• QC Technologist II (C Shift)

    BioFire Diagnostics, LLC. (Salt Lake City, UT)
    …Tuesday 5:45pm-6:15am (3x12) Position Summary QC Technologist II works in a cGMP environment performing quality control testing for commercial and ... departments for data collections and validations for new product QC qualifications, organization of quality controlled materials...II is also responsible for gathering and filling out quality documents pertaining to quality control more
    BioFire Diagnostics, LLC. (09/12/25)
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  • QC Technologist I (C Shift)

    BioFire Diagnostics, LLC. (Salt Lake City, UT)
    …5:45pm to 6:15am (3x12) Position Summary QC Technologist I works in a cGMP environment performing quality control testing for commercial and diagnostics ... work in compliance with company policy and within the guidelines of BioFire Diagnostics' Quality System. + Performs quality control testing on incoming… more
    BioFire Diagnostics, LLC. (09/12/25)
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  • Associate Scientist, QC Sample Management

    Pfizer (Sanford, NC)
    …role, you will: + Perform tasks associated with maintaining Good Manufacturing Practices ( cGMP ) compliant Quality Control and Stability laboratories. + ... accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Quality Assurance and Control more
    Pfizer (10/16/25)
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  • Quality Control Analyst III

    Catalent Pharma Solutions (Chelsea, MA)
    …validation preferred; + Working knowledge of cGMP 's and their application to Quality Control required; + Ability to effectively manage time and prioritize ... ** Quality Control Analyst III** **Position Summary:**...Control Analyst III who is responsible for executing QC testing and related analytical activities supporting product development,… more
    Catalent Pharma Solutions (10/15/25)
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  • Verification Scientist IV

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …for conducting and implementing activities related to current Good Manufacturing Practice ( cGMP ) site audits, quality control and manufacturing (QCM) ... the following responsibilities: + Conducts thorough review and evaluation of QCM [i.e., quality control and manufacturing] documents and other data received from… more
    The US Pharmacopeial Convention (USP) (08/08/25)
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  • Quality Specialist I

    Catalent Pharma Solutions (Manassas, VA)
    …other standard Catalent complies with; responsible for ensuring compliance to FDA and cGMP standards for Quality Control , including continuous training. + ... ** Quality Assurance Specialist I** **Position Summary** Catalent, Inc....or contractors inside the production plant are following our cGMP and execute corrective actions when needed. Assist the… more
    Catalent Pharma Solutions (09/20/25)
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  • Quality Control Analyst II/III…

    System One (Piscataway, NJ)
    …(Master's) + Previous cGMP laboratory experience - required + Strong Quality Control experience in a manufacturing environment + Demonstrated expertise in ... Job Title: Quality Control Analyst II/III Location: Piscataway,...ICH, and FDA standards + Author and revise SOPs, QC methods, technical reports, and investigation summaries + Support… more
    System One (08/19/25)
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  • Quality Control Analyst

    Kelly Services (Louisville, CO)
    ** Quality Control ( QC ) Analyst /...of advanced education and experience will be considered. + Quality Control experience in cGMP regulated ... **Kelly(R) Science & Clinical** is looking for a motivated ** Quality Control ( QC ) Analyst /...science with a minimum of 1 year in a cGMP regulated QC environment. Equivalent combinations of… more
    Kelly Services (10/09/25)
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  • Sr. Associate Scientist - Plate Based

    Actalent (Sanford, NC)
    …Additional Skills & Qualifications + Method validation and transfer experience. + Knowledge of cGMP and quality control processes. + Familiarity with LIMS ... BasedJob Description The Sr. Associate Scientist will support the Quality Control Method Transfer and Validation team...and conducting data analysis. The role requires adherence to cGMP and data integrity principles while reviewing reports and… more
    Actalent (10/07/25)
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  • Scientist Plate Based Assays

    Actalent (Sanford, NC)
    …Qualifications + Assay development + Method validation + Method development + Method transfer + cGMP compliance + Quality control + Familiarity with LIMS + ... Title: Scientist - Plate Based Job Description The Scientist will support the Quality Control Method Transfer and Validation team by performing method validation… more
    Actalent (10/07/25)
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