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Sr Quality Engineer Jobs
Company | Medtronic |
Address | Fridley, MN, United States |
Employment type | FULL_TIME |
Salary | |
Category | Medical Equipment Manufacturing |
Expires | 2023-06-13 |
Posted at | 1 year ago |
Careers that Change Lives
Are you passionate about industrial automation and process validation? Are you a project leader who wants to tackle challenging Quality improvements across Medtronic’s Global Operations footprint?
Our Global Quality Strategy is rooted in the Medtronic Mission and our Quality Policy. Being a 'trusted partner' means always putting the patient first, upholding product quality, and maintaining the highest ethical standards in our business relationships and programs. Your dedication to quality is important to our customers and, most importantly, to their patients.
A Day in the Life
As a Sr Quality Engineer, you will be a key member of the Advanced Manufacturing Quality Team and will serve as the process validation SME and Ops Quality representative for Manufacturing Automation system deployment.
You will
• Actively participate in all areas of the equipment development cycle through requirements gathering, risk assessment, specification review, design, and testing
• Be involved in the review and approval of required Equipment and Manufacturing system documents including Development & Validation Plans, Risk Assessments, Requirements Specifications, Design Specifications, Acceptance Test plans and reports, Requirements Traceability Matrices, participating in Design Reviews as required.
• Lead and/or support root cause investigations, drive continuous improvement efforts; collecting, analyzing and interpreting quality performance information and statistical data.
• Contribute to the successful completion of Manufacturing Process Validation initiatives by creating, collaborating, reviewing, and approving documents as required for the Quality Engineering role.
• Interact with cross-functional project team members as well as members of the QA extended team, tracking timelines and facilitating the required Quality Engineering deliverables.
Are you passionate about industrial automation and process validation? Are you a project leader who wants to tackle challenging Quality improvements across Medtronic’s Global Operations footprint?
Our Global Quality Strategy is rooted in the Medtronic Mission and our Quality Policy. Being a 'trusted partner' means always putting the patient first, upholding product quality, and maintaining the highest ethical standards in our business relationships and programs. Your dedication to quality is important to our customers and, most importantly, to their patients.
A Day in the Life
As a Sr Quality Engineer, you will be a key member of the Advanced Manufacturing Quality Team and will serve as the process validation SME and Ops Quality representative for Manufacturing Automation system deployment.
You will
• Actively participate in all areas of the equipment development cycle through requirements gathering, risk assessment, specification review, design, and testing
• Be involved in the review and approval of required Equipment and Manufacturing system documents including Development & Validation Plans, Risk Assessments, Requirements Specifications, Design Specifications, Acceptance Test plans and reports, Requirements Traceability Matrices, participating in Design Reviews as required.
• Lead and/or support root cause investigations, drive continuous improvement efforts; collecting, analyzing and interpreting quality performance information and statistical data.
• Contribute to the successful completion of Manufacturing Process Validation initiatives by creating, collaborating, reviewing, and approving documents as required for the Quality Engineering role.
• Interact with cross-functional project team members as well as members of the QA extended team, tracking timelines and facilitating the required Quality Engineering deliverables.
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