Associate Quality Control - NS

Target PR Range: 32-42/hr DOE Execute QC activities, working with the day and night shift managers, including sample receipt, prioritization, and accurate entry into LIMS. Perform routine and complex analytical testing in chemistry, bioassay, and/or microbiology, including STAT testing as required. Ensure accurate, compliant documentation in accordance with GDP, GMP, and 21 CFR Part 11 requirements. Support laboratory investigations related to deviations or OOS results and communicate shift-level risks to QC leadership. Utilize electronic systems including LIMS, Biovia (LES, ELN, CIMS/CISPro), and Veeva Vault (QualityDocs, QMS). Collaborate cross-functionally to meet testing timelines and contribute to continuous improvement initiatives. Preferred – Bachelors degree in a scientific discipline or equivalent experience, entry level will be considered. Experience working in a GMP-regulated environment and ability to work independently. #J-18808-Ljbffr Planet Pharma Group