Co-Op, Quality Assurance & Compliance

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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 hiringPaidWinter 2027Spring 2027Biotechnology Research
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    Best applied by Oct 18

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    About the role#

    This is a full-time co-op position based in Norwood, Massachusetts. You will work with the Quality Assurance team to support cGMP materials produced internally. This role provides hands-on experience with quality oversight and Moderna’s Quality System while partnering with team members to meet global regulatory expectations. The co-op runs from January 18, 2027, through June 25, 2027.

    What you'll do#

    • Support compliance activities and learn the fundamentals of quality systems.
    • Collaborate with Quality and cross-functional teams on daily tasks and improvement projects.
    • Draft and review SOPs, policies, batch records, testing records, and training materials.
    • Review electronic and paper batch records for completeness and cGMP compliance.
    • Observe manufacturing activities and support compliance with procedures, specifications, and cleanroom practices.
    • Maintain clear, accurate, and complete documentation while following data integrity principles.
    • Identify and escalate manufacturing, safety, and quality concerns.
    • Support deviation documentation, investigations, and corrective actions.
    • Assist with regulatory and inspection readiness, including internal audits and health authority engagement.
    • Collect, analyze, and report quality metrics to identify trends.
    • Lead assigned quality projects from planning through completion.
    • Manage priorities across multiple projects simultaneously.
    • Follow safety procedures and practice safe work habits.

    What you'll need#

    • Current enrollment in a Bachelors or Masters program in a Science-related field or Regulatory Affairs.
    • Interest in cGMP manufacturing, quality systems, batch record review, deviation management, and inspection management.
    • Strong written and verbal communication skills.
    • Attention to detail and a collaborative mindset.
    • Willingness to ask questions and escalate concerns appropriately.
    • Ability to work both independently and as part of a high-performing team.
    • A GPA of 3.5 on a 4 scale or equivalent is preferred.
    • Must hold current work authorization in the U.S. as sponsorship is not available for this role.

    Location & details#

    • Location: Norwood, Massachusetts.
    • Modality: 100% on-site. This role is not eligible for remote work.
    • Duration: January 18, 2027 - June 25, 2027.
    • Compensation: $20.00 - $60.00 per hour, plus potential for discretionary bonus or incentive compensation.
    • Benefits: Includes subsidized commuter benefits, paid time off, and access to mindfulness resources.
    Relevant fieldsOther

    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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