Intern, Quality Assurance

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    Moderna

    Our mission is to deliver the greatest possible impact to people through mRNA medicines.

    1,001-5,000 employeesFounded 2010Cambridge, MassachusettsBiotechnology Research
    Actively hiringPaidSummer 2027Biotechnology Research
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    About the role#

    The Quality Assurance Intern will support Quality operations and Quality Systems at the Moderna cGMP manufacturing facility in Laval, Canada. This full-time internship provides practical exposure to Good Manufacturing Practices (GMP), controlled documentation, training administration, and records management within a regulated biopharmaceutical environment. You will work alongside experienced Quality professionals and cross-functional partners to maintain accurate, organized, and inspection-ready documentation. This role is designed to provide professional experience in Quality Assurance operations.

    What you'll do#

    • Support document control and records-management activities, including scanning, filing, archiving, and retrieval of GMP records.
    • Assist with training administration, including tracking assigned training and supporting compliance reports.
    • Help prepare, format, and maintain controlled documents such as SOPs, work instructions, and forms.
    • Assist with periodic reviews of Quality documentation and trackers to ensure they remain current and accurate.
    • Support the review and organization of electronic and paper GMP documentation for adherence to Good Documentation Practices.
    • Maintain Quality metrics, dashboards, trackers, and meeting materials.
    • Participate in Quality meetings and governance forums, including capturing actions and supporting follow-up activities.
    • Support data gathering and document retrieval for audits, inspections, and compliance walkthroughs.
    • Identify and communicate potential documentation or process gaps to the Quality team.
    • Support continuous-improvement initiatives focused on documentation practices and operational efficiency.
    • Partner with Quality, Manufacturing, and Digital/IT teams on assigned projects.
    • Complete all required training assignments and contribute to special projects.

    What you'll need#

    • Currently enrolled in a Bachelor’s or Master’s degree program in a science, engineering, pharmacy, quality, life-sciences, or related discipline.
    • Basic proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook.
    • Ability to work carefully with controlled records and follow written procedures in a regulated environment.
    • Ability to work on-site at the Moderna Laval facility for the duration of the internship.

    Location & details#

    • Location: Laval, Quebec, Canada.
    • Term: Summer 2027 (May to August).
    • Modality: On-site, full-time.

    About Moderna

    Moderna operates in the biotechnology research sector. Founded in 2010, the company focuses on the development of mRNA therapeutics and vaccines. It maintains headquarters in Cambridge, Massachusetts. The organization employs between 1,001 and 5,000 people and functions as a public company.

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