This Co-op intern role is within the Global Engineering organization and will serve a key role within the team supporting the Electronic Batch Record (EBR) designing, authoring, documenting and testing to deliver MES (Manufacturing Execution system) EBR for the drug product manufacturing processes. The individual will support and execute in project mode translating process requirements and MES system best practices into practical, usable electronic batch records. This role offers working experience in the MES space and exposure to the manufacturing processes of medicines. This position will run from July 13th-Dec 11th 2026
You will work alongside experienced MES engineers in a fast-paced, collaborative environment, gaining exposure to MES EBR authoring, EBR execution, and systems integration for manufacturing processes.
Here’s What You’ll Do
Primarily perform MES recipe design and authoring by following best practices and perform impact assessment
Support configuration of master data in the system
Directly support operations with EBR execution on the floor, troubleshooting and issue resolution with respect to MES and automation systems
Participates in validation activities in conjunction with IT, Validation, Manufacturing, and QA related to implementation and on-going support.
Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.
Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.
Here’s What You’ll Need (Basic Qualifications)
Education: An undergrad or grad program in Engineering, Computer Science, or other technical degrees
Strong fundamental scientific and engineering skills
Familiarity with at least one programming language
Curiosity about process, automation and MES systems
Strong problem-solving skills, willingness to learn, and ability to work in a team.
Ability to work effectively in a team-oriented environment
Demonstrated aptitude or ability to learn to gain a strong understanding of GxP regulations
This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work.
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.
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 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.
2026 Co-Op, Process Automation and Drug Product • Norwood, Massachusetts