2026 Co-op, Good Laboratory Practice / Good Clinical Practice
About The Position
This is a fall Co-op opportunity in Norwood, 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 Laboratory Quality in the RDQ environment within the biotech/pharma industry. This position provides an opportunity for inquisitive students who are currently pursuing a degree in Life Sciences, Health and Human Services or related fields to get firsthand experience working with the RDQ Laboratory Quality team in a fast-paced environment providing proactive compliance guidance and support across all RDQ GXPs (GLP/GCP). The RDQ Co-op will support Moderna’s R&D laboratory operations by assisting with day-to-day quality activities and gaining knowledge with applicable internal procedures, regulatory requirements and guidance (e.g., GLP/GCLP, internal policies). Key contributions include defining and monitoring compliance KPIs, trending and reporting quality metrics to drive continuous improvement, and assisting in the creation and maintenance of quality processes and procedures (SOPs, work instructions, and templates). The role will also support the review of assay method validation documentation and results for clinical sample analysis within study-specific regulated processes, as well as provide support for internal and external audits of laboratory deliverables.
Requirements
- 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, as well as 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
- This position is site-based, requiring you to be at Moderna’s site full-time.
- This position is not eligible for remote work.
- Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.
Nice To Haves
- Bioanalytical technology knowledge, including, but not limited to LIMS, ELISA, Functional Assays, PCR, plate readers, and mass spectroscopy proficiency is highly desired
- Critical thinking and problem-solving skills
- Working knowledge in any of the following areas desired: 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
- A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.
Responsibilities
- Support QA audits of laboratory deliverables, gaining firsthand experience with GLP and GCP.
- Assist in 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.
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Intern
