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Sterile Compounding Pharmacy Technician II

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Onsite

Sterile Compounding Pharmacy Technician II

DifGen Pharmaceuticals

Sterile Compounding Pharmacy Technician II

Skills

Internal AuditCompliance

13 days ago

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Important information


Contract type:

Permanent

Salary:

$54,080 – $64,480 / year

Location:

Tamarac, FL, USA

Work mode:

Onsite

Published on:

14 October 2026

What they need


Description

About Us:

Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies. We are dedicated to advancing solutions that optimize the efficacy, safety, and precision of pharmaceutical treatments. Join our team and help shape the future of healthcare by contributing to the development of groundbreaking drug delivery systems that improve patient outcomes worldwide.

Position Summary

The Sterile Compounding Pharmacy Technician II independently performs sterile and hazardous drug batch compounding within a 503B outsourcing facility. This role executes complex aseptic operations, ensures batch documentation accuracy, and supports environmental monitoring and deviation investigations under the direction of the Compounding Pharmacist

Key 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 escalate 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

Qualifications

Minimum Qualifications

  • High school diploma or equivalent
  • Active Pharmacy Technician registration
  • Minimum 2 - 4 years sterile compounding experience
  • Demonstrated competency in cGMP, USP <797> and <800> requirements
  • Media fill and fingertip qualification in current cycle

Preferred Qualifications

  • CSPT certification
  • cGMP experience
  • Experience in FDA-registered 503B operations
  • Familiarity with batch manufacturing scale operations

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