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Manufacturing Quality Engineer

Grand Rapids, MI 49512

Posted: 08/07/2023 Job Type: Permanent/Direct Hire Industry: Engineering Job Number: 21208 Pay Rate: $ 60000.00 - $ 80000.00

Job Description

Our client in the Greater Grand Rapids, MI area is looking to hire a Manufacturing Quality Engineer for direct hire.  This role requires a highly motivated and results-driven individual with a passion for quality and the ability to work in a fast-paced, deadline-driven environment. If you have a proven track record of success in manufacturing quality engineering and are looking for a challenging and rewarding opportunity, we encourage you to APPLY.

The Manufacturing Quality Engineer is responsible for ensuring that the manufacturing process adheres to quality standards and specifications. This includes implementing and maintaining quality control systems, performing inspections and audits, and identifying and resolving quality issues. The Manufacturing Quality Engineer will work closely with the manufacturing team to improve processes and ensure that products meet customer requirements.

Key Responsibilities:
  • Develop and implement quality control systems and procedures
  • Conduct inspections and audits to ensure compliance with quality standards
  • Identify and resolve quality issues in the manufacturing process
  • Collaborate with the manufacturing team to improve processes and increase efficiency
  • Communicate with customers and suppliers to ensure that products meet their requirements
  • Maintain accurate records and documentation of quality control activities

Job Requirements

  • Bachelor's degree in Engineering, Manufacturing, or a related field
  • Previous medical device manufacturing experience is a plus
  • Experience in quality control and manufacturing operations
  • Knowledge of quality control and inspection techniques
  • Strong problem-solving and analytical skills
  • Excellent communication and interpersonal skills
  • Strong attention to detail and ability to work independently
  • Green Belt or ASQ Certified is a plus
  • Experience with quality management systems (ISO9001, ISO13485 standards and FDA 21) is a plus.
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