OSI Systems, Inc

  • Quality Engineer III

    Location US-CA-Hawthorne
    Posted Date 2 weeks ago(6/1/2018 5:18 PM)
    Company
    OSI Electronics, Inc
    Requisition #
    14137
  • Overview

    OSI Systems companies have a long history of developing innovative solutions to bring a better quality of life to the world. With more than 30 years of combined experience in the field of optoelectronics our OSI Optoelectronics (OSIO) division is a diversified manufacturer of standard and custom photodiodes and optical sensors for used in aerospace, defense, commercial and medical applications.

     

    We are one of the largest global manufacturers of optoelectronic devices, delivering engineering design support and manufacturing capabilities that include products for use in the defense, aerospace, medical, and industrial markets, among others. We utilize our world-class manufacturing facilities in the U.S., India and Malaysia to continue to put forth excellent engineering solutions aligned with efficient manufacturing to meet high-volume production requirements.

     

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

    Responsibilities

    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.

    General

    • Maintain the integrity and quality of our products to our customers.
    • Insure that safe operating procedures are developed, communicated, and followed by all personnel.
    • Uphold the company’s core values of Integrity, Innovation, Accountability, and Teamwork
    • Demonstrate behavior consistent with the company’s Code of Ethics and Conduct

    Qualifications

    • BS degree in: mechanical, electrical, manufacturing, materials, industrial, engineering management or quality engineering
    • 5+ years of 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, customer complaints and containment.
    • Knowledge of ISO9001, AS9100 and ISO13485.

    *This position is expected to be exposed to information which is subject to US export control regulations, i.e. the International Traffic in Arms Regulations (ITAR) or the Export Administration Regulations (EAR).  All applicants must be U.S. persons within the meaning of U.S. regulations. 

     

     

    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.

     

     

     

    Options

    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed

    Connect With Us!

    Not ready to apply? Connect with us for general consideration.