The Full-Time Pharmacist supports Medivant's sterile injectable manufacturing operations by ensuring all compounding, labeling, and documentation processes comply with FDA regulations, USP <797>/<800>, and internal SOPs.
This role involves verifying batch records, supervising compounding operations, ensuring quality assurance compliance, and overseeing controlled substance handling as required.
This is a full-time position offering long-term career growth, stability, and the opportunity to work in a highly regulated cGMP manufacturing environment.
Key Responsibilities
Review and approve batch production records, labels, and associated documentation
Supervise sterile compounding and aseptic filling operations to ensure compliance with USP <797>/<800> standards
Verify and document calculations for compounding and formulation accuracy
Monitor cleanroom operations, gowning compliance, and aseptic techniques
Support internal and regulatory audits, CAPA investigations, and validation activities
Ensure compliance with DEA, FDA, and state pharmacy board regulations
Collaborate with Quality Assurance and Production teams to maintain continuous compliance
Provide guidance to technicians and operators on cGMP and pharmacy standards
Participate in review of deviations, investigations, and process improvements
Qualifications
Required:
Active Pharmacist License in the state of Arizona (in good standing)
Minimum 2-3 years of experience in sterile compounding, manufacturing pharmacy, or 503B facility
Strong understanding of USP <797>, USP <800>, cGMP, and FDA manufacturing guidelines
Strong documentation, verification, and analytical skills
Excellent communication and teamwork abilities
Preferred:
Experience in sterile injectable production or pharmaceutical quality assurance
Familiarity with LIMS, ERP, or electronic batch record systems
Prior experience in a 503B outsourcing facility or hospital cleanroom setting
Compensation & Benefits
Competitive base salary (based on experience)
Health, dental, and vision insurance
Paid time off (PTO) and holidays
Opportunities for career growth and advancement
Stable, long-term employment with a growing organization
Numbers & Facts
Location
Chandler, AZ
Skills
Analysis Skillsunmatched
Asepsisunmatched
Biotech and Pharmaceuticalunmatched
Cleanroomunmatched
Communication Skillsunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Documentationunmatched
ERP (Enterprise Resource Planning)unmatched
FDA (Food and Drug Administration)unmatched
FDA Requirementsunmatched
Hospitalunmatched
Internal Auditunmatched
Laboratory Information Management System (LIMS)unmatched
Maintain Complianceunmatched
Manufacturingunmatched
Manufacturing Operationsunmatched
Operations Managementunmatched
Outsourcingunmatched
People Managementunmatched
Pharmacyunmatched
Process Improvementunmatched
Quality Assuranceunmatched
Records Managementunmatched
Regulationsunmatched
Standard Operating Procedures (SOP)unmatched
State Laws and Regulationsunmatched
Team Playerunmatched
United States Drug Enforcement Agency (DEA)unmatched
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