2026 Co-Op, Process Automation and Drug Product
About The Position
The Role: 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.
Requirements
- 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.
- Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.
Responsibilities
- 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.
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Intern
