Principal Scientist, Analytical Development

Role: Lead analytical development for oligonucleotides and bioconjugates, supporting drug substance and drug product characterization from preclinical to commercial stages. Responsibilities: develop, establish, and validate analytical methods (e.g., LC, MS, electrophoresis), ensure cGMP compliance, contribute to control strategies, support regulatory documentation, and collaborate across cross-functional teams. Lead analytical transfer, support manufacturing, and mentor team members. Requirements: BS/BA with 15+ years, MS with 13+ years, or PhD with 7+ years in Analytical Chemistry or related fields; extensive experience with oligos, bioconjugates, biologics, and analytical techniques; thorough knowledge of cGMP and regulatory standards (FDA, EMA, ICH). High-Value: expertise in oligonucleotides/bioconjugates, biologics process development, analytical method validation/qualification, regulatory CMC support, and cross-functional collaboration in biopharma. Work setup: not specified; likely office-based with potential for cross-site interactions.