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OH
OpenLoop Health
Lead Pharmacist, Pharmacy Compliance
Career Insights for Compounding Pharmacist
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Based on Alabama data
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What they do
A Compounding Pharmacist provides medications to patients and educates patients and physicians on the proper use of medications. Works for a compounding pharmacies. Specializes in preparation of alternate modes of delivery and forms of commercial medication not available in retail or hospital pharmacies.
$132,406 / year median in Alabama
+3% projected growth
Job Description
About OpenLoop OpenLoop was co-founded by CEO, Dr. Jon Lensing, and COO, Christian Williams, with the vision to bring care anywhere. Our telehealth support solutions are thoughtfully designed to streamline and simplify go-to-market care delivery for companies offering meaningful virtual support to patients across an expansive array of specialties, in all 50 states. About the Role Triad Rx is looking for a Lead Pharmacist, Pharmacy Compliance to serve as the on-site compliance authority at its non-sterile licensed compounding facility— owning USP , and program execution, maintaining inspection readiness, and acting as the primary compliance interface between the site and centralized pharmacy leadership. This role reports directly to the corporate compliance leadership team. What You'll Do Own day-to-day USP and (2023) compliance — keeping operations, controls, personnel practices, and quality systems current, documented, and audit-ready.
D. from an ACPE-accredited institution with an active, unrestricted pharmacist license in the state of practice. Additional state pharmacist licensure is beneficial, but not required 3+ years of hands-on experience in sterile compounding operations or pharmaceutical QA at a licensed 503A facility or 5+ years in pharmaceutical quality/compliance without direct 503A experience, with commitment to complete USP training in 90 days. Practical command of USP and (2023) — EM programs, competency requirements, and quality systems. Experienced with deviation investigations, CAPA, and environmental monitoring data analysis. Disciplined documenter, risk-based thinker, and self-directed — able to manage competing compliance obligations without close oversight. Collaborative communicator who can translate regulatory requirements into clear operational direction for staff and escalate clearly to leadership. Required Qualifications Active, unrestricted pharmacist license in the state of practice. B.S. in Pharmacy or Pharm.
D. from an ACPE-accredited institution. 3+ years in compounding pharmacy operations or pharmaceutical QA at a licensed 503A facility. Working knowledge of USP and (2023). Hands-on experience with EM programs, deviation management, or CAPA systems. Preferred Qualifications Experience at a state-licensed 503A sterile compounding pharmacy. Familiarity with state board inspection processes and sterile compounding enforcement.
Manage the environmental monitoring program:
viable air sampling, non-viable particle and pressure/temperature/humidity tracking, action level investigation, and CAPA. Maintain the SOP library — draft, update, version-control, and train personnel on all compliance-related procedures. Run the personnel training and competency program perUSP :
initial and ongoing assessments and remediation. Own the site CAPA program — deviation documentation, root cause analysis, corrective action tracking to verified closure, and trend reporting to leadership.Maintain facility qualification records:
Hazardous room certification schedules, equipment re-qualification triggers, and calibration documentation.Coordinate USP compliance:
engineering controls, PPE protocols, Assessment of Risk, and spill response readiness. Oversee MFR/CR completeness, BUD documentation, incoming material/COA review, and supplier qualification records. Conduct mock inspections and gap assessments; support response to state board, FDA, or accreditation survey findings. Manage product complaints, adverse event reporting, and site-level recall procedures. Other duties as assigned. Who You Are B.S. in Pharmacy or Pharm.D. from an ACPE-accredited institution with an active, unrestricted pharmacist license in the state of practice. Additional state pharmacist licensure is beneficial, but not required 3+ years of hands-on experience in sterile compounding operations or pharmaceutical QA at a licensed 503A facility or 5+ years in pharmaceutical quality/compliance without direct 503A experience, with commitment to complete USP training in 90 days. Practical command of USP and (2023) — EM programs, competency requirements, and quality systems. Experienced with deviation investigations, CAPA, and environmental monitoring data analysis. Disciplined documenter, risk-based thinker, and self-directed — able to manage competing compliance obligations without close oversight. Collaborative communicator who can translate regulatory requirements into clear operational direction for staff and escalate clearly to leadership. Required Qualifications Active, unrestricted pharmacist license in the state of practice. B.S. in Pharmacy or Pharm.
D. from an ACPE-accredited institution. 3+ years in compounding pharmacy operations or pharmaceutical QA at a licensed 503A facility. Working knowledge of USP and (2023). Hands-on experience with EM programs, deviation management, or CAPA systems. Preferred Qualifications Experience at a state-licensed 503A sterile compounding pharmacy. Familiarity with state board inspection processes and sterile compounding enforcement.