Senior Quality Engineer - AS9100 - Lisle, IL
About Our Client
Our client is a manufacturer of electronic components serving both the aerospace and medical device industry. Their product is used in critical devices in both industries, and quality is at the forefront of everything they do. With their developed team, they are looking for a senior level engineer to lead both internal and external projects.
Job Description- Handling day-to-day design, supplier, production, and customer quality issues related to production lines
- Resolving non-conformance's in the production process by identifying the root cause and implementing solutions
- Assist with internal audits to help the company maintain ISO 13485 compliance
- Lead internal IQ/OQ/PQ process
- Assisting with the application and monitoring of established inspection procedures and methods
- Leveraging data findings to implement improvements in the process
- Preparing documentation for customers and suppliers pertaining to quality standards
- Reviewing manufacturing instructions for completeness, correctness, and comprehension by assembly personnel
- Generating standards for suppliers and internal processes
MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
The Successful Applicant- 5+ years of quality engineering experience
- Bachelors degree in engineering or closely related field
- Understanding of Root Cause Analysis problem solving techniques
- Experience with the IQ/OQ/PQ process heavily preferred
- Strong understanding of Lean/Six Sigma methodologies
- Experience in Medical Device, Aerospace, or Automotive industries
- Base salary up to $115,000 depending on experience and interview performance
- 6-7% annual bonus
- Full health benefits
- 3 weeks of PTO
- 11 Holidays
- 401k match
A Manufacturing and Distributor of consumer hand tools in the Northern Chicago Suberbs is looking for a Sr. QualityEngineer to add to their growing team. The company is looking to add new production equipment to their existing...
or an equivalent combination of education and work experience
Minimum 5 years of relevant experience, such as Quality, Compliance, Engineering, within a regulated environment, such as medical device, diagnostics or pharmaceutical industries, to develop...
- Provides solutions to a wide range of problems. Solutions are compliant, innovative, thorough, practical and consistent with organizational objectives.
- Ensures compliant documentation in area of responsibility.
- QualityEngineering...