- Lead and oversee day-to-day sterile compounding operations in accordance with USP <797> and <800> standards.
- Assist in the design, setup, and validation of a new compounding lab facility, including layout planning, equipment procurement, and regulatory readiness.
- Hire, train, and manage pharmacy staff to ensure adherence to protocols and continuous improvement in quality and productivity.
- Maintain full compliance with state and federal regulations, accreditation requirements, and internal SOPs.
- Collaborate with cross-functional departments to ensure seamless operations from formulation to final product release.
- Implement and oversee quality assurance programs and risk management strategies.
- Serve as the Pharmacist-in-Charge (PIC) if designated.
- Monitor and manage inventory, ordering, and proper storage of pharmaceutical products and supplies.
- Stay current with industry regulations, best practices, and innovations in compounding pharmacy.
- Doctor of Pharmacy (PharmD) or BS in Pharmacy from an accredited institution.
- Active and unrestricted Texas Pharmacist License in good standing.
- Minimum 5 years of experience in sterile compounding, including aseptic techniques and hazardous drug handling.
- At least 3 years of experience in a pharmacy management or leadership role.
- Experience building and launching a sterile compounding lab or pharmacy from the ground up is required.
- Strong knowledge of USP <797>, <800>, and FDA 503A/503B guidelines.
- Excellent leadership, problem-solving, and communication skills.
- Ability to thrive in a fast-paced, startup-like environment with high standards and expectations.
- Experience in a 503A or 503B facility.
- Lean or Six Sigma certification is a plus.
- Familiarity with pharmacy software systems and sterile compounding documentation platforms.