Associate III, Quality Control Chemistry

Role: Support QC Chemistry in ensuring compliance with cGMP standards, focusing on release/stability testing, investigations, and data integrity within a biopharma laboratory setting. Responsibilities: perform release and stability assays, review data and documentation, author or review protocols and reports, support analytical method transfer, qualification, and validation projects, and provide technical leadership and mentorship. Requirements: Bachelor's or Associate's degree in biological/chemistry/life sciences with 2+ years lab experience; HPLC expertise; knowledge of QC Chemistry methodologies and FDA/EMEA regulations. Preferred: GMP experience, LC MS, Dissolution, Karl Fischer, GC skills, and experience with small molecules or antisense oligonucleotides. High-Value: QC Chemistry, cGMP compliance, HPLC, small molecules, IND/clinical manufacturing stages, technical leadership, cross-departmental collaboration. Work setup: not specified.