Sterile Compounding Tech II — 503B Manufacturing

Aveva Drug Delivery Systems

Fort Lauderdale (FL)

Presencial

USD 33.000 - 44.000

Jornada completa

hace 12 horas
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Descripción de la vacante

Aveva Drug Delivery Systems is seeking a Sterile Compounding Pharmacy Technician II to join our 503B outsourcing facility in Fort Lauderdale. You will independently perform sterile and hazardous drug batch compounding per approved batch records.

The role supports environmental monitoring and deviation investigations, maintains GDP compliance, and assists in training Technician I staff while upholding aseptic technique during FDA audits.

Formación

  • High school diploma or equivalent.
  • Active Pharmacy Technician registration.
  • 2–4 years sterile compounding experience.
  • Competency in cGMP, USP standards.
  • Media fill and fingertip qualification current cycle.

Responsabilidades

  • Independently compound sterile and hazardous drug batch per batch records.
  • Verify materials, calculations, and batch setup prior to compounding.
  • Maintain GDP compliance and inspection readiness for batch records.
  • Support environmental monitoring, investigations, and corrective actions.
  • Assist in onboarding and hands-on training of Technician I staff.
  • Maintain aseptic technique during FDA audits and inspections.
  • Support equipment cleaning, sanitization, and room readiness.
  • Identify and elevate deviations, EM excursions, or process risks.

Conocimientos

Sterile compounding
HD handling
Aseptic technique
Documentation

Educación

High school diploma or equivalent

Descripción del empleo

Aveva Drug Delivery Systems is seeking a Sterile Compounding Pharmacy Technician II to join our 503B outsourcing facility in Fort Lauderdale. You will independently perform sterile and hazardous drug batch compounding per approved batch records.

The role supports environmental monitoring and deviation investigations, maintains GDP compliance, and assists in training Technician I staff while upholding aseptic technique during FDA audits.

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