Electrical Manufacturing Engineer III - Medical Device
Job in
San Francisco, San Francisco County, California, 94199, USA
Listed on 2025-12-11
Listing for:
Penumbra, Inc.
Full Time
position Listed on 2025-12-11
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering, Process Engineer
Job Description & How to Apply Below
Electrical Manufacturing Engineer III - Medical Device
Base pay range: $/yr - $/yr
Responsibilities- Solving complex problems and implementing innovative solutions.
- Executing detailed root cause analysis and recommending vetted solutions.
- Communicating and explaining problems and solutions cross‑functionally and interdepartmentally.
- Collaborating closely with suppliers, ensuring timely communication of updates and respectfully requesting any necessary changes.
- Engaging in troubleshooting of electromechanical products using failure analysis and problem‑solving techniques, while recommending and implementing effective solutions.
- Leading the implementation of projects at the supplier level, managing communications related to test plans, monitoring project timelines, and ensuring all milestones are met efficiently.
- Approaching problems from a detail‑oriented perspective.
- Suggesting independent recommendations for project approach, scope, and tactics.
- Supporting production: creating and maintaining product and process documentation; monitoring process and equipment performance and identifying and implementing process improvement activities to increase/optimize yield, efficiency, and/or throughput.
- Designing fixtures, acquiring off‑the‑shelf tooling and equipment, and implementing new fixturing on the production line; performing equipment qualifications.
- Testing processes, equipment, raw materials, and product; performing process validations; authoring protocols to execute tests, writing reports, and making conclusions and/or recommendations based on test results.
- Planning, scheduling, conducting, and coordinating detailed phases of engineering work as part of a project or as a total project.
- Developing specifications of a product, process, or piece of equipment.
- Developing, characterizing, and optimizing processes using statistical techniques and engineering knowledge and experience.
- Coordinating with the appropriate suppliers and other external resources needed in developing and implementing process improvement plans.
- Participating in project planning and scheduling.
- Training assemblers, quality control and technicians, as necessary, on processes, equipment, and documentation.
- Performing other activities requiring knowledge of principles and techniques commonly employed in the specific area of projects.
- Adhering to the company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures.
- Understanding relevant security, privacy and compliance principles and adhering to the regulations, standards, and procedures that are applicable to the company.
- Ensuring other members of the department follow the QMS, regulations, standards, and procedures.
- Performing other work‑related duties as assigned.
- Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or a related field with 2+ years relevant engineering experience, or an equivalent combination of education and experience.
- Engineering experience in a manufacturing environment recommended; medical device industry preferred.
- Experience with electronic devices and/or PCBA.
- Experience with contract manufactured electromechanical medical device products.
- Excellent written, verbal, and interpersonal communication skills required; leadership skills desired.
- Knowledge of FDA regulations, Lean/Flow Manufacturing, and/or materials and manufacturing processes desired.
- Proficiency in Word, Excel, PowerPoint, Access, and other computer applications required.
Alameda, CA
Annual base salary: $109,000 to $152,000
Working Conditions- General office, laboratory, and clean room environments.
- Willingness and ability to work on site.
- Business travel from 0% – 10%.
- Potential exposure to blood‑borne pathogens.
- Requires some lifting and moving of up to 25 pounds.
- Must be able to move between buildings and floors.
- Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day.
- Must be able to read, prepare emails, and produce documents and spreadsheets.
- Must be able to move within…
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