Intern - Quality Assurance Coordinator

Revvity•San Diego, CA

2d•$20 - $24

About The Position

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health. Find your future at Revvity Join the Quality Assurance team at BioLegend to support core Quality Management System (QMS) activities in a regulated biotech setting. You’ll help with document control, training records, and validation documentation within our eQMS, while gaining exposure to ERP-related quality workflows. Under mentorship, you’ll build practical knowledge of standards such as ISO 13485 and FDA 21 CFR 820 and learn how quality processes drive reliable products.

Requirements

Currently pursuing a Bachelor’s degree

Nice To Haves

Coursework or hands-on experience with GMP/GLP principles or quality systems in an academic or lab environment.
Proficiency with Microsoft Word and Excel, with strong attention to detail and document organization.
Familiarity with ISO 13485, FDA 21 CFR 820, or MDSAP frameworks.
Experience using eQMS or document control tools (e.g., SmartSolve) and Adobe Acrobat; PowerPoint skills for summaries/presentations.
Strong analytical, communication, and time-management skills; ability to work independently and in a team.

Responsibilities

Process document control requests and maintain training records in the eQMS.
Assist with equipment and process validation documentation, change control, and record reviews.
Compile and organize QMS metrics for monthly reports and management reviews.
Support internal and external audit preparation, logistics, and follow-up documentation.
Partner with cross-functional teams (Manufacturing, R&D/PD, QC, IT, Supply Chain) to uphold quality procedures.