Associate Scientist III, Parenteral Drug Product Development

Role: Associate Scientist III in Parenteral Formulation and Drug Product Development, contributing to formulation development and manufacturing process support for Biogen's pipeline. Responsibilities: plan and execute laboratory experiments on formulation characterization, process development, and new technology evaluation; manage development activities independently under senior guidance; prepare and analyze data, author technical reports, and ensure documentation compliance; collaborate with cross-functional teams including Analytical Development, Manufacturing, and Regulatory to support CMC submissions and project goals; contribute to continuous improvement and implementation of new technologies. Qualifications: Bachelor's in Chemistry, Chemical Engineering, Biochemistry, or Pharmaceutical Sciences with 0-2 years, or Master's with 0+ years of industry experience; experience in pharmaceutical/biotech lab environment, familiarity with sterile parenteral formulation, laboratory techniques, and Good Documentation Practices; knowledge of analytical instrumentation and aseptic techniques preferred. HighValue: sterile parenteral drug development, biologics/peptides, formulation characterization, CMC support, GLP compliance, collaboration across R&D and manufacturing teams. WorkSetup: collaborative matrix environment, no specific work location or travel specified.