2026 Co-op, Good Laboratory Practice / Good Clinical Practice

Support QA audits of laboratory deliverables, gaining firsthand experience with GLP and GCP.,Assist in the review of validation and lifecycle management compliance to meet internal standards.,Collaborate with team members to develop and maintain laboratory systems compliant with regulations and guidelines.,Contribute to risk impact assessments and evaluate potential risks.,Overview of audit study materials and reports for nonclinical, biomarker, and bioanalytical studies.,Assist audit team with audit deliverables, CAPAs, and responses.,Trending of metrics and KPIs related to department activities.

Currently pursuing a degree in Life Sciences, Health and Human Services, or related field.,Basic understanding of GLP and GCP requirements, lifecycle controls, and the drug development process.,Basic understanding of Quality Assurance (QA), clinical development, and clinical sample analysis.,Basic familiarity with pharmaceutical regulations (GLP/GCP) is a strong plus.,Prior experience or coursework in Quality Assurance is a plus.,Proficient with Microsoft Office/365.,Must already hold work authorization in the US and be able to maintain that status without the need for future sponsorship.,Bioanalytical technology knowledge, including LIMS, ELISA, Functional Assays, PCR, plate readers, and mass spectroscopy proficiency is highly desired.,Critical thinking and problem-solving skills.,Working knowledge in cell/tissue culture, in vitro transfections, protein/antibody detection methods (e.g., MSD, ELISA, Luminex), molecular biology techniques (e.g., PCR, DNA/RNA extractions), assay development, and troubleshooting.,Prior Co-op or internship experience is preferred but not required.

Degree in progress (Life Sciences, Health and Human Services, or related field)

Must be available for the entire duration of the Co-op (July 13, 2026 – December 11, 2026).,Must already hold work authorization in the US and be able to maintain that status without the need for future sponsorship.,Position may involve access to technology or data subject to U.S. export control laws (EAR).,Only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible due to export control regulations.,Moderna is unable to sponsor non-U.S. persons for an export control license.