• Quality Operations Specialist I

    Astrix Technology (Irvine, CA)


    Quality Operations Specialist I

     

    Manufacturing

     

    Irvine, CA, US

    Pay Rate Low: 30 | Pay Rate High: 35

    + Added - 05/02/2025

     

    Apply for Job

     

    Our client is a Medical Manufacturing company enhancing vision and improving quality of life through innovative products, partnerships with eye care professionals, and programs that increase access to quality eye care.

     

    Title: Quality Operations Specialist I

     

    Pay: $30-35/hr

    Contract: 12-months **Job Duties:**

    + Review and investigate assigned technical and clinical customer complaints.

    + Perform technical investigations and document results per established procedures and timelines.

    + Supports quality functions pertaining to manufacturing line support and maintenance, including SAP.

    + Performs hands-on troubleshooting of customer returned devices and manufacturing nonconformities and completes associated technical documentation

    + Assist complaint intake group through review and verification of initial complaint coding.

    + Monitor post-market and manufacturing product performance through evaluation and trending of customer complaints, service calls, and manufacturing rejections.

    + Ensure that appropriate corrective actions are implemented to address the root cause of trending issues.

    + Support and coordinate product/process improvements through collaboration with cross-functional teams (Quality, Manufacturing, R&D, Supply Chain, Finance, etc.).

    + Ensure compliance with the company's Quality System policies and procedures and applicable external requirements and standards, including FDA, ISO 13485, and other worldwide regulatory agencies pertaining to medical devices

    Minimum Requirements:

    + Bachelor’s Degree - Engineering/Natural Science/Biomedical/Health Science

    + Years’ Experience: 0-1 years

    + Familiarity with regulatory reporting requirements for medical devices (e.g. MDRs, Vigilance reports, etc.)

    + Familiarity with medical device complaint files and quality records

    + Knowledgeable of FDA regulations, 21 CFR part 820 and Part 803 and ISO 13485 standard

    + Strong computer skills (including Excel)

    + Demonstrated written and verbal communication skills

    INDBH1

    We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.