Sterile Compounding Tech II — 503B GMP Expert

Aveva Drug Delivery Systems; Florida; On-site; USD 29,000 - 35,000; Full time

Job summary

Aveva Drug Delivery Systems, a pharmaceutical manufacturer, is seeking a Sterile Compounding Pharmacy Technician II in Tamarac, FL. The role performs complex aseptic operations in a 503B outsourcing facility and ensures batch documentation accuracy under the direction of the Compounding Pharmacist.

The incumbent will handle sterile and hazardous drug batches, support environmental monitoring, and participate in investigations and audits, while maintaining GDP compliance and room readiness.

Qualifications

• Minimum 2–4 years sterile compounding experience.
• Demonstrated competency in cGMP, USP <797> and <800> requirements.
• Media fill and fingertip qualification in current cycle.

Responsibilities

• Independently compound sterile and hazardous drug batches per approved batch records.
• Handle HD APIs and finished formulations in compliance with USP <800>.
• Verify materials, calculations, and batch setup prior to compounding.
• Complete batch records with full GDP compliance and inspection readiness.
• Participate in and support environmental monitoring, investigations, and corrective actions.
• Identify and elevate deviations, EM excursions, or process risks.
• Support onboarding and hands-on training of Technician I staff.
• Maintain aseptic technique and compliance during FDA and internal audits.
• Support equipment cleaning, sanitization, and room readiness.

Skills

Sterile compounding

FDA compliance

Documentation accuracy

Batch records

cGMP knowledge

Media fill

Education

High school diploma or equivalent

Job description

Aveva Drug Delivery Systems, a pharmaceutical manufacturer, is seeking a Sterile Compounding Pharmacy Technician II in Tamarac, FL. The role performs complex aseptic operations in a 503B outsourcing facility and ensures batch documentation accuracy under the direction of the Compounding Pharmacist.

The incumbent will handle sterile and hazardous drug batches, support environmental monitoring, and participate in investigations and audits, while maintaining GDP compliance and room readiness.