Quality Engineer I/II - Manufacturing at Applied Medical
RSM, CA 92688, USA -
Full Time


Start Date

Immediate

Expiry Date

03 Aug, 25

Salary

85000.0

Posted On

04 May, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Product Testing, Continuous Improvement, Risk Analysis, Communication Skills, Process Optimization, Technical Documentation

Industry

Mechanical or Industrial Engineering

Description

___________________________:
Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions.
Position Description:
As a Quality Engineer I/II, you will support the company’s Quality System by providing expertise in manufacturing and quality processes. You will offer guidance, training, and suggestions for improvement.

Responsibilities
  • Identifying opportunities for improvement within the Quality Management System (QMS) and implementing systems to enhance process efficiency.
  • Monitor quality metrics and trends and lead the presentation of these insights during management reviews.
  • Create and/or revise process control documentation, such as instructions, control plans, test methods, and graphical aids, as needed.
  • Perform statistical analysis as applicable.
  • Troubleshoot equipment, process and product issues, as needed.
  • Participate in and assess customer complaint investigations, Non-Conformance Reports (NCRs), and supplier control documents.
  • Provide quality engineering support and guidance on inspection methods and equipment, including measurement systems analysis.
  • Contribute to new or updated product and process projects, including risk analysis, master validation plans, product verification and validation, equipment and process validations, and transferring designs to manufacturing as needed.
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