Specialist, Quality Control, Chemistry

• Performing routine analytical chemistry testing such as HPLC, UPLC, UV, particle analysis, and dynamic light scattering.
• Executing and supporting stability studies and GMP release testing.
• Managing LIMS (LabVantage) sample result entries and executing electronic assay forms.
• Assisting with method transfers and development activities across the QC Chemistry function.
• Supporting special projects and ongoing initiatives in QC laboratory optimization and compliance.
• Performing general laboratory operations including sample management, reagent preparation, equipment maintenance, and lab housekeeping.
• Completing and maintaining cGMP documentation and ensuring full data integrity compliance.
• Writing and revising SOPs, protocols, and reports in accordance with internal and external requirements.
• Contributing to the training and troubleshooting activities for more junior staff.
• Participating in investigations, deviations, change controls, and CAPAs within quality systems.
• Supporting the overall lab readiness and supply stocking to ensure uninterrupted QC operations.
• Creating a safe working environment and complying with all GxP and company standards.

• BA/BS in Chemistry (preferred) or other relevant scientific discipline with 2-5 years' experience. A student in an undergraduate program (BA/BS) is acceptable.
• 2-5 years of experience in quality control laboratory of a pharmaceutical company
• Hands on experience with analytical chemistry testing including chromatographic techniques- HPLC, UPLC, Spectroscopic and Spectrometric techniques
• Physical properties techniques such as Particle Analysis by Dynamic Light Scattering and others.
• Working experience in a GMP environment.
• Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred.
• Ability to collaborate effectively in a dynamic, cross-functional matrix environment.
• Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.
• This position is site-based, requiring you to be at Moderna's site full-time.
• Proficiency in English (verbal and/or written) required due to global collaboration needs.

Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred.

• Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
• A holistic approach to well-being with access to fitness, mindfulness, and mental health support
• Family building benefits, including fertility, adoption, and surrogacy support
• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
• Savings and investments to help you plan for the future
• Location-specific perks and extras