• Jt844 - MCS Manufacturing Associate

    Quality Consulting Group (Thousand Oaks, CA)


    QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

    Responsibilities:

    + Perform hands-on operations including equipment setup, cleaning, and sanitization

    + Prepare buffers and media per Manufacturing Procedures (MPs) and SOPs

    + Follow GMP documentation (SOPs, MPs) with strict adherence to safety and compliance

    + Perform and monitor critical processes, including basic troubleshooting

    + Conduct in‑process sampling and operate analytical equipment

    + Execute washroom activities, including cleaning small and large-scale production equipment

    + Maintain an organized and clean workspace

    + Work in a clean‑room environment while wearing steel‑toe shoes, full gowning, hairnet, and gloves

    + Documentation & Quality

    + Initiate quality reports

    + Assist in reviewing documentation such as equipment logs and batch records

    + Identify, recommend, and implement improvements related to routine functions

    + Perform operations in the Manufacturing area, specifically for Purification processes.

    + Operations will be performed according to Standard Operating Procedures (SOPs) while complying with GMP standards in safe manner

    Qualifications:

    + College degree (science-based preferred) Alternatively: Relevant industry or laboratory experience may be considered in place of a degree

    + Experience in biotech, pharmaceutical, or regulated manufacturing environments

    + Science-based background (laboratory, manufacturing, or related field)

    + Familiarity with: SOP adherence, GMP or GLP principles and General laboratory or manufacturing

    + Willing to commit to shift rotations.

    + Schedule: Day Shift or Graveyard Shift (12-hour shifts)

    + Day Shift: 7:00 AM – 8:00 PM or Graveyard Shift: 7:00 PM – 8:00 AM

    Schedule Structure:

    + Front-half and back-half schedules

    + Includes alternating weekends off

    + Initial training will take place on day shift

    + Candidates will transition to assigned shift after training

     

    Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

     

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