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Intern, Quality Engineering

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Werfen

23d ago

  • Internship
    Full-time
    Summer Internship
  • Research & Development
    Engineering
  • San Diego

AI generated summary

  • You must be enrolled in a Bachelor's or Graduate program with a 3.0 GPA, and have a basic understanding of quality engineering, GMP, GDP, and metrology principles.
  • You will write quality documents, engage in process validation, resolve product issues, investigate non-conformances, assess risks, and prioritize urgent tasks. Additional duties as assigned.

Requirements

  • Currently enrolled in a Bachelor's or Graduate program with a minimum GPA of 3.0
  • Basic understanding on quality engineering principles including root cause investigation is desired.
  • Basic understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) is desired
  • Basic understanding of metrology principles is desired

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

FAQs

What is the duration of the internship program?

The internship program lasts for 10 weeks.

What are the responsibilities of a Quality Engineering Intern?

The main responsibilities include writing quality system documents, participating in process validation teams, investigating non-conformances, conducting risk evaluations, and performing other assigned duties related to quality engineering.

What qualifications are required for this internship position?

Candidates must be currently enrolled in a Bachelor's or Graduate program with a minimum GPA of 3.0, and have a basic understanding of quality engineering principles, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and metrology principles.

What key attributes are expected from an intern in this role?

Interns should have confidence in using Microsoft Word and Excel, demonstrate enthusiasm and initiative, be able to review process procedures, perform research to improve process quality, conduct experiments, analyze data, and summarize findings effectively.

Will I be working with other departments during the internship?

Yes, you will have the opportunity to work cross-functionally with other departments to maximize your learning experience.

What kind of pay can I expect during this internship?

The pay range for this position is currently $24-$28 per hour, based on the candidate's qualifications, experience, and other relevant factors.

Is previous experience in quality engineering required for the internship?

No previous experience is strictly required, but a basic understanding of quality engineering principles and practices is desired.

Will I receive training during the internship?

Yes, the internship program is designed to provide hands-on experience and training in quality engineering activities.

Are there opportunities for networking during the internship?

Yes, you will be able to network with various departments including Manufacturing, Regulatory Affairs, Research and Development, and Quality Control.

What types of projects might I work on as an intern?

Interns may participate in process and product development, root cause investigations, risk assessments, verification/validation tasks, and continuous improvement projects.

Manufacturing & Electronics
Industry
5001-10,000
Employees
1966
Founded Year

Mission & Purpose

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.