2026 Co-Op, Quality Control Bioassays
The Role
This is a full-time summer internship based in Norwood, MA from July 13th-December 11th, 2026. Candidates must be available for the entire duration of the program.
The QC Bioassay Summer Intern will support laboratory operations within Moderna’s GMP Quality Control laboratories at the Norwood manufacturing site and affiliated contract organizations. The internship provides hands-on exposure to molecular and cell biology techniques, GMP documentation practices, and QC laboratory operations supporting raw materials, drug substance, and drug product testing.
This role offers meaningful, practical experience in a regulated biopharmaceutical environment, with the opportunity to contribute to ongoing laboratory and operational initiatives.
Here’s What You’ll Do
Partner with experienced QC scientists to learn and apply core bioassay laboratory techniques.
Prepare reagents, solutions, and materials required for routine laboratory testing.
Support equipment maintenance, laboratory organization, and general housekeeping activities.
Assist with ordering, receiving, and inventory management of laboratory supplies.
Perform data management activities, including scanning, uploading, and organizing GMP records.
Adhere to Good Documentation Practices (GDP) and Data Integrity requirements to ensure accurate, complete, and inspection-ready records.
Maintain a safe laboratory environment and follow all site safety and compliance requirements.
Complete all required training assignments in a timely manner.
Contribute to special projects and continuous improvement initiatives as assigned
Here’s What You’ll Need (Basic Qualifications)
Currently enrolled in a Bachelor’s or Master’s degree program in a STEM field (e.g., Biology, Biochemistry, Molecular Biology, Chemical Engineering, or related discipline).
Foundational laboratory skills applicable to bioprocessing or analytical testing
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 .
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 Bring to the Table (Preferred Qualifications)
GPA of 3.5 (on a 4.0 scale) or equivalent academic achievement.
Demonstrated ability to work independently while contributing effectively within a team environment.
Strong written and verbal communication skill.
High attention to detail and commitment to quality and compliance.
Interest in working within a GMP-regulated biopharmaceutical manufacturing environment.
A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.
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.
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 modernatx.com/careers 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 person's 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 law. Moderna 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
We’re 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 [email protected] .
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 applicant’s 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.Recommended Jobs
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