Penumbra
Penumbra

Manufacturing Engineer I (Shift A M-S 6 am a 2 pm)

TLDR

Optimize product quality, equipment performance, and manufacturing processes through hands-on cleanroom engineering under GMP and ISO 13485 standards.

General Summary

The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and support continuous improvement in production. This role focuses on hands-on process engineering in cleanroom environments, collaborating with cross-functional teams to resolve production floor issues and implement improvements. The position involves applying engineering techniques and judgment to optimize product quality, equipment performance, and manufacturing processes in compliance with GMP and ISO 13485 standards.

Qualifications

  • Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering
  • 1+ year of engineering experience.
  • English Level: B2 – Intermediate proficiency required for regular interaction with global teams and documentation in English.
  • Excellent written, verbal and interpersonal communication skills required
  • Engineering experience in a manufacturing environment recommended, medical device industry preferred
  • Knowledge of FDA regulations, Lean/Flow Manufacturing, and/or materials and manufacturing processes desired.
  • Competence using CAD software and MS Office (Excel, PowerPoint, Word).
  • Penumbra is a global healthcare company that designs, develops, manufactures, and markets innovative MedTech solutions aimed at addressing serious medical conditions such as stroke and pulmonary embolism. With a focus on unmet medical needs, Penumbra delivers its novel products directly to hospitals and healthcare providers across major markets, including the U.S., Europe, and Australia.

    Founded
    Founded 2004
    Employees
    500+ employees
    Industry
    Pharmaceuticals
    Total raised
    $120K raised
    View company profile