Previous Job
Senior Supplier Quality Engineer
Ref No.: 18-50763
Location: Jacksonville, Florida
Start Date / End Date: 09/17/2018 to 09/13/2019
Company: Artech Information Systems
Job Title: Senior Supplier Quality Engineer
Location: Jacksonville, FL
Duration: 12+ months
Job Id: - 18-50763
This position has the responsibility and authority to provide Quality Assurance Engineering representation to select business teams facilitating front-end design, design transfer to manufacturing, and process improvements to obtain optimum product reliability, safety, and effectiveness. Coordinate feedback of quality indicators and statistics to business team for use in business decisions. Partner with Manufacturing Engineers in process improvements. Perform, direct, or consult in validations. QA approvals for Engineering Change Notices, test methods, and test equipment to assure the design and production of medical devices are in compliance with applicable standards. Drive investigations, corrective action implementation, and corrective action verification activities assigned to business teams.
  • Partners with Manufacturing Engineering to assist in developing test methods, equipment acquisition for new product testing, validations/qualifications, statistical analysis of data for significance, and other documented requirements for quality objectives.
  • Participates in new product development to select suppliers, qualify new suppliers, and setup supplier controls.
  • Investigates and reports on supplier corrective actions effectiveness and timeliness.
  • Participate on Corporate Supplier Quality Teams.
  • Develop and ensure proper execution of the Supplier Quality Strategy.
  • Manage all Jacksonville Supplier Quality activities.
  • Partner with Supply Chain to integrate strategies and ensure coordination and alignment across Sector.
  • All activities must be performed in compliance with the Quality System.
  • Performs duties in compliance with environmental, health and safety related site rules, policies or governmental regulations.
  • All other duties as assigned.
  • Travel requirement: less than 25%
  • Bachelor's degree or Master's degree preferably in mechanical engineering
  • Three or more year’s experience with a BS degree or three or more year’s experience with a Master's degree.
  • Minimum of three years industry experience, preferably in the medical device manufacturing.
  • Experience in medical device process validation and test method validation
  • Experience in application statistical methods to design reliability and process capability.
  • Experience in machining and molding manufacturing processes
  • Strong oral and written communication skills.
  • Cross-functionally and an effective team player.
  • Excellent presentation skills.
  • Must be able to handle multiple tasks/projects and manage priorities accordingly.
  • Working knowledge of appropriate industry standards.
  • Experience in application statistical methods to design reliability and process capability.
  • Must be able to work in a team environment and exert influence without alienating others.
Rajiv Maruthi