Quality Control Associate

Seeking a detail-oriented Associate II, Analytical Development/Quality Control professional to support analytical testing, method development, and quality control activities within a regulated pharmaceutical or biotech environment. This role is responsible for executing analytical assays, maintaining data integrity, supporting investigations, and collaborating cross-functionally to ensure product quality and compliance with cGMP standards. Responsibilities Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products. Support Environmental Monitoring activities and laboratory operations. Execute analytical assays using techniques such as HPLC/UPLC, GC, UV-Vis, and microscopy. Record, review, and maintain accurate laboratory data and documentation in compliance with GMP and GDP requirements. Assist with investigations related to out-of-specification (OOS) results and deviations. Support analytical method development, optimization, qualification, and transfer activities. Prepare technical documents including protocols, reports, and data summaries. Perform data review, trending, and quality assessments. Collaborate with Manufacturing, Quality Assurance, and Project Management teams to support project and client needs. Communicate testing results, observations, and issues clearly to stakeholders. Qualifications Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field. 0–3+ years of experience in pharmaceutical, biotech, or CDMO environments. Hands-on experience with analytical techniques, including HPLC/UPLC preferred. Understanding of cGMP, GDP, and laboratory compliance standards. Strong documentation, organizational, and data integrity skills. Ability to manage multiple priorities in a fast-paced, client-driven environment. #J-18808-Ljbffr