Quality Assurance Inspector I

Argen Corp

  • San Diego, CA
  • 30+ days ago

    Highlights

    This position is responsible for inspecting in-process and finished goods within manufacturing areas to ensure compliance with ISO 13485:2016, FDA regulations, customer specifications, Argen requirements, and applicable procedures. Argen, a global leader in digital dentistry and dental materials, is seeking an HR Generalist to support benefits & LOA administration, HRIS reporting, recruiting, onboarding, and compliance.

    Numbers & Facts

    LocationSan Diego, CA

    Description

    Join Argen as a Quality Assurance Inspector I

    Location: 8515 Miralani Dr, San Diego, CA 92126

    Schedule: Monday-Friday, 7:30am - 4:00pm

    Argen, a global leader in digital dentistry and dental materials, is seeking an HR Generalist to support benefits & LOA administration, HRIS reporting, recruiting, onboarding, and compliance. If you thrive on details, communication, and project management, this role is for you.

    About the Role

    The Quality Assurance Inspector I plays a pivotal role in ensuring the quality and integrity of Argen products. This position is responsible for inspecting in-process and finished goods within manufacturing areas to ensure compliance with ISO 13485:2016, FDA regulations, customer specifications, Argen requirements, and applicable procedures.

    Key Responsibilities

    • Conduct in-process and final inspections and testing as required.
    • Perform visual inspections of finished products.
    • Participate in internal assessments and audits.
    • Maintain accurate inspection and test records.
    • Identify and properly label non-conforming materials.
    • Communicate product/material acceptability to production personnel.
    • Assist with technical problem-solving and special projects.
    • Maintain lot traceability, log sheets, and housekeeping standards.
    • Follow safety policies and regulations to ensure safe work practices.
    • Ensure lab cleanliness and safety standards are upheld.
    • Perform thorough inspections during and after production to ensure quality and compliance.
    • Verify product labeling for accuracy and regulatory compliance.
    • Clear and prepare production lines for subsequent runs.
    • Review and validate Device History Records (DHRs) for completeness and compliance.
    • Perform other duties as assigned.

    What You Bring

    • High school diploma or equivalent required.
    • Experience in a GMP-regulated facility is a plus.
    • Completion of 8 hours of Quality Training (PTC) required.
    • Strong attention to detail.
    • Proficiency in basic arithmetic and problem-solving.
    • Understanding of raw materials, production processes, and quality control.
    • Familiarity with administrative procedures and computer systems.
    • Effective written and verbal communication skills.
    • Ability to interpret technical drawings, artwork, and procedures.
    • Commitment to safety and quality standards.
    • Ability to follow site protocols, policies, and procedures.
    • Flexible, motivated, and capable of working independently.
    • Strong organizational and time-management skills.
    • Problem-solving abilities.
    • Ability to learn technical concepts through documentation and training.
    • Preferred knowledge of regulatory standards including: cGMP, ISO 13485, 21 CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16/2013, MHLW MO 169, TG(MD)R Sch3

    Why You'll Love Working at Argen

    • Competitive pay and full benefits package
    • Medical, dental, and vision insurance
    • 401(k) with employer match
    • Paid time off and wellness programs
    • Employee events and exclusive discounts
    • A collaborative, innovative, growth-focused culture

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