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Quality Engineer

2 months ago

Verona, United States HRL Full time

Job Description:

Our client is seeking a Quality Engineer who will be primarily responsible for resolving and closing, preventative, and corrective actions across all of Smart Manufacturing Accelerator (SMA). Including documented implementation plans and validation audits for preventative and corrective actions, both internal and customer. The Quality Engineer will coordinate the completion of quality system activities to ensure consistent compliance with quality system requirements.



Responsibilities:

Issue and coordinate the completion/close-out of Corrective & Preventive Actions
Evaluates data, prepares graphs/charts, and writes reports to validate or indicate deviations from existing standards.
Closing internal and customer corrective actions (including regional facilities) by monitoring and managing the quality database.
Performs 90 day validation audits.
Develop, implement and improve in-house audit processes.
Developing and maintaining internal audit schedule and validation audit schedule.
Implementing ongoing quality improvement processes working with interdepartmental teams.
Routine quality briefings with production and machining cells.
Writing and reviewing 8Ds, QIRs, and 5 Why documents.
Management of PPAP samples and PPAP filing system.
Preparing and completing action plans in response to corrective and preventative actions.
Reviews quality assurance standards, studies existing policies and procedures, and interviews personnel and customers to evaluate effectiveness of quality assurance program.
Performance of QA studies such as Gage R&Rs.
Management and promotion of SSPs and SSP database.
Ensure compliance with Company Quality Manual and ISO 9001 requirements.



Required Qualifications:

Associates/ Bachelor’s Degree and or equivalent experience in Engineering, Quality or other technical discipline, and three years’ experience. (10+ years’ experience in Engineering, Quality or technical discipline and non-degree w/CQE Certification will be considered lieu of degree)
5 years of experience in a manufacturing/quality environment preferred.
Knowledge of ISO 9001 Quality System Standards, Corrective Action, PPAP, and Discrepant Material management
Working Knowledge (Create & Edit) of MS Office Documents (Word, Excel, Power Point, Access)
Experience utilizing and implementing continuous improvement methodologies and techniques (i.e., Six Sigma, Lean Manufacturing, 5S, Kaizen).