Scientist II, Analytical Development

Role: Analytical Development Scientist II supporting method development, validation, and routine testing for clinical-stage inhaled therapeutics in a biopharma setting. Responsibilities: design and execute experiments using techniques like HPLC, UV, GC; analyze data; maintain documentation per GLP/GMP; troubleshoot analytical issues; collaborate cross-functionally with formulation, process development, and quality teams; contribute to process improvements and ensure compliance. Qualifications: MS in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or related; 1–3 years (MS) or 2–4 years (B.S.) of relevant experience; hands-on with analytical instruments; familiar with ICH, GMP/GLP; detail-oriented with strong organizational skills. Preferred: experience supporting clinical development, method validation, electronic lab notebooks, and working with small molecules in regulated environments. Core competencies include adherence to quality standards, collaboration, ownership, persistence, and innovation. Work setup details and additional qualifications not specified.