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Specialist, Quality Control

Moderna
September 22, 2026
Full-time
On-site
Norwood, MA
Operations
Role: Quality Control Chemistry Specialist focused on analytical testing for clinical and commercial mRNA products at Moderna's Norwood, MA site. Responsibilities: perform routine QC analyses (HPLC, GC, UV, particle analysis), support method qualification, troubleshoot equipment, enter data, support stability programs, and maintain cGMP documentation. Collaborate on laboratory procedures, support electronic assay execution, and assist in deviations and change controls. Requirements: Bachelor’s in Chemistry or related field, 5+ years in a laboratory setting with analytical chemistry expertise, and knowledge of GxP regulations, especially GMP. Preferred: experience in biopharma QC labs, familiarity with LIMS, troubleshooting skills, and shift flexibility for STAT testing. High-Value: expertise in analytical chemistry for biologics, supporting regulatory compliance, and working within cGMP environments. Work Setup: 100% onsite at Norwood, MA, with potential shift flexibility. The role emphasizes precise documentation, adherence to regulations, and collaboration within a highly regulated biopharma environment.