Logo of Huzzle


• Starts Jun 2

Quality Engineering Internship

Logo of Werfen


1mo ago

🚀 Summer Internship

San Diego

AI generated summary

  • Enrolled in bachelor's or graduate degree program with a minimum GPA of 3.0, excellent communication skills, knowledge of quality engineering principles, cGMP/GDP familiarity, and basic metrology understanding. No travel required.
  • The Quality Engineering Intern will write quality system documents, perform process validation, investigate non-conformances, conduct risk evaluations, prioritize urgent matters, and work cross-functionally to solve quality issues. They will also build key relationships with various departments including Manufacturing, Regulatory Affairs, and R&D.

Summer Internship

EngineeringSan Diego


  • Werfen’s San Diego Internship Program is a 10-week, full-time, paid assignment that takes place over the course of the summer and is open to undergraduate students who are currently pursuing a degree from an accredited college or university. 
  • The Internship program has been designed to allow students to learn through hands on experience, providing an opportunity to blend textbook knowledge with practical experience. Students will contribute to the development of new or improved medical diagnostic tests and will be given the opportunity to work cross functionally with other departments to maximize their learning opportunities.


  • Minimum Knowledge & Experience required for the position:
  • Currently enrolled in a bachelor’s or graduate degree program with a minimum GPA of 3.0.
  • Skills & Capabilities:
  • Excellent written and verbal communication skills are required.
  • Basic understanding of quality engineering principles including root cause investigation is desired.
  • Basic understanding of current Good Manufacturing Practices (cGMP) & Good Documentation Practices (GDP) is desired.
  • Basic understanding of metrology principles is desired.
  • Travel requirements:
  • No travel needed.

Education requirements

Currently Studying

Area of Responsibilities



  • Write quality system documents which comply with applicable regulations and standards
  • Participate on process validation teams
  • Work cross-functionally, as a key resource, to solve problems related to product or process quality issues; investigate non-conformances, identify root cause, and determine/implement appropriate corrective action plans
  • Conduct risk and trend evaluations for product non-conformances
  • Ability to prioritize urgent matters
  • Other duties as assigned
  • Networking/Key relationships:
  • Manufacturing/Operations
  • Manufacturing Engineering
  • Regulatory Affairs
  • Research and Development
  • Biomedical Quality Control Lab
  • Incoming Quality Control Lab


Work type

Full time

Work mode


Start date

Jun 2, 2024


San Diego