Pharmacist

Medivant Healthcare; Phoenix (AZ); On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

Paid time off and holidays

Career growth opportunities

Job summary

Medivant Healthcare in Phoenix, AZ seeks a Full-Time Pharmacist to support sterile injectable manufacturing. You will ensure compounding, labeling, and documentation meet FDA, USP, and internal SOPs, verify batch records, and supervise operations while maintaining QA compliance.

Responsibilities include supervising sterile filling, documenting calculations, and supporting audits and deviations investigations to drive continuous improvement in a highly regulated cGMP environment.

Qualifications

• Active Pharmacist License in Arizona in good standing.
• 2–3 years of sterile compounding or 503B facility experience.
• Strong understanding of USP, cGMP, and FDA guidelines.
• Strong documentation, verification, and analytical skills.

Responsibilities

• Review and approve batch production records, labels, and documentation.
• Supervise sterile compounding and aseptic filling for compliance.
• Verify calculations for compounding formulations.
• Monitor cleanroom operations, gowning, and aseptic techniques.
• Support audits, CAPA investigations, and validations.
• Ensure compliance with DEA, FDA, and state pharmacy regulations.
• Collaborate with QA and Production to maintain compliance.
• Provide guidance to technicians on cGMP standards.
• Review deviations, investigations, and process improvements.

Skills

Active AZ Pharmacist License

Sterile compounding experience

Documentation & QA

Communication & teamwork

Tools

LIMS familiarity

ERP familiarity

Electronic batch records

Job description

Position Summary

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 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 / 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 , USP , 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