Pharmaceutical Blender Operator I — cGMP Production

Aveva Drug Delivery Systems

Florida

On-site

USD 28,000 - 30,000

Full time

14 days+

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Job summary

Aveva Drug Delivery Systems in Miramar, FL seeks a Blender Operator I to perform pharmaceutical blending and compounding following batch records and SOPs. You will handle APIs, potent compounds, solvents, and hazardous materials in a cGMP environment.

Responsibilities include equipment setup, material dispensing, in-process checks, GMP documentation, and maintaining clean, inspection-ready areas with strict safety practices.

Qualifications

  • Requires high school diploma or GED; technical certification preferred.
  • Minimum 5 years in pharma/regulated manufacturing.
  • Experience with potent compounds or hazardous materials preferred.
  • Ability to read and execute batch records and SOPs in English.

Responsibilities

  • Perform blending and compounding per approved batch records and SOPs.
  • Handle APIs, potent compounds, adhesives, solvents, and other hazardous materials.
  • Assemble, operate, clean, and sanitize blending equipment and related systems.
  • Perform raw material dispensing, weighing, staging, and verification.
  • Conduct batch record calculations, material reconciliation, and yield checks.
  • Complete in-process checks, sampling, and coat weight verifications as required.
  • Monitor process parameters (temperature, speeds, vacuum, pressure, times).
  • Maintain GMP documentation and ensure inspection readiness and data integrity.
  • Work with cross-functional teams to support production schedules and safety.

Skills

cGMP knowledge
GDP practices
Batch records
English reading/writing
Math proficiency
Team collaboration

Education

High school diploma/GED

Job description

Aveva Drug Delivery Systems in Miramar, FL seeks a Blender Operator I to perform pharmaceutical blending and compounding following batch records and SOPs. You will handle APIs, potent compounds, solvents, and hazardous materials in a cGMP environment.

Responsibilities include equipment setup, material dispensing, in-process checks, GMP documentation, and maintaining clean, inspection-ready areas with strict safety practices.

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