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Manufacturing Engineer II
| Company | Medtronic |
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| Location | Ann Arbor, MI, USA |
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| Salary | $81600 – $122400 |
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| Type | Full-Time |
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| Degrees | Bachelor’s |
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| Experience Level | Mid Level |
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Requirements
- Bachelor’s degree with a minimum of 2 years of relevant experience, OR an advanced degree with 0 years of experience.
Responsibilities
- Collaborate with cross-functional team to identify process improvement opportunities.
- Apply appropriate technical skills and tools, such as DOE, SPC, hypothesis testing, capability studies, Gemba walks, and lean manufacturing tools, to perform in depth analysis, determine root cause, and identify corrective actions.
- Identify process improvement opportunities including new fixturing, equipment, and inspection solutions.
- Develops shop floor work instructions and trains operators on equipment and methods.
- Works directly with equipment/machinery suppliers to develop processes, specifications, capability, and suitability for purpose.
- Specifies and purchases equipment and machinery.
- Responsible for the installation of equipment.
- Create test plans and reports to demonstrate technical rationale for associated decisions.
- Execute validation activities (IQ/OQ/PQ) to implement new fixtures and equipment on existing production lines and to poke and yolk and challenge specifications for existing processes.
- Manage project timelines and scope, communicating changes and challenges to key stakeholders.
- Sustain current production through day-to-day support.
- Understand how to flow requirements from a top-level design down to a manufacturing process specification.
Preferred Qualifications
- Exceptional analytical, problem solving & root-cause analysis skills.
- Strong technical aptitude (i.e. able to create, read & comprehend technical drawings and specifications).
- Excellent communication skills (written and oral).
- Team player with demonstrated collaboration track record.
- Medical Device or regulated industry experience.
- Experience managing Quality System Process Documents.
- Experience understanding proper documentation/quality requirements for a regulated environment.
- Experience in selection and/or design of manufacturing equipment, tools and fixtures.
- Experience Process and equipment Validation and Qualification (IQ, OQ, PQ).
- Experience with automation, vision, PLC processes.
- Project management experience.
