associate Scientist, Disc Bioanalytical

    Charles River Laboratories (Mattawan, MI)
    …pharmacokinetic/pharmacodynamic studies. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and ... lead the lab staff in the completion of method validation studies + Provide support to staff members as...facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our… more
    Charles River Laboratories (06/19/25)
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  • QA Associate

    Kelly Services (West Chester, OH)
    …Science & Clinical is seeking a **QA Associate near West Chester, OH.** ** Contract position (~6 months)** **Shift:** 6pm-6am rotating 12 hour shifts (2-2-3 rotating ... QA activities such as batch release, change control, process validation , deviation investigations, SOPs, supplier management, distribution center management, and… more
    Kelly Services (06/18/25)
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  • Logistics Analyst

    Motion Recruitment Partners (New Brunswick, NJ)
    Logistics Analyst New Brunswick, New Jersey **Onsite** Contract $32/hr - $35/hr Our client, a major well known pharmaceutical company is urgently looking to hire ... a **Transportation/Logistics Analyst** to join their team for a long-term contract in **New Brunswick, NJ (ON SITE)** ** Contract Duration: 10 Month contract more
    Motion Recruitment Partners (08/02/25)
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  • QC Microbiologist

    Actalent (La Verne, CA)
    …in a dynamic work environment. Job Type & Location This is a long term contract position with one of the largest pharmaceutical manufacturers in the area. Pay ... and safety of raw materials, in-process and final products, as well as validation -related and critical utility samples. This role is ideal for individuals who are… more
    Actalent (09/14/25)
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  • Sr. Scientist - TS/MS - Dry EM

    Lilly (Indianapolis, IN)
    …Maintain interface with the TS/MS function, development, customers, and contract manufacturing organizations + Manage TS/MS technical projects (experimental, ... as: technical reports, change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, procedures, PFDs,… more
    Lilly (09/11/25)
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  • Pharmacist (Chief Pharmacist)

    Justice, Bureau of Prisons/Federal Prison System (Waymart, PA)
    …all medications are properly packaged and labeled. Responsible for the institution's pharmaceutical budget and ensures national contract compliance as the COTR ... Responsible for all aspects of pharmacy operations including dispensing, pharmaceutical care, clinical and community relations, and accreditation compliance. Plans… more
    Justice, Bureau of Prisons/Federal Prison System (09/11/25)
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  • Senior Scientist I

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …experience in a high-volume pharmaceutical manufacturing QC laboratory or contract pharmaceutical analytical laboratory testing organization is a plus. + ... + Experience in reference standards analysis, including method development and validation . + Proficient with testing involving compendial methods for raw materials… more
    The US Pharmacopeial Convention (USP) (09/09/25)
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  • Microbiologist

    Actalent (Plymouth, MN)
    Microbiologist This is a 12-month contract role requiring a solid understanding of medical device manufacturing in cleanroom environments. While the role is ... based on device and packaging design. + Troubleshoot issues in routine and validation sterilization cycles. + Conduct annual validations for ethylene oxide and steam… more
    Actalent (09/04/25)
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