• Labs Data Reviewer…

    ThermoFisher Scientific (Middleton, WI)
    …to accuracy and quality to deliver groundbreaking innovations! **Discover Impactful Work:** The Data Reviewer performs review of a variety of routine ... Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Job Title:** Data Reviewer **Details:** Fully remote, full time **Department:**… more
    ThermoFisher Scientific (12/24/25)
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  • QC Analytical Chemist- Torrance, California

    Prime Matter Labs (Torrance, CA)
    …+ Analyzes compounds to determine chemical and physical properties. + Complete routine review of QC test data and related documents for in-process samples, ... goods and stability samples. + Monitor and trend QC data results + Follows established procedures and documents all...Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits + Assessment of GMP… more
    Prime Matter Labs (11/09/25)
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  • Supplier Quality Manager

    Prime Matter Labs (Torrance, CA)
    …maintain supplier quality assurance programs aligned with FDA, ISO 22716 ( GMP for cosmetics), and other applicable regulations. Conduct supplier audits, assessments, ... Collaborate with cross-functional teams to support continuous improvement initiatives. Develop, Review , Write, and Implement SOP's for quality functions and ensure… more
    Prime Matter Labs (12/16/25)
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  • Principal Engineer, Assay and Data…

    Bristol Myers Squibb (Seattle, WA)
    …a strong technical background in automation design, development, and deployment within both GMP and non- GMP labs . This individual will foster effective ... and experienced Principal Engineer to join the Assay and Data Automation team. This role will lead the design,...automation platforms for bio-analytical methods that are performed in GMP and non- GMP labs . +… more
    Bristol Myers Squibb (12/06/25)
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  • Senior Engineer, Automation

    Merck (Rahway, NJ)
    …capital projects, work to design, install, and qualify new equipment to support GMP clinical production. Write, review or execute test documents. Limited off ... MES, Quality, and Batch Reporting applications. + Understand and adhere to CFR, GMP , and data integrity regulations to ensure compliance with regulatory… more
    Merck (12/05/25)
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  • Engineer, Automation

    Catalent Pharma Solutions (Harmans, MD)
    …from downtown Baltimore. The 200,000 sq. ft. Harmans/BWI-1 facility includes 10 GMP suites, fill/finish operations, testing labs , and warehousing, while the ... on-site** Catalent's Baltimore and Harmans, Maryland sites provide industry-leading GMP development and manufacturing services for advanced biopharmaceuticals, including… more
    Catalent Pharma Solutions (12/12/25)
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  • QA Data Clerk

    Astrix Technology (Gardena, CA)
    **QA Data Clerk** Quality Assurance Gardena, CA, US + Added - 14/05/2025 Apply for Job Our Client, a fine chemical and laboratory products company, is seeking a QA ... Data Clerk to join their growing team. This is...into internal systems. No lab work. **Key Responsibilities:** + Review and process batch records (non-regulated to pharmaceutical-grade materials)… more
    Astrix Technology (10/12/25)
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  • Analytical Technical Steward Peptides…

    Lilly (Indianapolis, IN)
    …control strategies are established for molecules they support. **Responsibilities:** + Technical review , interpretation, and release of data including data ... consistently to predetermined standards. The Analytical Technical Steward reviews data released by contract manufacturers according to API EM...to CM laboratories or to designated third party QC labs . + Monograph review and implementation +… more
    Lilly (11/01/25)
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  • Senior Specialist, Engineering

    Merck (Durham, NC)
    …an Energy Center, Vaccines DP and DS Manufacturing Facilities, Quality Labs , various other manufacturing buildings and Maintenance and Material Storage Facility ... to shutdown schedule including all maintenance, calibration, capital project work, and GMP Cleaning for all facility shutdowns + Coordinates with Site Engineering… more
    Merck (12/19/25)
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  • Quality Assurance Specialist

    Genentech (South San Francisco, CA)
    …activities and documentation such as system risk assessments, decommissioning, and periodic review ; serving as department SME for data migration and archival; ... and related software will be used to support the daily operations and GMP compliance of our state-of-the-art analytical labs and instruments. **Who You… more
    Genentech (11/13/25)
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