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Quality and Regulatory Intern

Job in Madison, Dane County, Wisconsin, 53774, USA
Listing for: Elephas
Apprenticeship/Internship position
Listed on 2026-03-11
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Job Description & How to Apply Below

Elephas is a Madison, WI based biotechnology start-up company working to build an instrument platform that will inform how clinicians treat cancer patients around the world. We are seeking a Quality Assurance Intern who is looking to join a group of motivated people driven to providing hope to cancer patients globally.

We are looking for someone who is actively pursuing a career in Quality Assurance or Regulatory Affairs. The ideal candidate will be self-motivated, eager to learn, and comfortable working in a fast-paced and highly collaborative environment. This is a great opportunity to gain practical, hands-on experience in a growing company.

What Will You Do?
  • Provide QA/RA support to Research and Development and Operations departments in support of new initiatives, products and services
  • Support implementation of continuous improvement projects for the enterprise Quality Management System (eQMS)
  • Draft Standard Operating Procedures (SOPs) and product development documentation
  • Assist in planning efforts of internal and external audits
  • Help create and deliver employee training documents in support of the eQMS
What Will You Need?
  • Be a junior or senior student actively pursuing a STEM degree
  • Have a commitment and passion for product compliance, quality, and safety
  • Have the ability and desire to read, understand, and interpret regulations
  • Computer proficiency with Microsoft Office Suite
  • Strong analytical, critical-thinking and problem-solving skills
  • Detail oriented with strong organizational skills
  • Excellent verbal, interpretation, and written communication skills
  • Strong interpersonal skills and the ability to work cross-functionally
Nice To Have
  • Familiarity with the requirements of the FDA Quality System Regulation 21 CFR Part 820 and ISO 13485 Quality Management System - Medical Devices
Benefits
  • Practical experience with varied business activities
  • Shadowing, mentoring, and training with experienced and accomplished professionals
  • Competitive compensation
  • Flexible schedule
  • Collaborative and supportive work environment
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