Principal Research Associate, Analytical Development

Role: Principal Research Associate focused on analytical development, method transfer, and routine operations for clinical-stage biologics. Responsibilities: serve as liaison among Method Development, Analytical Sciences & Technology, QC, ATO, and QA; ensure analytical methods (e.g., HPLC, molecular biology assays) meet technical, operational, and regulatory standards; troubleshoot assay issues; support investigations, CAPAs, and change controls; author and review technical documentation; drive continuous improvement and method lifecycle management. Requirements: MS with 5+ years or BS with 8+ years in biotech/pharma industry; hands-on expertise in analytical methods; experience with method transfer to QC/external labs; proven troubleshooting skills in GMP or late-stage development; strong data interpretation, cross-functional collaboration, and communication skills; ability to operate in a fast-paced, site-based environment. High-Value: biologics, clinical-stage, GMP, regulatory compliance, analytical methods, troubleshooting, cross-functional interface with Quality, QC, and Manufacturing. Work setup: full-time onsite at Moderna’s site; no remote work; US work authorization required.