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Quality Engineer

Grand Rapids, MI 49501

Posted: 02/20/2023 Job Type: Permanent/Direct Hire Industry: Engineering Job Number: 21480 Pay Rate: $ 80000.00 - $ 95000.00

Job Description

Are your ready for the opportunity of a life time?  99% of Quality Engineers wish this opportunity was their job.  Our Client, a leader in the Automotive Industry, is seeking an experienced Quality Engineer to join their team. Our client is an energetic yet relaxed company that values work-life balance. They have unique industry processes and automation, and are actively expanding their footprint into the medical industry.

Key Responsibilities:
*    Strong understanding of quality and navigation of the Gray Area (Absolute must have)
*    Driver of customer engagement, very customer centric role
*    Develop, implement, and maintain quality control processes for the Automotive and Medical industry
*    Conduct quality audits and develop corrective action plans
*    Ensure compliance with industry standards and regulations, including ISO 9001 and IATF 16949 for Automotive, and ISO 13485 for Medical
*    Work with cross-functional teams to resolve quality issues and improve processes
*    Collect and analyze data to identify trends and areas for improvement
*    Develop and maintain quality documentation, including procedures, work instructions, and inspection reports
*    Conduct training on quality control processes and procedures
*    Participate in design and process validation activities for new products

Our Client offers a competitive salary and benefits package, as well as opportunities for career growth and development. If you are an experienced Quality Engineer looking for a new challenge in a dynamic and exciting company, we encourage you to apply today.

Job Requirements

*    Bachelor's degree in Mechanical Engineering, Industrial Engineering, or related field
*    5+ years of experience in quality engineering in the Automotive and/or Medical Industry
*    Strong knowledge of quality control processes, including ISO 9001, IATF 16949, and ISO 13485
*    Experience with statistical process control (SPC) and quality tools, such as FMEA, control plans, and root cause analysis
*    Ability to read and interpret engineering drawings and specifications
*    Strong problem-solving skills and attention to detail
*    Excellent communication and interpersonal skills
*    Ability to work independently and as part of a team
*    Proficient in Microsoft Office, including Excel and PowerPoint

*    Six Sigma certification
*    Familiarity with APQP (Advanced Product Quality Planning) and PPAP (Production Part Approval Process)
*    Experience with electronic medical device manufacturing
*    Knowledge of FDA regulations and medical device standards
*    Bilingual in Spanish and English
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