• Quality Assurance Engineer

    Danaher Corporation (Muskegon, MI)
    …The Quality Assurance Engineer will be the subject matter expert for the validation strategy and maintain ownership of the Muskegon site Validation Master ... Plan. This position reports to the Quality Assurance Manager and is part of the Quality Assurance Department located in Muskegon, MI and will be an on-site role.… more
    Danaher Corporation (06/27/25)
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  • Sr QC Chemist

    Actalent (Eugene, OR)
    …master's degree or 1 year with a PhD in a QC laboratory within the pharmaceutical , biotechnology, or chemical industry, with at least 3 years in a leadership role. + ... pH meters, + Know how to validate or qualify pharmaceutical test measures (Med device) - test or chemical...radiance (small molecules) + Expedience from large molecules and validation + Tested drug products for API + Experience… more
    Actalent (07/24/25)
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  • Engineer, Engineering - Process (Days)

    Novo Nordisk (Bloomington, IN)
    …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... emphasis on DeltaV, PLC, and HMI technologies. Relationships Reports to Senior Manager , Process Engineering Schedule: regular business hours You will work closely… more
    Novo Nordisk (07/31/25)
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  • Sr Engineer - Electrical

    US Tech Solutions (New Albany, OH)
    **Duration: 12 Month Contract** **Description:** + The Engineer position reports to the Manager of Engineering under the Engineering & Maintenance team at the Client ... non-routine projects involving the planning, design, reconfiguration, construction, maintenance, validation and alteration of systems, facilities and processes. This… more
    US Tech Solutions (07/23/25)
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  • Microbiologist III

    The Ritedose Corporation (Columbia, SC)
    …in-process testing, stability testing, and execution of test method validation when requested. Additional duties include performing environmental monitoring, ... of equipment, laboratory investigations as requested by management, inventory controls, validation assistance, and assisting with the operation of the laboratory as… more
    The Ritedose Corporation (08/02/25)
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  • Scientist I, Analytical Chemistry

    Bristol Myers Squibb (Indianapolis, IN)
    …field + Minimum 5 years of experience in analytical method development, validation , verification, and transfer in the pharmaceutical or radiopharmaceutical ... The person will be responsible for method development and implementation, method validation , verifications, or transfer, as well as stability testing activities to… more
    Bristol Myers Squibb (08/04/25)
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  • QA Specialist I

    Cambrex High Point (Longmont, CO)
    …data and batch production records, Internal/external audits, supplier/subcontractor management, validation , and calibration & maintenance. This role may participate ... and results for accuracy and compliance with other regulatory guidelines. * Under manager supervision, able to comply with GMP, SOPs and basic regulatory guidance. *… more
    Cambrex High Point (08/02/25)
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  • Senior IT Compliance Engineer - FFEx

    Novo Nordisk (Clayton, NC)
    …required + Minimum of four (4) years of experience in computer system validation or quality related discipline experience in pharmaceutical environment required ... 6 weeks paid family medical leave * Free access to Novo Nordisk-marketed pharmaceutical products * Tuition Assistance * Life & Disability Insurance * Employee… more
    Novo Nordisk (07/08/25)
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  • Director, Manufacturing Engineering

    ThermoFisher Scientific (Cincinnati, OH)
    …pharmaceuticals are made with a simplified, end-to-end supply chain for pharmaceutical and biopharmaceutical companies of all sizes. **Position summary** The ... structure to provide direction and management guidance to Capital Engineering, Validation , Utilities, Automation, and Maintenance activities. In addition to leading… more
    ThermoFisher Scientific (05/30/25)
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  • Quality Specialist I

    Element Materials Technology (Santa Fe Springs, CA)
    …approval, and document control. Reports to the Quality Supervisor and/or Quality Manager . $25hr-$35hr DOE **Responsibilities** + Perform QA review of analytical data ... and cGMP. + Participate in QA review of equipment qualification and method validation documentation prepared by technical staff. + Ensure that controlled records are… more
    Element Materials Technology (07/24/25)
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