Pharmacist

About the Role

The Full-Time Pharmacist supports Medivant’s sterile injectable manufacturing operations by ensuring all compounding, labeling, and documentation processes comply with FDA regulations, USP, and internal SOPs. This role offers long-term career growth, stability, and the opportunity to work in a highly regulated cGMP manufacturing environment.

Responsibilities

• Review and approve batch production records, labels, and associated documentation
• Supervise sterile compounding and aseptic filling operations to ensure compliance with USP 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

Requirements

• 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, cGMP, and FDA manufacturing guidelines
• Strong documentation, verification, and analytical skills
• Excellent communication and teamwork abilities

Preferred Qualifications

• 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

Benefits

• 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

Pay

Competitive base salary (based on experience).