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 at Moderna. This 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 Do

• Support 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

• 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.

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 real-time collaboration, strong team connections, direct mentorship, and the hands-on partnership needed to deliver our mission. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That's why our co-op benefits are designed to support you during your time with us -at work, at home, and everywhere in between.

• 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

The salary range for this role is $20.00 - $60.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.

• The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.
• The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.