• QC Technician (Raw Materials)

    Astrix Technology (Chino, CA)
    …+ Prepare accurate labels, maintain comprehensive documentation, and transfer samples to the Quality Control laboratory . + Apply Good Documentation Practices ... **QC Technician (Raw Materials)** Quality Control Chino, California, US +...sampling procedures in compliance with current Good Manufacturing Practices ( cGMP ), Standard Operating Procedures (SOPs), and relevant FDA regulations… more
    Astrix Technology (01/07/26)
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  • GMP Cell Processing Specialist III

    Actalent (Winston Salem, NC)
    …operations, focusing on cell processing activities while ensuring compliance with cGMP guidelines. This role involves operating and maintaining production equipment, ... mentoring team members, leading investigations, and ensuring high levels of quality and compliance. Responsibilities + Lead and oversee cell processing activities,… more
    Actalent (01/10/26)
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  • Lead Operator, Manufacturing

    ThermoFisher Scientific (Frederick, MD)
    …for operational efficiency. + Partner with adjacent functions to embed robust quality and cGMP practices throughout process changes and continuous-improvement ... cGMP principles, cleanroom regulatory expectations, and end-to-end change control methodologies. + Demonstrated ability to operate autonomously while integrating… more
    ThermoFisher Scientific (12/24/25)
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  • Sr. Conformance Specialist - Berkeley, Ca - Hybrid

    Bayer (Berkeley, CA)
    …assays, specification setting), Supply Chain and Warehouse Management, Validation, and Quality Systems (Deviation and CAPA management, Change Control , Audit ... of current regulatory practices including a current understanding of USP/EP, cGMP regulations, ICH, and FDA Guidance Documents. Provide support during… more
    Bayer (12/04/25)
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  • Operations Associate, Cell Therapy Supply Chain…

    Bristol Myers Squibb (Devens, MA)
    …(COI) **Collaborate & Partner** + Interact effectively with Materials Operations Staff, Quality Control , Quality Assurance and Manufacturing. + Collaborate ... product into cryogenic shipper for shipment to patient **Documentation** + Complete CGMP forms and/or paper/electronic batch records + Perform SAP transactions as… more
    Bristol Myers Squibb (01/12/26)
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  • QC Sample Coordinator I

    PCI Pharma Services (Madison, WI)
    …to work independently as well as on a team, with limited supervisory oversight + Master Control experience a plus + cGMP experience a plus Join us and be part ... QC Sample Management group, which includes use of material control procedures and specification documents, raw material sampling &...needed + Assist with the writing and revision of cGMP documents and Raw Material Specifications documents to meet… more
    PCI Pharma Services (12/09/25)
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  • QA Engineer, - Lilly Medicine Foundry

    Lilly (Indianapolis, IN)
    …(FUME) and computer systems (CSQ) within the Foundry and assures compliance with quality systems and current Good Manufacturing Practices ( cGMP ). This oversight ... includes supporting drug substance manufacturing, central utilities, warehouse, and laboratory facilities. This role is part of a team supporting the design,… more
    Lilly (11/14/25)
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  • QC Technician II - 2nd Shift

    ThermoFisher Scientific (Middletown, VA)
    …The division provides products for drugs of abuse testing, therapeutic drug monitoring, quality control , sepsis diagnosis, prenatal screening and more. How Will ... degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) **Job Description** ** Quality Technician II… more
    ThermoFisher Scientific (01/10/26)
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  • Principal Process Engineer

    Genentech (Hillsboro, OR)
    …partner with experts across Engineering, Process Development, Manufacturing, and Quality to support technology transfer, process optimization, and pioneering ... will be involved with hands-on experimentation in the MSAT process optimization laboratory and will be accountable for providing technical support to the… more
    Genentech (12/19/25)
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  • Pharmaceutical Process Engineer SME

    TAI (Rockville, MD)
    …capacity verification calculations, + Raw material and finished goods format requirements, + Quality control , in-process testing, and Lab strategy, + Product ... CAD designers for the preparation of design drawings. + Performing design quality control . + Collaborating with multidisciplinary teams. + Ensuring compliance… more
    TAI (10/31/25)
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