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Sterile Compounding Pharmacy Technician II

AVEVA DRUG DELIVERY SYSTEMS INC
Posted 5 months ago, valid for 13 days
Location

Tamarac, FL, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Aveva Drug Delivery Systems is seeking a Sterile Compounding Pharmacy Technician II for a full-time position in Tamarac, FL.
  • The role requires a minimum of 2 to 4 years of sterile compounding experience and an active Pharmacy Technician registration.
  • Responsibilities include independently compounding sterile and hazardous drug batches, ensuring documentation accuracy, and participating in environmental monitoring.
  • Candidates should demonstrate competency in cGMP and USP <797> and <800> requirements, with media fill and fingertip qualification in their current cycle.
  • The salary for this position is not specified, but candidates with CSPT certification and experience in FDA-registered 503B operations are preferred.

Job DetailsJob Location: Tamarac, FL 33321Position Type: Full TimeJob Shift: DayAbout 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       QualificationsMinimum 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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