Quality Engineer
About the role
The Quality Engineer will be based in Buffalo Grove, IL, reporting to Quality Engineer Manager. The Quality Engineer will maintain quality engineering programs, standards and improvements within the organization.
Responsibilities
- Develops and initiates standards and methods for inspection, testing and evaluation.
- Devises sampling procedures and designs and develops forms and instructions for recording, evaluating and reporting quality and reliability data.
- Develops and implements methods and procedures for disposition of discrepant material and devises methods to assess cost.
- Directs workers engaged in measuring and testing product and tabulating data concerning materials, product or process quality and reliability.
- Compiles and writes training material and conducts training sessions on quality control activities.
- Holds up Product Engineers and Quality Program Managers with customer interfaces as necessary on quality related issues.
- Assures data availability and integrity for all quality related data. Consolidates and reports quality results.
- Initiates corrective action requests as needed and tracks to satisfactory completion.
- Assists with development and implementation of quality audits.
- Designs and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and/or production equipment.
- Explores reports and returned products and recommends corrective action.
- Establishes program to evaluate precision and accuracy of production equipment and testing, measurement and research of equipment and facilities.
- Approves product, process and equipment qualifications.
- Provides liaison to various regulatory bodies.
Requirements
- Typically requires a bachelor’s degree in related field or equivalent experience
- 4 years of quality engineer experience
- 3+ years of medical device, Pharma or Biotechnology industry experience
- ISO13485, CAPA, SCARS, NCMR experience
Qualifications
Typically requires a bachelor’s degree in related field or equivalent experience4 years of quality engineer experience3+ years of medical device, Pharma or Biotechnology industry experienceISO13485CAPAS, SCARS, NCMRs experience
Skills
Not specified
Benefits
Not specified
Pay
Not specified
Schedule
Shift: 2:00 pm- 10:30 pm Tue- Sat
Benefits
Not specified
Pay
Not specified
Schedule
Shift: 2:00 pm- 10:30 pm Tue- Sat
Company Information
Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world. A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.
Equal Opportunity Employer
We are an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).