Co-Op, Quality Assurance & Compliance

The Role This is a winter / spring co-op opportunity in Norwood, MA from January 18, 2027 – June 25, 2027. Applicants must be available for the entire duration of the co-op. Start date will be January 18, 2027.The Quality Assurance Co-op will be part of a cohesive team supporting cGMP materials produced internally s role will provide hands-on exposure to quality oversight activities and Moderna’s Quality System while partnering with experienced team members to support compliant manufacturing operations and global regulatory expectations.

This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work.

Here’s What You’ll DoSupport compliance activities and learn the fundamentals of quality systems.

Collaborate with Quality and cross-functional teams on daily activities and improvement projects.

Help 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.

Follow written procedures and maintain clear, accurate, and complete documentation.

Complete required training and follow data integrity principles.

Identify and promptly escalate manufacturing, safety, and quality concerns.

Support deviation documentation, investigations, and corrective actions.

Support regulatory and inspection readiness activities, including internal audits and health authority engagement.

Collect, analyze, and report quality metrics to identify trends and improvement opportunities.

Use problem-solving skills to support quality and operational improvements.

Lead assigned quality projects from planning through completion with guidance.

Manage priorities and contribute to multiple projects at the same time.

Follow Moderna’s safety procedures and practice safe work habits.

Additional duties as assigned.

Here’s

What You’ll Bring to the Table (Basic Qualifications)
Current student enrolled in a Bachelors or Masters program in Science related fields or Regulatory Affairs.

Interest in learning about cGMP manufacturing, quality systems, batch record review, deviation management, and inspection management.

Strong written and verbal communication skills, attention to detail, a collaborative mindset, and a willingness to ask questions and escalate quality or safety concerns appropriately.

At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.

Here’s

What You’ll Bring to the Table (Preferred Qualifications)
GPA of 3.5 on a 4 scale or equivalent.

Demonstrated ability to work both independently as well as the ability to contribute to high performing teams.

Excellent written and verbal communication skills.

A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.

Our Working Model As we build our company, we have always believed that an in-person culture is critical to our success. This role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site-based operations.

Working onsite enables…