Pharmacist

RXinsider LTD.; Phoenix (AZ); On-site; USD 120,000 - 150,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Job summary

RXinsider LTD. is seeking a full-time Pharmacist in Phoenix, AZ to support sterile injectable manufacturing operations in a highly regulated environment.

The role involves ensuring compounding, labeling, and documentation align with FDA, USP standards, and internal SOPs, while supervising compounding and batch record verification. The position requires a current Arizona Pharmacist license and 2–3 years of sterile compounding experience, with opportunities for long-term growth within a 503B or

Qualifications

• Arizona Pharmacist license in good standing
• 2–3 years of sterile compounding experience
• Knowledge of USP, cGMP, and FDA manufacturing guidelines

Responsibilities

• Review and approve batch production records, labels, and related documentation
• Supervise sterile compounding and aseptic filling operations for compliance
• Verify and document calculations for compounding and formulation accuracy
• Monitor cleanroom operations, gowning, 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 QA and Production to maintain ongoing compliance
• Provide guidance to technicians on cGMP and pharmacy standards
• Participate in deviations reviews, investigations, and process improvements

Skills

Sterile compounding

FDA guidelines

USP standards

Documentation

Communication

Teamwork

Education

Arizona Pharmacist License

Tools

LIMS

ERP

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