2027 Summer Intern Quality Assurance – Compliance & Quality Systems (IOPS)
About The Position
Regeneron is seeking multiple 2027 interns for its Quality Assurance – Compliance & Quality Systems teams within Industrial Operations and Product Supply (IOPS). Quality Assurance helps ensure manufacturing processes are documented, controlled, and operating correctly, and that deviations are investigated and corrected. The role offers the opportunity to contribute to a science-driven organization developing medicines for serious diseases. Intern projects may involve analyzing deviation, exception, and quality-signal data to identify trends; developing standard language, trackers, and templates for consistent, audit-ready documentation; and improving change management, annual product quality review, and other compliance processes. Interns may also support regulatory submissions, health authority information requests, and partner notifications. Other potential projects include creating job aids, reviewer guides, onboarding and training materials, harmonized compliance matrices and medical-device quality templates, and small business tools or dashboards for visualizing change controls. The work commonly combines data analysis, technical writing, process mapping, and cross-functional collaboration. Lab work is none to minimal, and the roles are largely desk-based. The internships are full-time and onsite in Rensselaer, East Greenbush, or Troy, New York, from May or June through August.
Requirements
- Must be enrolled in or accepted to an undergraduate or graduate academic program and be returning to school the semester after the internship, or graduating after the internship.
- Relevant fields of study include Biology, Chemistry, Pharmacy, Biomedical Engineering, Chemical Engineering, Mechanical Engineering, Computer Science/Information Technology, Statistics/Data Science, and Supply Chain/Industrial Engineering.
Nice To Haves
- Demonstrated leadership through campus activities, clubs, sports, current or previous work, or community involvement.
- Cumulative GPA of 3.0 or higher.
Responsibilities
- Analyze deviation, exception, and quality-signal data to identify trends.
- Develop standard language, trackers, and templates to support consistent, audit-ready documentation.
- Help improve change management, annual product quality review, and other compliance processes.
- Support regulatory submissions, health authority information requests, and partner notifications.
- Create practical tools and guidance, including job aids, reviewer guides, onboarding and training materials, compliance matrices, medical-device quality templates, and dashboards.
- Participate in data work, technical writing, process mapping, and cross-functional collaboration.
Benefits
- Competitive and comprehensive total rewards package, which may include annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, medical, dental, vision, life and disability insurance, paid time off, and family support benefits.
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
No Education Listed
