OSI Systems, Inc

  • QA Engineer

    Location US-CA-Hawthorne
    Posted Date 3 months ago(12/12/2018 11:48 AM)
    OSI Electronics, Inc
    Requisition #
  • Overview

    OSI Systems companies have a long history of developing innovative solutions to bring a better quality of life to the world. Healthcare, security and defense are among the key markets where we have made significant inroads with new ideas, products and processes. We know that many people live in difficult and dangerous conditions. To improve these circumstances, experts need simple, effective tools utilizing the latest in technology.


    As a global company, we are dedicated to developing these tools for our customers and the people they serve worldwide. Our singular focus is to help security experts, clinical professionals and high-tech developers solve real-world problems and issues. Our OSI Electronics (OSIE) division is a diversified manufacturer of electronic devices and value-added manufacturing services for use in a broad range of applications, including aerospace and defense electronics, security and inspection systems, and medical monitoring and diagnostics.


    OSI Electronics has a diverse client base that is seeking a Quality Engineer.


    Manufacturing and Customer Quality:

    • Works with a cross functional team (manufacturing engineering, program management, supply chain, production) as well as customers on continuous improvement.
    • Applies Quality Engineering tools and methods such as Six Sigma, lean manufacturing, design of experiments, seven basic quality tools, and Statistical Process Control (SPC).
    • Gather data on customer complaints and production line issues.  Analyzes this data. Recommends and implements improvement.
    • Write and/or respond to defect reports or non-conforming material reports (NCMRs). Disposition material.  Provide instructions for rework or repair.  Work with customers for concurrence when MRB authority is required.
    • Utilizing CATSWEB software, lead CAPA and complaint investigations.  Analyze root cause using 5-Why or similar methodologies.  Implement containment, corrective actions and preventive actions.  Respond to customer using 7-step, 8-D or similar formats.
    • Perform or coordinate with suppliers on failure analysis.
    • Works with manufacturing engineering to generate and execute engineering or document changes. This includes approval of documents and training of personnel.
    • Works with manufacturing engineering to  improve processes.  This includes creating process plans, tooling and validations.
    • Analyze RMAs/ customer returns.  Specify troubleshoot and rework activities for re-shipment.
    • Supports source inspection of product.

    New Product Introduction:

    • Provides knowledge and assistance to the new product development introduction (NPI) process.
    • Ensure compliance with all regulatory requirements, including FDA, MDD, UL, CSA, etc.
    • Write reports and protocols to validate processes using IQ-OQ-PQ methodology.
    • Completes AS9102 FAIRs and Medical Device PPAPs.
    • Coordinate supplier corrective action activities with supply chain and other departments as necessary for supplier quality issues.

    Supplier Quality:

    • Coordinate supplier corrective action activities with supply chain and other departments as necessary for supplier quality issues.


    Quality Systems:

    • Executes the development, implementation, and improvement of the appropriate Quality Management Systems throughout the operation. 
    • May support internal or external audits.


    • Uphold the company’s core values of Integrity, Innovation, Accountability, and Teamwork
    • Demonstrate behavior consistent with the company’s Code of Ethics and Conduct
    • It is the responsibility of every employee to report to their manager or a member of senior management any quality problems or defects in order for corrective action to be implemented and to avoid recurrence of the problem
    • Duties may be modified or assigned at any time to meet the needs of the business.


    • BS degree in: mechanical, electrical, manufacturing, materials, industrial, engineering management or quality engineering OR 2 years of equivalent work experience in electronics manufacturing. Electronic Manufacturing Service (EMS) / Contract Manufacturing (CM) experience preferred.
    • Must be able to demonstrate basic engineering/ applied science knowledge including but not limited to: math, electric circuits, materials, statistics, physics and chemistry.    
    • Knowledge of Six Sigma and/or Lean Manufacturing concepts and tool sets.
    • Knowledge of quality engineering tools, statistical process control (SPC), root cause analysis and containment.
    • Knowledge of ISO9001, AS9100 and ISO13485.


    Equal Opportunity Employer


    EEO is the Law


    Poster Link: http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf



    OSI Systems, Inc. has three operating divisions: (a) Security, providing security and inspection systems, turnkey security screening solutions and related services; (b) Healthcare, providing patient monitoring, diagnostic cardiology and anesthesia systems; and (c) Optoelectronics and Manufacturing, providing specialized electronic components and electronic manufacturing services for original equipment manufacturers with applications in the defense, aerospace, medical and industrial markets, among others.


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