2026 Co-op, R&D Quality (GxP)

The Role

This is a fall Co-op opportunity in Cambridge, MA from July 13, 2026 – December 11, 2026. Applicants must be available for the entire duration of the Co-op. Start date will be July 13, 2026.

Moderna’s R&D Quality (RDQ) group is seeking a highly motivated college student that has an interest in Quality Assurance in the RDQ environment within the biotech/pharma industry. This position provides an opportunity for inquisitive students who are currently pursuing a Bachelor of Science degree (e.g., Biology, Chemistry, Pharmacy etc.) to get firsthand experience working with a R&D Quality team in a fast-paced environment providing proactive compliance guidance and support across all RDQ GXPs (GCP/GLP/GVP/CSV). The R&D Quality Co-op will also contribute to key development projects and help advance the overall maturity of our program. If you are bold, relentless, collaborative, and obsess over learning, a Co-op program at Moderna can help augment your education and accelerate your career.

The R&D Quality Co-op will support RDQ staff across R&D Quality initiatives, contributing to process enhancement, operational support, and quality system activities. The role will assist with GxP CAPA and Issue Management, support Health Authority inspection readiness activities as needed, and help maintain oversight of audit data and records within the Veeva Audit Management System. The Co-op will also have the opportunity to observe experienced RDQ Auditors conducting audits, as scheduling permits. Success in this position requires strong communication skills and the ability to collaborate effectively in a dynamic, cross-functional matrix environment.

Here’s What You’ll Do

• Contribute and support continuous improvement initiatives in the Quality space (e.g., AI projects) that will focus on evaluating and streamlining audit processes and tools

• Support oversight of data and audit records in the Veeva Audit Management System

• Support CAPA and Issue Management across all GxPs

• Support site selection and audit scheduling

• Train in the conduct of audits (non-travel)

• Aid in the creation of documentation for Moderna conducted audits

• Assist in preparation for Health Authority inspections, as needed

• Contribute to Quality Optimization efforts in training administration, procedural documents, and metrics/reporting

• Learn current regulatory and quality expectations by supporting oversight of audit records and data integrity within the Veeva Audit Management System.

• Learn about Quality study team support

• Accept candid feedback and seek opportunities for self-improvement

• Engage in various departmental activities and attend relevant meetings as required

Here’s What You’ll Need (Basic Qualifications)

• Currently enrolled as a student working towards a bachelor’s degree in a science focused program (e.g., Biology, Chemistry, Pharmacy) or similar

• At least 3 years of study in one of the above scientific fields preferred

• Basic familiarity with pharmaceutical regulations (GCP, GVP, GLP, CSV) is a strong plus

• Excellent organizational skills and ability to manage multiple priorities

• Proficient with Microsoft Office/365 (Excel, Word, PowerPoint)

• 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.

Here’s What You’ll Bring to the Table (Preferred Qualifications)

• Interest and foundational understanding of clinical trial quality concepts such as audit readiness, inspection readiness, and quality risk thinking (coursework/internship/project exposure welcomed)

• Knowledge of ICH-GCP principles and ability to apply them in real-world scenarios (e.g., documentation expectations, traceability, data integrity)

• Comfort working in regulated electronic systems (e.g., Veeva and/or similar QMS/eTMF/document systems) with attention to data accuracy and record completeness

• Strong analytical and reporting skills: ability to build/maintain trackers, use Excel to summarize trends, and communicate insights to stakeholders

• 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 salary range for this role is $20.00 - $60.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. 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.

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 leavesandaccommodations@modernatx.com. 

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.