Co-Op, Bioanalytics
About The Position
This is a co-op opportunity based in Norwood, MA from January 18, 2027 – June 25, 2027. Applicants must be available for the full duration of the co-op term. Occasional travel to Moderna’s Cambridge, MA site will be required. Start date will be January 18, 2027. Bioanalytical and Molecular Assay (BMA) laboratories at Moderna is seeking a motivated Co-op to support Data Quality Control activities. In this role, you will gain hands-on experience in a regulated laboratory environment supporting preclinical and clinical development programs. You will work closely with QC and laboratory scientists to review bioanalytical and molecular assay data, support data integrity and compliance efforts, and contribute to initiatives that strengthen quality standards across GLP/GcLP studies. This position offers valuable exposure to quality systems, regulated data review, and cross-functional collaboration within a fast-paced biotechnology environment.
Requirements
- Current student enrolled in a Bachelor’s or Master’s program in Chemical Engineering, Biochemical Engineering, Bioengineering, Biomolecular Engineering, Chemistry, Biochemistry, Biomedical Engineering, Biophysics, Biostatistics, Biotechnology, Mathematics, Molecular Biology, Pharmaceutical Science, Statistics, or a related field
- Strong fundamental scientific and engineering skills for the evaluation of experimental data
- Laboratory skills applicable to bioprocess development and analytical methods
Nice To Haves
- GPA of 3.5 on a 4 scale or equivalent
- Demonstrated ability to work both independently as well as the ability to contribute to high performing teams.
- Excellent written and verbal communication skills.
- A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.
Responsibilities
- Assist in QC review of bioanalytical and molecular assay data generated through LC-MS, LBA, and molecular platforms (e.g., RT-qPCR).
- Support review of raw data and source documentation, including: ELN entries, LIMS (e.g., Watson) entries, Equipment records, Analytical batch records.
- Help verify data accuracy, completeness, and compliance with GLP/GcLP/SOP requirements.
- Support reconciliation of QC/STD runs and review of tables and summary outputs.
- Assist in compiling quality metrics and tracking data trends using tools such as Excel and JMP.
- Participate in review of protocols, methods, and reports to ensure documentation consistency and quality.
- Support document management activities in systems such as Veeva.
- Collaborate with laboratory scientists and cross-functional teams to resolve data queries.
- Assist in maintaining organized QC documentation and tracking logs.
- Contribute to continuous improvement initiatives related to data quality and process efficiency.
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
Career Level
Intern
Education Level
No Education Listed
