Specialist, Quality Control
Moderna
September 22, 2026
Full-time
On-site
Norwood, MA
Operations
Role: Quality Control Chemistry Specialist responsible for analytical testing, data review, and report generation for clinical and commercial Moderna products. Responsibilities include performing routine analyses (HPLC, GC, UV, Particle Analysis, DLS), supporting method validation, troubleshooting, data trending, and documentation in compliance with cGMP and GxP standards. The role also involves supporting stability programs, sample management, equipment maintenance, and authoring relevant procedures and reports. Requirements: Bachelorโs in Analytical Chemistry, Chemistry, or related field; minimum 5 years laboratory experience in analytical chemistry; familiarity with GxP regulations. Preferred skills include experience with QC testing for biologics or mRNA-based products, proficiency with LIMS, and shift flexibility to support STAT testing. High-value specifics include a focus on biologics/clinical-stage products, cGMP environment, and laboratory support for manufacturing. The position is 100% onsite at Norwood, MA, with no mention of travel. This role supports Modernaโs mission in mRNA therapeutics and involves collaboration with QC and manufacturing teams to ensure product quality and compliance.