You will work across APLs, Analytical Development subject matter experts, Analytical Sciences, Product Characterization, Clinical Stability, Process and Product Development, AS&T, QC, Quality, Quantitative Sciences, and Regulatory CMC to translate complex analytical information into accurate, traceable, decision-ready and filing-ready content. with 8+ years of relevant biotechnology or pharmaceutical industry experience in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Chemistry, Biology, Chemical Engineering, or a related scientific discipline, with experience in Analytical Development, CMC, Quality, Regulatory support, or a related technical development function.