QC Specialist II – LIMS/Master Data

Role: QC Specialist II focused on LIMS/Master Data management supporting Quality Control in biopharma manufacturing. Objectives: maintain and optimize LabWare LIMS to ensure data integrity, compliance with cGMP, and efficient QC operations. Responsibilities: create, update, and troubleshoot master data in LIMS and Empower CDS; configure sample plans, product data, and workflows; support validation efforts and system enhancements; ensure adherence to data integrity and documentation standards; report technical issues and maintain SOPs. Requirements: Bachelor's in Chemistry, Biology, or related; experience with LabWare LIMS, Empower Master Data, and change management; understanding of data flow and structure within LIMS; knowledge of GMP, data integrity, and Good Documentation Practices. Preferred: 1+ year GMP lab/system infrastructure experience; familiarity with laboratory instrumentation. High-Value: biopharma QC environment, focus on data integrity, cGMP compliance, lab systems validation, and instrument integration. Location: Morrisville, NC; relocation support not provided. Travel: not specified.