QA Validation & Qualification Intern – Summer 2027 (Onsite)

Regeneron Pharmaceuticals, Inc.

City of Rensselaer (NY)

On-site

USD 25,000 - 35,000

Full time

24 hours ago
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Benefits offered by this job

Health insurance
Paid time off
On-site work

Job summary

Regeneron Pharmaceuticals, Inc. in the United States seeks a 2027 Summer Intern for Quality Assurance – Validation & Qualification. Interns work onsite from May/June through August, with pay determined by education level and degree program.

The hourly rate ranges from $17.90 to $25.50, depending on education and program level. Responsibilities include verifying equipment inventories and validation records, supporting cleaning validation and aseptic process simulations, and assisting with

Qualifications

  • Must be enrolled in an academic program pursuing an Undergraduate or Graduate degree and be returning to school the semester following the position or graduating after the position.
  • Cumulative GPA of 3.0 or higher preferred

Responsibilities

  • Verify equipment inventories, labeling, and validation records in asset-management systems.
  • Support cleaning validation and verification, aseptic process simulations (media fills), and shipping/transport validation.
  • Help improve qualification of components and raw materials (sampling plans, defect classification, supplier communication).
  • Run gap assessments against industry standards (ISO/ISPE) and review historical qualification records for recurring issues.
  • Assist with tools/systems development for qualification programs and pilot emerging tech in a regulated environment.

Education

Pursuing Undergraduate or Graduate degree

Job description

Regeneron Pharmaceuticals, Inc. in the United States seeks a 2027 Summer Intern for Quality Assurance – Validation & Qualification. Interns work onsite from May/June through August, with pay determined by education level and degree program.

The hourly rate ranges from $17.90 to $25.50, depending on education and program level. Responsibilities include verifying equipment inventories and validation records, supporting cleaning validation and aseptic process simulations, and assisting with

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