Senior Development & Manufacturing Engineer

Penumbra, Inc.

San Francisco (CA)

On-site

USD 109,000 - 152,000

Full time

41 hours ago
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Benefits offered by this job

Medical benefits
Dental benefits
Vision benefits
401(k) match
Parental leave
Company holidays
Vacation

Job summary

Penumbra, Inc. in Alameda, CA is seeking an engineer to join our team, executing detailed projects in a manufacturing environment.

You will analyze complex problems, perform root cause analysis, and coordinate cross-functional efforts to deliver innovative solutions. The role involves leading supplier-level project implementations, developing processes and fixtures, and ensuring compliance with QMS and FDA-related requirements.

Qualifications

  • Engineering degree with 2+ years relevant experience in manufacturing.
  • Experience in medical device manufacturing preferred.
  • Familiarity with FDA regulations and Lean/Flow Manufacturing.
  • Proficient in MS Office applications.

Responsibilities

  • Solve complex problems and implement innovative solutions.
  • Perform root cause analysis and propose vetted solutions.
  • Communicate problems and solutions cross-functionally.
  • Lead supplier-level project implementations and track milestones.
  • Develop and validate processes and equipment; document results.
  • Adhere to QMS and related quality standards.

Skills

Complex problem solving
Root cause analysis
Cross-functional communication
Project coordination
Quality systems knowledge

Education

Bachelor's degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering

Tools

Word
Excel
PowerPoint
Access

Job description

Penumbra, Inc. in Alameda, CA is seeking an engineer to join our team, executing detailed projects in a manufacturing environment.

You will analyze complex problems, perform root cause analysis, and coordinate cross-functional efforts to deliver innovative solutions. The role involves leading supplier-level project implementations, developing processes and fixtures, and ensuring compliance with QMS and FDA-related requirements.

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