Part-Time Sterile Compounding Pharmacist & QA Oversight

Tailstorm-Health-Inc; Chandler (AZ); On-site; USD 68,000 - 83,000; Part time

Job summary

Medivant Healthcare in Chandler, AZ seeks a licensed Pharmacist to support sterile injectable manufacturing, ensuring FDA, USP, and cGMP compliance and robust quality documentation.

You will collaborate with Production, QA, and Regulatory teams; require at least 2 years in sterile compounding or related pharmaceutical manufacturing; strong attention to detail and documentation skills are essential.

Qualifications

• Arizona active Pharmacist license in good standing.
• Minimum 2 years in sterile compounding, pharmaceutical manufacturing, hospital pharmacy, or a 503B outsourcing facility.
• Strong knowledge of USP 797, USP 800, cGMP and FDA regulations.
• Experience reviewing manufacturing documentation and batch production records.
• Strong analytical, problem-solving, and communication skills.
• Ability to work in a regulated pharmaceutical manufacturing environment.

Responsibilities

• Oversee sterile compounding and aseptic filling to ensure USP 797/800 and cGMP compliance.
• Monitor cleanroom operations, gowning practices, environmental controls, and aseptic techniques.
• Verify formulation calculations and compounding accuracy.
• Ensure adherence to SOPs and manufacturing procedures.
• Provide guidance to technicians on sterile compounding practices.
• Review batch production records and labels for accuracy.
• Support audits, inspections, and quality systems.

Skills

Sterile compounding

Regulatory compliance

FDA regulations

Batch records

Quality documentation

Cross-functional collaboration

Attention to detail

Gowning & cleanroom

Education

Arizona Pharmacist License

Tools

LIMS

ERP

Electronic batch records

Job description

Medivant Healthcare in Chandler, AZ seeks a licensed Pharmacist to support sterile injectable manufacturing, ensuring FDA, USP, and cGMP compliance and robust quality documentation.

You will collaborate with Production, QA, and Regulatory teams; require at least 2 years in sterile compounding or related pharmaceutical manufacturing; strong attention to detail and documentation skills are essential.