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Penumbra Inc

Neurovascular and peripheral medical devices manufacturer

Especialista de Servicios de Documentación 1

Validation, Compliance & Quality SystemsPosted on Nov 12
Full-timeCartago Province, Cartago, Costa RicaNo salary listedIn-person

About the Job

Requirements

  • Be an advanced student in Business Administration, Industrial Engineering, Process Engineering, or a similar field.
  • Have 1 year of experience in medical-industry manufacturing environments.
  • Have intermediate English reading proficiency to handle documentation.
  • Have basic knowledge of QSR, ISO, and other regulations.
  • Have intermediate proficiency in Microsoft Word, Excel, and PowerPoint.

Responsibilities

  • Support document-control processes and quality-records management, ensuring physical and electronic documentation remains complete, accurate, current, and compliant with internal procedures and regulatory requirements.
  • Support training-records management and Good Documentation Practices (GDP) reviews.
  • Prepare documentation for audits.

Desired Qualifications

  • A technician qualification in Quality or Business Administration.

About the Company

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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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