Associate II, Quality Control

Role: Associate II in cGMP quality control analytical testing within Moderna's biopharmaceutical lab, supporting drug substance, intermediates, and drug products. Objectives: perform in-process, release, and stability testing to ensure compliance with regulatory standards. Responsibilities: conduct analytical assays using equipment like HPLC, UPLC, UV, DLS, and KF; document results per cGMP and FDA/ICH guidelines; support investigations of OOS/OOT deviations; assist with SOP and protocol writing, reagent management, and lab housekeeping. Qualifications: BA/BS in Chemistry or related field; minimum two years' QC lab experience in pharma; proficiency in analytical techniques and data integrity. Preferred: familiarity with cGMP, lab troubleshooting, and investigation procedures. High-Value Details: role is 100% onsite, emphasizing hands-on collaboration; supports quality testing critical to mRNA vaccine production; involved in regulatory compliance and laboratory investigations. Collaboration: work closely with QC team and other lab personnel. Work Setup: onsite only, no travel specified.