Loading jobs…
Loading jobs…
Carma — Houston, Texas
Empower Pharmacy is a visionary healthcare company dedicated to making quality, affordable medication accessible to millions of patients nationwide. As the nation’s most advanced 503A compounding pharmacy and FDA-registered 503B outsourcing facility, we’re redefining what’s possible in personalized medicine and pharmaceutical manufacturing. We’re proud to be recognized as one of Houston’s fastest-growing private companies and ranked #116 in Healthcare Medical on the Inc.
5000 List for 2025. Our strength is built on four core values: People, Quality, Service, and Innovation. Guided by these principles, we’ve created a uniquely integrated healthcare platform powered by advanced technology, operational excellence, and a relentless commitment to patient care.
From manufacturing and quality control to distribution and customer experience, our teams work together to raise industry standards, expand access to critical medications, and improve outcomes for patients and providers across the country. At Empower, joining our team means more than starting a new role. It means becoming part of a mission-driven organization that’s transforming healthcare at scale.
We invest deeply in our people, encourage bold thinking, and create opportunities for growth, leadership, and innovation at every level. Your ideas matter here, your development is supported, and the work you do has a direct impact on the lives of millions. If you thrive in a fast-moving, purpose-driven environment where innovation, collaboration, and ambition come together, Empower Pharmacy is the place for you.
Let’s transform healthcare together. Position Summary This role delivers high-impact sterile compounding execution supporting patient-critical therapies within Empower’s hyper-growth 503A/503B pharmacy environment. The technician owns precise preparation, documentation, and compliance for sterile products, ensuring safety, quality, and throughput.
Leveraging AI-enabled systems to enhance accuracy, speed, and deviation detection, this position operates at the intersection of quality and efficiency. Success requires P80–P90 talent demonstrating disciplined execution, learning agility, and accountability under strict regulatory standards. This role directly influences product integrity, audit readiness, and scalable operations while continuously improving processes, maintaining compliance, and supporting production targets in a highly controlled environment.
Responsibilities
Sterile Operations Aseptic Execution: Perform sterile compounding using aseptic techniques within ISO-classified cleanrooms, ensuring accuracy, contamination control, and adherence to SOPs while consistently meeting production targets and quality standards.
Requirements
Equipment Handling: Operate, clean, and maintain compounding equipment and cleanroom environments, ensuring readiness, proper calibration, and compliance with environmental monitoring and safety protocols at all times. Quality Compliance Documentation Accuracy: Complete batch records, logs, and documentation with precision, ensuring real-time accuracy, traceability, and audit readiness aligned with USP standards and regulatory expectations. Regulatory Adherence: Follow USP 797 , 800 , and internal SOPs rigorously, maintaining strict compliance in all compounding activities while proactively identifying and escalating deviations or risks.
Inspection Readiness: Maintain continuous audit readiness by adhering to GMP standards, supporting inspections, and ensuring all processes, documentation, and environments meet regulatory expectations without exception.