Compounding Pharmacist
- Compensation
- Not disclosed
- Location
- Houston, Texas
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Not specified
- Experience
- Not specified
- Category
- Healthcare
- Posted
Skills
Nice to have
- Experience as a Designated Person, PIC, or in a QA/QC role at a compounding facilitycGMP experience in an FDA-registered 503B outsourcing facilityExperience scaling compounding operations, validating
- Physical Requirements
- Periods of standing; ability to work in a cleanroom in full garb as neededPotential exposure to hazardous drugs with appropriate controlsAbility to lift up to 25lbs
- All Company policies and procedures are subject to change without notice based on business needs. This includes, but is not limited to, the locations where we hire remote, hybrid, or onsite employees.
- U.S. Applicants Only Don’t meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Remedy we a
Full description
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! Compounding Pharmacist
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.
Comp | Perks | Benefits
- 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.
What you get to do every day
Verification & Clinical Oversight
Perform final verification of all CSPs and non-sterile preparations, including ingredient identity, calculations, technique observation, labeling, and physical inspectionReview and approve compounding records prior to releaseConduct prospective review of prescriptions for appropriateness, dose, route, compatibility, stability, and drug interactionsConfirm patient-specific prescriptions are valid and, where applicable, that compounding is permitted for the drug and dosage formServe as the clinical resource for prescribers and patients on formulation, stability, storage, and administration
Formulation & Quality Systems
Develop, review, and approve master formulation records with documented, defensible stability and beyond-use dating rationaleEstablish BUDs based on published stability data, USP defaults, or facility-specific stability studies — not assumptionCoordinate sterility, endotoxin, potency, and container-closure integrity testing; review and act on resultsInvestigate deviations, OOS results, complaints, and adverse events; document root cause and CAPAAuthor and maintain SOPs; ensure revisions are controlled, trained, and effective-dated
Compliance & Facility Oversight
Support or serve as the Designated Person under USP <797>/<800>, as assignedOversee environmental monitoring programs and trend results; escalate excursionsVerify equipment certification, calibration, and PEC/SEC recertification schedulesMaintain the hazardous drug assessment of risk and associated controlsPrepare for and support Board of Pharmacy, FDA, and accreditation inspectionsEnsure compliance with DQSA Section 503A / 503B requirements, including prescription-based dispensing / cGMP obligations