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Internship

Quality Engineering Intern - Summer 2024

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Inari Medical

‚ÄĘ

3mo ago

ūüöÄ Summer Internship

Irvine

‚Ćõ Closed
Applications are closed

Summer Internship

Software Engineering‚ÄĘIrvine

Description

  • Get ready for an immersive 12-week experience with our Summer Internship Program at Inari Medical! This program will offer students a unique opportunity to dive headfirst into the world of medical devices, where cutting-edge technology meets medical innovation.  
  • This is not just an internship; it's a chance to learn from and work alongside our Clot Warriors to make an impact on patients' lives.   
  • As a Quality Engineering Intern, you will have the opportunity to work closely with our experienced Quality Engineering team and gain hands-on experience in ensuring the highest standards of quality for our medical devices. This internship is designed to provide exposure to various aspects of quality engineering within the medical device industry.   

Requirements

  • Currently pursuing a degree in Engineering, Quality Management, or a related field.
  • Enrolled as a student for the duration of the internship program. Graduating December 2024 or later.
  • Maintain a minimum GPA of 3.0 or higher.
  • Strong interest in quality engineering within the medical device industry.
  • Knowledge of quality standards and regulations (e.g., ISO 13485, FDA regulations) preferred.
  • Detail-oriented with excellent organizational and analytical skills.
  • Effective communication and teamwork skills.

Education requirements

Currently Studying

Area of Responsibilities

Software Engineering

Responsibilities

  • Assist in maintaining and improving the Quality Management System (QMS) to ensure compliance with relevant standards and regulations.
  • Support the execution of quality control activities, including inspection, testing, and documentation of results.
  • Contribute to risk management activities, including the identification, assessment, and mitigation of risks associated with medical device development.
  • Assist in managing and organizing quality-related documentation, ensuring accuracy and compliance with established procedures.
  • Collaborate with the team to assess and monitor the performance of suppliers to maintain a high level of quality in the supply chain.
  • Participate in the investigation and resolution of quality issues through the CAPA process.
  • Contribute to continuous improvement initiatives by identifying opportunities to enhance processes and systems.

Details

Work type

Full time

Work mode

office

Location

Irvine