2026 Co-Op, R&D Quality

Moderna Theraputics•Massachusetts, MA

77d•Onsite

About The Position

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. Our Spring co-op program will run from January 19 - June 26, 2026. All applicants must be available to work full-time and on site (Cambridge, MA) for the entire duration of the program. The R&D Quality Co-Op role will focus on assisting RDQ staff with continuous improvement initiatives in the Clinical Quality space. This position will also assist with GCP CAPA and Issue Management, support Health Authority inspections as needed, and will help support oversight of data and records in the Veeva Audit Management System. The Co-Op program will also provide the opportunity for the Co-Op to observe experienced RDQ Auditors in conducting clinical audits. The candidate must also possess the ability to effectively interact and collaborate in a dynamic, cross-functional matrix environment.

Requirements

Currently enrolled as a student working towards a bachelor's degree in a science focused program (i.e., 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
Must possess excellent organization skills and ability to manage multiple priorities
Basic familiarity with Microsoft Excel, Word, PowerPoint, etc. is a plus
Excellent verbal and written communication skills and the ability to interact professionally with a diverse group, executives, managers, and subject matter experts
Willingness to learn, be mentored, and improve
Ability to work independently and in collaborative team environments
Ability to work in a fast-paced demanding environment
Ability to prioritize based on shifting demands
Ability to multitask and know when to ask for help
Willing and able to relocate to Cambridge, MA for the co-op
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.

Nice To Haves

Basic familiarity with pharmaceutical regulations (GCP, GVP, GLP, CSV) is a strong plus
Basic familiarity with Microsoft Excel, Word, PowerPoint, etc. is a plus

Responsibilities

Contribute and support continuous improvement initiatives in the Clinical Quality space (e.g., AI projects) that will focus on evaluating and streamlining GCP audit processes and tools
Support oversight of data and audit records in the Veeva Audit Management System
Support GCP CAPA and Issue Management
Support site selection and audit scheduling
Train in the conduct of clinical (GCP) 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 about current regulatory requirements by contributing to the development of quarterly newsletter and regulatory intelligence activities
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