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Moderna

Develops mRNA-based medicines for health

Compliance and Data QC Co-op

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Internship · Winter 2027, Spring 2027Norwood, MA, USA

About the Job

Requirements

  • Currently enrolled in a Bachelor's or Master's degree program in a STEM field, such as Biology, Biochemistry, Molecular Biology, Chemical Engineering, or a related discipline.
  • Have foundational laboratory, compliance, and quality skills applicable to analytical testing.
  • Must already hold U.S. work authorization and be able to maintain that status without future sponsorship.
  • A GPA of 3.5 on a 4.0 scale or equivalent academic achievement is preferred.
  • Be able to work independently while contributing effectively within a team environment.
  • Have strong written and verbal communication skills.
  • Have high attention to detail and a commitment to quality and compliance.
  • Have an interest in working within a regulated laboratory environment.

Responsibilities

  • Support laboratory compliance activities within the CBL in alignment with GCLP guidelines, applicable procedures, and quality requirements.
  • Assist with review and organization of laboratory governance documents, SOPs, forms, worksheets, and compliance records to support document accuracy, traceability, and readiness for use.
  • Support training compliance activities, including review and organization of training records and follow-up of documentation to help maintain complete and current records.
  • Assist with documentation, tracking, data gathering, and follow-up activities related to Quality Event and issue management processes under the guidance of the Compliance team.
  • Support audit and inspection readiness activities, including document preparation, request tracking, record organization, and other logistical support for internal or external assessments.
  • Assist with review of laboratory documentation for good documentation practices and ALCOA+ principles, including attributable, legible, contemporaneous, original, accurate, complete, consistent, enduring, and available records.
  • Collaborate with laboratory scientists, study teams, Compliance, and other cross-functional partners to support day-to-day compliance activities and project deliverables.
  • Contribute to special projects that strengthen laboratory quality systems and provide exposure to compliance within a regulated clinical laboratory environment.

About the Company

Moderna

Develops mRNA-based medicines for health

Moderna develops medicines built on messenger RNA (mRNA). Its products use mRNA delivered into cells to instruct them to produce specific proteins that can prevent or treat disease, with vaccines being a primary example. In practice, a dose delivers engineered mRNA into the body, cells translate it into a target protein, and the immune system responds or the protein modulates biology to combat disease. Moderna differentiates itself through its focus on building a whole mRNA medicines platform and in-house capabilities for designing, manufacturing, and scaling mRNA therapies, including rapid development and large-scale production. Its goal is to create a new category of medicines based on mRNA that can improve how diseases are discovered, developed, and treated, ultimately improving patient outcomes.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2010

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