Co-Op, Quality Assurance & Compliance

ModernaTX • Norwood, MA

7d • Onsite

About The Position

This winter/spring co-op is based at Moderna’s Norwood, Massachusetts site and runs from January 18, 2027, through June 25, 2027. Applicants must be available for the full co-op duration. The Quality Assurance Co-op will join a team supporting internally produced cGMP materials and gain hands-on exposure to quality oversight activities and Moderna’s Quality System. The role partners with experienced team members to support compliant manufacturing operations and global regulatory expectations. It is 100% onsite and is not eligible for remote work.

The co-op supports quality-system activities, document and batch-record review, manufacturing compliance, investigations, inspection readiness, and quality metrics. The role also contributes to improvement projects and may lead assigned quality projects with guidance. Candidates must already have U.S. work authorization and be able to maintain it without future sponsorship. Due to export-control requirements, only U.S. persons—citizens, permanent residents, asylees, or refugees—are eligible.

Requirements

• Currently enrolled in a bachelor’s or master’s program in a science-related field 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 willingness to ask questions and appropriately escalate quality or safety concerns.
• Must be available for the entire co-op duration, January 18, 2027, through June 25, 2027.
• Must already hold U.S. work authorization and be able to maintain that status without future sponsorship.
• Must qualify as a U.S. person under U.S. export-control requirements: a U.S. citizen, permanent resident, asylee, or refugee.

Nice To Haves

• GPA of 3.5 on a 4.0 scale or equivalent.
• Ability to work independently and contribute to high-performing teams.
• Excellent written and verbal communication skills.
• Desire to make an impact at a high-growth, transformational company described as Bold, Relentless, Curious, and Collaborative.

Responsibilities

• 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.
• Perform additional duties as assigned.

Benefits

• Free premium access to meditation and mindfulness classes.
• Subsidized commuter benefits.
• Paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown.
• Location-specific perks and extras.
• May be eligible for an annual discretionary bonus, other incentive compensation, or an equity award, subject to plan eligibility criteria and individual performance.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern