Compounding Pharmacist

Remedy•Houston, TX

22h

About The Position

Thirty Madison is now part of Remedy! We are excited to join forces and continue to revolutionize healthcare accessibility! As a Compounding Pharmacist, you will provide final verification and clinical oversight of compounded sterile and non-sterile preparations, ensuring every preparation meets standards for identity, strength, quality, and purity. Beyond dispensing accuracy, you will own the quality systems that make compounding defensible: formulation records, competency assessment, deviation investigation, and regulatory compliance under USP <795>, <797>, <800>, and applicable state and federal law.

Requirements

Active pharmacist license in Texas, in good standing; eligible for licensure in additional states as required
5+ years of pharmacy practice with demonstrable sterile compounding experience
Documented aseptic technique training and current qualification
Board certification (BCSCP) or equivalent
Thorough working knowledge of USP <795>, <797>, <800>, and <1163>

Nice To Haves

Experience as a Designated Person, PIC, or in a QA/QC role at a compounding facility
cGMP experience in an FDA-registered 503B outsourcing facility
Experience scaling compounding operations, validating new formulations, or supporting facility buildout
Multi-state licensure

Responsibilities

Perform final verification of all CSPs and non-sterile preparations, including ingredient identity, calculations, technique observation, labeling, and physical inspection
Review and approve compounding records prior to release
Conduct prospective review of prescriptions for appropriateness, dose, route, compatibility, stability, and drug interactions
Confirm patient-specific prescriptions are valid and, where applicable, that compounding is permitted for the drug and dosage form
Serve as the clinical resource for prescribers and patients on formulation, stability, storage, and administration
Develop, review, and approve master formulation records with documented, defensible stability and beyond-use dating rationale
Establish BUDs based on published stability data, USP defaults, or facility-specific stability studies — not assumption
Coordinate sterility, endotoxin, potency, and container-closure integrity testing; review and act on results
Investigate deviations, OOS results, complaints, and adverse events; document root cause and CAPA
Author and maintain SOPs; ensure revisions are controlled, trained, and effective-dated
Support or serve as the Designated Person under USP <797>/<800>, as assigned
Oversee environmental monitoring programs and trend results; escalate excursions
Verify equipment certification, calibration, and PEC/SEC recertification schedules
Maintain the hazardous drug assessment of risk and associated controls
Prepare for and support Board of Pharmacy, FDA, and accreditation inspections
Ensure compliance with DQSA Section 503A / 503B requirements, including prescription-based dispensing / cGMP obligations