2026 Co-Op, Quality Control Bioassays

ModernaTXNorwood, MA
4d$20 - $60Onsite

About The Position

The Role This is a full-time summer internship based in Norwood, MA from July 13th-December 11th, 2026. Candidates must be available for the entire duration of the program. The QC Bioassay Summer Intern will support laboratory operations within Moderna’s GMP Quality Control laboratories at the Norwood manufacturing site and affiliated contract organizations. The internship provides hands-on exposure to molecular and cell biology techniques, GMP documentation practices, and QC laboratory operations supporting raw materials, drug substance, and drug product testing. This role offers meaningful, practical experience in a regulated biopharmaceutical environment, with the opportunity to contribute to ongoing laboratory and operational initiatives.

Requirements

  • Currently enrolled in a Bachelor’s or Master’s degree program in a STEM field (e.g., Biology, Biochemistry, Molecular Biology, Chemical Engineering, or related discipline).
  • Foundational laboratory skills applicable to bioprocessing or analytical testing
  • Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship .
  • This position is site-based, requiring you to be at Moderna’s site full-time.
  • This position is not eligible for remote work.

Nice To Haves

  • GPA of 3.5 (on a 4.0 scale) or equivalent academic achievement.
  • Demonstrated ability to work independently while contributing effectively within a team environment.
  • Strong written and verbal communication skill.
  • High attention to detail and commitment to quality and compliance.
  • Interest in working within a GMP-regulated biopharmaceutical manufacturing environment.
  • A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Responsibilities

  • Partner with experienced QC scientists to learn and apply core bioassay laboratory techniques.
  • Prepare reagents, solutions, and materials required for routine laboratory testing.
  • Support equipment maintenance, laboratory organization, and general housekeeping activities.
  • Assist with ordering, receiving, and inventory management of laboratory supplies.
  • Perform data management activities, including scanning, uploading, and organizing GMP records.
  • Adhere to Good Documentation Practices (GDP) and Data Integrity requirements to ensure accurate, complete, and inspection-ready records.
  • Maintain a safe laboratory environment and follow all site safety and compliance requirements.
  • Complete all required training assignments in a timely manner.
  • Contribute to special projects and continuous improvement initiatives as assigned

Benefits

  • Free premium access to meditation and mindfulness classes
  • Subsidized commuter benefits
  • Generous paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown
  • Location-specific perks and extras
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