Senior Quality Engineer
Intellectt Inc · North Haven, Connecticut, United States
FULL TIMEpermanent
Job Description
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.
For a complete understanding of this opportunity, and what will be required to be a successful applicant, read on.
Job Title: Quality EngineerCompany: Intellectt Inc.Location: Libertyville, IL (Onsite)Employment Type: Contract (12 Months)
Job ResponsibilitiesSet 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 QualificationsBachelor 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 ScaleAnticipated hourly pay range: $38-40/hr on W2.
BenefitsEmployees 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. xzbcwsv Paid Time Off (PTO): No PTO other than that required by applicable state and local laws.
For a complete understanding of this opportunity, and what will be required to be a successful applicant, read on.
Job Title: Quality EngineerCompany: Intellectt Inc.Location: Libertyville, IL (Onsite)Employment Type: Contract (12 Months)
Job ResponsibilitiesSet 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 QualificationsBachelor 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 ScaleAnticipated hourly pay range: $38-40/hr on W2.
BenefitsEmployees 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. xzbcwsv Paid Time Off (PTO): No PTO other than that required by applicable state and local laws.
Details
| Company | Intellectt Inc |
| Location | North Haven, Connecticut, United States |
| Type | FULL TIME |
| Niche | tech |
| Experience | permanent |