Lead Pharmacist: Pharmacy Compliance & Quality Assurance

Alt; Daphne (AL); Hybrid; USD 150,000 - 190,000; Full time

Benefits offered by this job

Medical, Dental & Vision plans

Flexible Spending/Health Savings

Flexible PTO

401(k) + Company Match

Life Insurance & Pet insurance

Job summary

Triad Rx is seeking a Lead Pharmacist, Pharmacy Compliance to act as the on-site compliance authority at its Daphne, AL facility. You will own USP <795> and <800> program execution, ensure audit-ready operations, and serve as the primary interface with centralized leadership.

Responsibilities include managing environmental monitoring, SOP maintenance, training, CAPA, and regulatory communications. A strong background in sterile compounding QA and regulatory readiness is required.

Qualifications

• Active, unrestricted pharmacist license in the state of practice.
• 3+ years in compounding or pharmaceutical QA at a licensed facility.
• Hands-on experience with USP <795> and <800> (2023).
• Experience with deviation investigations, CAPA, or regulatory data analysis.

Responsibilities

• Own day-to-day USP <795>/<800> compliance and keep operations auditable.
• Manage environmental monitoring: air sampling, particle tracking, and instrument calibration.
• Maintain SOP library with updates and training.
• Lead personnel training and competency assessments per USP <795>.
• Own CAPA program: deviation handling, root cause analysis, corrective actions, and trend reporting.

Skills

Regulatory compliance

USP <795>/<800> knowledge

Quality systems

Environmental monitoring

CAPA management

Education

B.S. in Pharmacy or Pharm.D.

Tools

CAPA systems

EM programs

Job description

Triad Rx is seeking a Lead Pharmacist, Pharmacy Compliance to act as the on-site compliance authority at its Daphne, AL facility. You will own USP <795> and <800> program execution, ensure audit-ready operations, and serve as the primary interface with centralized leadership.

Responsibilities include managing environmental monitoring, SOP maintenance, training, CAPA, and regulatory communications. A strong background in sterile compounding QA and regulatory readiness is required.