Key Responsibilities (including but not limited to): Perform routine and non-routine analytical, preferably HPLC/UPLC and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs. Qualifications: B.S. in chemistry, biology, or biochemistry, or related scientific field; Pharmaceutical/Biotech industry experience with 4-8 years in a GMP Quality Control function or equivalent, relevant industry experience.