The Role
We are seeking a highly motivated Automation Engineering Co-Op / Intern to support Global Drug Product Automation initiatives focused on Visual Inspection (VI) systems automated and semi-automated inspection equipment and manufacturing system integration.
This role sits at the intersection of automation engineering machine vision manufacturing operations and data/system integration. The co-op will support the Automated Visual Inspection (AVI) platforms (including Switch 350 and systems) assisting with equipment integration network configuration SCADA connectivity and data analysis efforts supporting global Drug Product operations.
This is a hands-on learning opportunity to understand how complex inspection systems are deployed validated and integrated into regulated pharmaceutical manufacturing environments.
Heres What Youll Do
Visual Inspection Systems
Support automated and semi-automated Koerber AVI systems (Switch 350 )
Assist with system configuration troubleshooting and operational support
Review and analyze inspection results defect classifications and performance trends
Support data reviews related to VI performance across global manufacturing sites
Assist with documentation to support commissioning qualification and validation activities
Automation & Systems Integration
Support integration of VI systems into manufacturing networks
Assist with IP configuration network connectivity and system communication troubleshooting
Support SCADA integration and data exchange with site automation systems
Assist in aligning vendor systems with internal automation and data standards
Participate in cross-functional discussions with Manufacturing IT Quality and vendors
Data & Analysis
Review and analyze inspection data from global manufacturing sites (including Australia)
Identify trends data gaps and opportunities for standardization or improvement
Assist in organizing and presenting data for engineering and operational review
Support efforts to improve data accessibility and usability for manufacturing teams
What Youll Learn
How automated and semi-automated visual inspection systems operate in pharmaceutical manufacturing
How machine vision systems are integrated into plant automation and IT networks
How inspection data supports product quality compliance and operational decision-making
How regulated manufacturing environments manage system integration and validation
How cross-functional teams collaborate to deploy and support complex automation systems
Heres What Youll Need (Basic Qualification)
Currently pursuing a Bachelors or Masters degree in:
Electrical Automation Mechanical Computer or Industrial Engineering (preferred)
Computer Science or related technical field
Strong interest in automation manufacturing systems or industrial technology
Comfortable working with technical systems and structured data
Strong analytical and problem-solving skills
Able to communicate technical concepts clearly and professionally
Curious self-driven and eager to learn in a regulated manufacturing environment
This position is site-based requiring you to be at Modernas 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.
Heres What Youll Bring to the Table (Preferred Qualification)
Exposure to manufacturing automation machine vision or industrial systems
Interest in pharmaceutical or regulated manufacturing environments
- Experience working on technical projects involving hardware and software integration
Pay & Benefits
At Moderna we believe that when you feel your best you can do your best work. Thats 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.
About Moderna
Since our founding in 2010 we have aspired to build the leading mRNA technology platform the infrastructure to reimagine how medicines are created and delivered and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission values and mindsets every day our people are the driving force behind our scientific progress and our culture. Together we are creating a culture of belonging and building an organization that cares deeply for our patients our employees the environment and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer a Fast Company Best Workplace for Innovators and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine we invite you to visit to learn more about our current opportunities.
Our Working Model
As we build our company we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation teamwork and direct mentorship. 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.
Equal Opportunities
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry or citizenship ethnicity disability military or protected veteran status genetic information sexual orientation marital or familial status or any other personal characteristic protected under applicable is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories consistent with legal requirements.
Accommodations
Were focused on attracting retaining developing and advancing our employees. By cultivating a workplace that values diverse experiences backgrounds and ideas we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at .
Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws including the Export Administration Regulations (EAR). As such employment is contingent upon the applicants ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements only individuals who qualify as U.S. persons (citizens permanent residents asylees or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.
Learn how we’re changing the world of medicine. Discover career opportunities, our product pipeline, and browse media resources. Meet Moderna.