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sop development usp 795 non-sterile compounding sterile compounding usp 800π Description
- Oversee sterile and non-sterile compounding processes.
- Prepare, dispense, and label compounded medications.
- Lead sterile compounding in compliance with USP 797.
- Maintain documentation for all compounding activities (batch sheets, logs, compliance checks).
- Conduct product and batch verification to ensure quality and patient safety.
- Develop and implement SOPs for sterile compounding; train staff.
π― Requirements
- Active Florida Pharmacist license (required).
- β₯2 years sterile compounding; non-sterile preferred.
- Supervisory experience in a compounding setting preferred.
- Knowledge of USP 795/797/800 guidelines.
- Experience with GLP-1 medications (semaglutide, tirzepatide) preferred.
- Strong QA, documentation, and regulatory compliance skills.
π Benefits
- 12 days PTO plus 6 paid holidays.
- Paid sick leave and floating holidays.
- Private medical insurance via UnitedHealthcare.
- Dental and vision coverage.
- 3% employer 401(k) match.
- Headspace subscription with family option.
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