Find Your Next Opportunity
Direct Hire, Contract, Contract to Hire
- Start your job search below
- Filter by Location, Remote Jobs, Keywords, and more. Save your keyword searches for automated notifications when new jobs are added.
- Apply!
iMPact Business Group
https://cdn.haleymarketing.com/templates/62439/images/impact-200x200.png
http://www.impactbusinessgroup.com
http://www.impactbusinessgroup.com
USD
80000.00
95000.00
YEAR
true
Key Responsibilities:
Preferences:
* Six Sigma certification
* Familiarity with APQP (Advanced Product Quality Planning) and PPAP (Production Part Approval Process)
* Experience with electronic medical device manufacturing
Quality Engineer
Grand Rapids, MI 49501 US
Posted: 02/20/2023
2023-02-20
2023-04-22
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
* 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
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
* 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
Preferences:
* 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
* Bilingual in Spanish and English
