• Jt648 - MCS Sr. Manufacturing Associate

    Quality Consulting Group (Thousand Oaks, CA)
    …a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: + Lead and execute CAPAs and EVs related to Biopharmaceutical manufacturing ensuring ... and ensure quality CAPA Applicability responses. + Use project management tools and methodologies to plan, monitor, and report...policies, procedures, and standards, such as cGMP, SOPs, and EHS . + Ensure the right actions have been suggested,… more
    Quality Consulting Group (10/16/25)
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  • Manager, Maintenance- Onsite

    AbbVie (Irvine, CA)
    …day-to-day running of facilities to ensure plant utilities, Facilities and GMP systems are compliant to cGMP and regulatory requirements and meets unique operating ... + Manages the maintenance budget, including external services contracts and spare parts management + Plans business continuity plans in the event of a major failure… more
    AbbVie (09/13/25)
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  • Manufacturing Engineer (Oak Hills, CA)

    3M (Oak Hills, CA)
    …the day-to-day operations, specifically daily tier process, MOC process (change management ), KPI determination, reporting and analysis leading to resolution of any ... tools and methodology (design of experiments, statistical process control, lean management system, kaizens, DMAIC)_ + _Drive process understanding (PPU) efforts and… more
    3M (10/16/25)
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  • Maintenance Supervisor

    Takeda Pharmaceuticals (Van Nuys, CA)
    …of manufacturing equipment and processes + Proficiency with Computerized Maintenance Management Systems (CMMS) and Microsoft Office applications **Important ... with current Good Manufacturing Practices (cGMP), Environmental Health and Safety ( EHS ) guidelines, and all applicable regulations. This role supports the site's… more
    Takeda Pharmaceuticals (08/20/25)
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