Pharmacy Technician, Sterile Compounding 503A (2nd Shift)

Empower Pharmacy is a visionary healthcare company dedicated to making quality, affordable medication accessible to millions of patients nationwide. As the most advanced 503A compounding pharmacy and FDA-registered 503B outsourcing facility serving the functional medicine markets, we are proud to be recognized as one of Houston’s fastest-growing private companies and ranked #116 in Healthcare &amp; Medical on the Inc. 5000 List for 2025. Our strength lies in four core values—People, Quality, Service, and Innovation. Guided by these principles, we deliver a uniquely integrated approach to healthcare through vertical supply chain integration, advanced technology, and a relentless pursuit of excellence. From manufacturing to distribution to quality control, our teams work collaboratively to push boundaries, improve patient outcomes, and redefine medication accessibility. At Empower, joining our team means more than starting a new job, it means becoming part of a mission to transform healthcare. We empower our employees to innovate, grow, and make a meaningful impact every day. Here, your ideas are valued, your growth is supported, and your contributions are celebrated. If you thrive in a fast-paced, transformative environment where innovation meets purpose, Empower Pharmacy is the place for you. Let’s revolutionize healthcare together. Position Summary: The Pharmacy Technician, Sterile Compounding supports high-impact sterile compounding operations that enable safe, scalable medication production within Empower’s 503A/503B environment. This role owns end-to-end execution of aseptic preparation, documentation, and cleanroom readiness while ensuring regulatory compliance and batch quality. The Technician operates within cGMP and USP 797/800 standards, contributing to operational excellence, patient safety, increased capacity, reduced variability, and strong compliance practices. Responsibilities: Sterile Operations Aseptic Execution: Perform sterile compounding using validated aseptic techniques within ISO-classified cleanrooms. Process Compliance: Execute compounding processes in strict adherence to batch records, SOPs, USP 797/800, cGMP, and regulatory requirements. Equipment Operation: Operate and monitor compounding and sterilization equipment to support reliable production flow and minimize downtime. Quality and Compliance Documentation Accuracy: Complete compounding documentation and batch records with precision, ensuring traceability, compliance, and inspection readiness. Deviation Response: Identify, escalate, and support investigation of deviations using structured problem-solving and root cause analysis. Inspection Readiness: Maintain readiness for internal and external audits by adhering to protocols and supporting documentation reviews. Cleanroom and Efficiency Environment Control: Maintain cleanroom integrity through cleaning, sterilization, and environmental monitoring. Workflow Optimization: Apply LEAN principles, including 5S and root cause analysis, to streamline workflows, reduce waste, and improve cycle times. Team Collaboration:</str