Quality Inspector II

General Atomics

  • San Diego, CA
  • 2 days ago

    Highlights

    Must be customer focused and possess: the ability to read and understand drawings and raw material specifications, and perform basic mathematical computations; the ability to communicate and interface effectively with all levels of employees; the ability to interpret routine information and respond to routine issues; the ability to maintain the confidentiality of sensitive information; and. Under general supervision, this position is responsible for inspecting raw material parts, labels, sub-assemblies, equipment, and finished goods to ensure compliance with company specifications, and quality requirements.

    Numbers & Facts

    LocationSan Diego, CA

    Description

    58538BRQuality InspectorDiazyme PowayCalifornia

    Diazyme laboratories, Inc., is a cGMP and ISO 13485 certified medical device manufacturer (www.diazyme.com). Diazyme uses its proprietary enzyme technologies to develop diagnostic reagents which can be used on most automated chemistry analyzers in user-friendly formats. The products include test kits for diagnosis of cardiovascular disease, liver disease, cancer markers, renal disease, diabetes, and electrolytes.

    We currently have an exciting opportunity for a Quality Inspector located in Poway, CA (San Diego area). This person will join a multidisciplinary Quality team focusing on diagnostic product quality assurance.

    Under general supervision, this position is responsible for inspecting raw material parts, labels, sub-assemblies, equipment, and finished goods to ensure compliance with company specifications, and quality requirements. Sets up, operates, inspects, , parts, subassemblies and finished goods for conformance to specifications. Maintains records, processes, and updates confidential and sensitive electronic and hard copy reports, records and statistics.

    DUTIES AND RESPONSIBILITIES:

    • Inspects raw material parts, components, labels, sub-assemblies and finished goods to ensure compliance with quality specifications using standard operating procedures (SOPs). Maintains quality documentation.
    • May assist with incoming material or equipment testing, as necessary, to verify compliance with requirements.
    • May monitor and verify quality in accordance with statistical process or other control procedures.
    • Works in a lab or warehouse environment requiring long periods of standing, walking, bending and lifting up to 50lbs.
    • Responsible for observing all laws, regulations, and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices.
    • Other duties as assigned or required.

    We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply.

    • Typically requires a high school diploma or equivalent and two or more years of progressive experience in biotechnology, chemical, electrical, mechanical, electromechanical or metrology inspection and calibration.

    • Must be customer focused and possess:

    • the ability to read and understand drawings and raw material specifications, and perform basic mathematical computations;

    • the ability to communicate and interface effectively with all levels of employees;

    • the ability to interpret routine information and respond to routine issues;

    • the ability to maintain the confidentiality of sensitive information; and

    • familiarity with the use of Microsoft office software.

    • The ability to work independently or in a team environment is essential as is the ability to work extended hours as required.

    • Experience with FDA, ISO 9001, ISO 13485, quality assurance program requirements, are desirable.

    QualityEntry-Level (0-2 years) OnsiteFull-Time Hourly 45,00067,1250% - 25% NoNoNo5238091No5313301410.00.027-Oct-2026Quality Inspector II

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