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Penumbra Inc

Neurovascular and peripheral medical devices manufacturer

Development Quality Engineer 1

Quality EngineeringConfirmed live in the last 24 hours
Full-timeAlameda, CA, USA$80k - $105k /yrIn-person

About the Job

Requirements

  • Associate’s or Bachelor’s degree in Engineering, a Life Science, or a related field, plus quality engineering or relevant experience, preferably in a medical device environment, or an equivalent combination of education and experience.
  • Familiarity with QSR, ISO, and other applicable regulations and laws is required.
  • Proficiency with Microsoft Word, Excel, and PowerPoint is required.
  • Ability to perform duties in office, laboratory, and cleanroom environments, including potential exposure to blood-borne pathogens and lifting and moving up to 25 pounds.
  • Ability to move between buildings and floors, remain stationary and use standard office equipment for extended periods, move within the office and access supplies, and read, prepare emails, produce documents and spreadsheets, and communicate and exchange accurate information with employees at all levels.

Responsibilities

  • Participate in product development and qualification activities for new and existing products.
  • Participate in product development teams.
  • Develop testing and inspection methodologies and documentation for new and existing products.
  • Design and install quality sampling systems and procedures using statistical analysis.
  • Design or specify inspection and testing equipment to meet product requirements.
  • Perform failure analyses and defect investigations.
  • Analyze and apply design control standards.
  • Recommend revisions to specifications, procedures, and work instructions for device design and process improvement.
  • Interface with internal departments, customers, and suppliers on product- and quality-related issues.
  • Adhere to the Company’s Quality Management System, as well as applicable domestic and global quality system regulations, standards, and procedures.
  • Understand relevant security, privacy, and compliance principles and adhere to applicable regulations, standards, and procedures.
  • Ensure other department members follow the Quality Management System, regulations, standards, and procedures.
  • Perform other work-related duties as assigned.

Desired Qualifications

  • Quality engineering or relevant experience, preferably in a medical device environment.

About the Company

Penumbra Inc

Neurovascular and peripheral medical devices manufacturer

Penumbra Inc. designs, develops, and sells medical devices for neurovascular and peripheral vascular conditions. Its products are used by doctors in hospitals and clinics and work by being inserted into blood vessels to remove clots, support catheter-based procedures, or help reconstruct vessels. The company differentiates itself with a broad, integrated portfolio across neurovascular and peripheral interventions and a global sales network that serves Europe and the Americas. Its goal is to improve patient outcomes through high-quality tools and ongoing research and development to expand capabilities.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Alameda, CA
Founded
2004

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