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Manufacturing Engineer III
| Company | Penumbra Inc |
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| Location | Roseville, CA, USA |
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| Salary | $98000 – $137000 |
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| Type | Full-Time |
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| Degrees | Bachelor’s |
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| Experience Level | Mid Level, Senior |
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Requirements
- Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree with 2+ years relevant engineering experience, or an equivalent combination of education and experience
- Excellent written, verbal, and interpersonal communication skills required
- Proficiency in Word, Excel, PowerPoint, Access, and other computer applications required
Responsibilities
- Solve complex problems and implement innovative solutions
- Execute detailed root cause analysis and recommend vetted solutions
- Communicate and explain problems and solutions cross-functionally and interdepartmentally
- Support production; Creating and maintaining product and process documentation; Monitor process and equipment performance and identify and implement process improvement activities to increase/optimize yield, efficiency, and/or throughput
- Design fixtures, acquire off-the-shelf tooling and equipment, and implement new fixturing on the production line
- Test processes, equipment, raw materials, and product. Perform process validations. Author protocols to execute tests, write reports, and make conclusions and/or recommendations based on test results
- Plan, schedule, conduct, and coordinate detailed phases of engineering work as part of a project or as a total project
- Develop specifications of a product, process, or piece of equipment
- Develop, characterize, and optimize processes using statistical techniques and engineering knowledge and experience
- Coordinate with the appropriate suppliers and other external resources needed in developing and implementing process improvement plans
- Participate in project planning and scheduling
- Train assemblers, quality control and technicians, as necessary, on processes, equipment, and documentation
- Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures
- Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company
- Ensure other members of the department follow the QMS, regulations, standards, and procedures
Preferred Qualifications
- Engineering experience in a manufacturing environment recommended
- Medical device industry preferred
- Leadership skills desired
- Knowledge of FDA regulations, Lean/Flow Manufacturing, and/or materials and manufacturing processes desired
