Compounding Pharmacist

Thirty Madison is now part of Remedy ! You can read more about the acquisition here . 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 , , , and applicable state and federal law.

• The base pay range for this position is $133,000 - $137,000 per year**
• Robust and affordable Medical, Dental, and Vision plan options
• Flexible time off policy

** Base pay offered may vary depending on job-related knowledge, skills, and experience. An annual incentive plan and stock options may be provided as part of the compensation package, in addition to a full range of medical, financial, and/or other benefits, dependent on the position offered.**

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 CAPAAuthor and maintain SOPs; ensure revisions are controlled, trained, and effective-dated

Support or serve as the Designated Person under USP /, as assigned

Oversee environmental monitoring programs and trend results; elevate 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

Active pharmacist license in Texas, in good standing; eligible for licensure in additional states as required5+ 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 , , , and Sound judgment and the willingness to hold a release when documentation or quality is in question

Experience as a Designated Person, PIC, or in a QA/QC role at a compounding facilitycGMP experience in an FDA-registered 503B outsourcing facility

Experience scaling compounding operations, validating new formulations, or supporting facility buildout

Multi-state licensure

Periods of standing; ability to work in a cleanroom in full garb as needed

Potential exposure to hazardous drugs with appropriate controls

Ability to lift up to…