What are the responsibilities and job description for the Senior Quality Engineer position at Intellectt Inc?
Hello,
My name is Jahera, and I’m reaching out from Intellectt Inc. regarding a Senior Quality Engineer contract opportunity in Libertyville, IL(Onsite) with one of our leading clients.
Job Title: Quality Engineer
Company: Intellectt Inc.
Location: Libertyville, IL (Onsite)
Employment Type: Contract (12 Months)
Job Responsibilities
- Set up, operate, and troubleshoot molding processing equipment in a high-volume medical device manufacturing environment.
- Perform quality testing and inspections to ensure products meet specifications and established quality standards.
- Develop and execute Process Failure Mode and Effects Analysis (PFMEA) for molding processes.
- Apply Design of Experiments (DOE) and process characterization techniques to evaluate and optimize manufacturing processes.
- Drive continuous improvement initiatives, root cause analysis, and problem-solving activities to improve product quality and manufacturing efficiency.
- Conduct process test runs, analyze results, and identify production yield issues and opportunities for improvement.
- Prepare quality records, technical reports, charts, and graphs to document process performance and present test results.
- Provide technical assistance to process development and engineering teams for process optimization and manufacturing improvements.
- Ensure compliance with ISO 13485 and applicable medical device quality standards.
- Communicate with customers and internal stakeholders regarding quality issues, process performance, and corrective actions.
Required Qualifications
- Bachelor of Engineering (B.E.) degree or equivalent engineering qualification.
- 5–7 years of experience in quality engineering within a manufacturing environment.
- Hands-on experience with molding processes, preferably injection molding, including equipment setup and operations.
- Strong knowledge of PFMEA, Design of Experiments (DOE), process characterization, and quality testing.
- Experience in high-volume medical device manufacturing.
- Knowledge of ISO 13485 and applicable medical device quality standards.
- Experience with continuous improvement, root cause analysis, problem-solving, and production yield improvement.
- Ability to analyze test results and prepare quality documentation, reports, charts, and graphs.
Pay Scale
- Anticipated hourly pay range: $38-40/hr on W2.
Benefits
Employees hired into this position are eligible for the following benefits, subject to the applicable plan terms and eligibility requirements:
Health Insurance: Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.
Retirement Benefits: A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.
- Paid Time Off (PTO): No PTO other than that required by applicable state and local laws.
Salary : $38 - $40