Quality Engineer II

Posted 3 Days Ago
Be an Early Applicant
Cartago, Cartago, CRI
In-Office
Mid level
Healthtech
The Role
Supports Quality Management System activities for medical devices, analyzes quality data, investigates nonconformances, identifies root causes, and drives corrective and preventive actions. Partners with cross-functional teams on continuous improvement, product and process validations, regulatory compliance, and quality control to ensure safe, effective products.
Summary Generated by Built In

Summary

    The Quality Engineer II supports Quality Management System (QMS) activities for new and existing products, manufacturing processes, and quality controls to ensure compliance with regulatory requirements and quality standards. This role analyzes quality data, investigates nonconformances, identifies root causes, and drives corrective and preventive actions to improve product and process performance. Working closely with cross-functional teams, the Quality Engineer II contributes to continuous improvement initiatives, supports product and process validations, and helps ensure the delivery of safe, effective, and high-quality medical devices.

Qualifications

     Requires a bachelor’s degree in engineering or a related field,

    3+ years of experience in quality engineering.

    Proficiency  in English.
     
    Requires familiarity with QSR, ISO, and other applicable regulations and laws.
     
    Manufacturing experience.
     
    Medical device industry experience.
     
    Demonstrates excellent verbal, written, and interpersonal communication skills.
     
    Proficiency in MS Word, Excel, and PowerPoint.

Skills Required

  • Bachelor’s degree in engineering or a related field
  • 3+ years of experience in quality engineering
  • Proficiency in English
  • Familiarity with QSR, ISO, and other applicable regulations and laws
  • Manufacturing experience
  • Medical device industry experience
  • Excellent verbal, written, and interpersonal communication skills
  • Proficiency in Microsoft Word, Excel, and PowerPoint

Penumbra Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Penumbra and has not been reviewed or approved by Penumbra.

  • Healthcare Strength Company materials describe comprehensive medical, dental, and vision coverage with immediate eligibility, alongside life and disability insurance. Feedback suggests health coverage quality is a standout element of the package.
  • Parental & Family Support Company sources indicate fully paid parental leave and on-site support for nursing parents in key locations. Feedback suggests family support policies compare favorably within med‑tech employers.
  • Leave & Time Off Breadth Company postings outline paid holidays, sick leave, and vacation that increases with tenure. Feedback suggests time‑off provisions are broadly competitive when weighing total package value.

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The Company
HQ: Alameda, CA
1,950 Employees
Year Founded: 2004

What We Do

Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need. Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada and Australia, and through distributors in select international markets. The Penumbra logo is a trademark of Penumbra, Inc. Members of the Penumbra team agree that this is where their work has meaning -- we are transforming the treatment of some of the world's most devastating conditions. Penumbra is where everyone's ideas matter, and where learning and growth are constant.

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