Quality Control Analyst I

Role: Laboratory analyst responsible for routine and non-routine chemical testing of pharmaceutical products in a cGMP environment. Objectives: ensure analytical testing compliance, data accuracy, and support quality control operations. Responsibilities: perform analyses using HPLC, GC, UV/Vis, KF, FTIR; utilize LIMS and Empower systems; review data, troubleshoot methods/instruments, and participate in investigations; maintain documentation and equipment; promote quality standards and continuous improvement; collaborate within the team and communicate findings. Requirements: Bachelor's degree in science (preferably Chemistry); experience in a cGMP laboratory. Preferred: familiarity with USP, FDA, and GLP regulations; knowledge of pharmaceutical analytical methods. High-Value: experience in pharmaceutical quality control, analytical chemistry, and GxP compliance; focus on chemical testing of commercial, validation, and stability samples; ability to work independently and collaboratively. WorkSetup: not specified; likely onsite or hybrid given lab environment.