Aseptic Parenteral Manufacturing Operator I

AbbVie Inc.

Barceloneta (PR)

Sur place

USD 19 000 - 36 000

Plein temps

Il y a 3 jours
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Avantages offerts par ce poste

Paid time off
Medical/dental/vision insurance
401(k)

Résumé du poste

AbbVie Inc. is seeking a manufacturing operator in Barceloneta, Puerto Rico to operate equipment in filling or compounding, inspect and pack syringes, and ensure sterile and non-sterile processes meet quality standards.

The role requires adherence to cGMP and extensive documentation in electronic or paper batch records. Responsibilities include cleaning and sterilizing equipment, verifying material readiness, monitoring critical process parameters, and supporting EHS programs.

Qualifications

  • Associate degree or equivalent in science, mechanics, electricity, instrumentation, or related field.
  • Basic knowledge of laboratory techniques.
  • Familiarity with DeltaV, MES and SAP preferred.
  • Good verbal and written English and Spanish communication.

Responsabilités

  • Inspect and pack syringes of biologic parenteral product.
  • Clean, prepare and sterilize manufacturing equipment for parenteral use.
  • Conduct equipment and facility inspections and report deviations.
  • Receive, inspect and verify materials for production.
  • Document batch records in electronic or paper systems.
  • Monitor critical parameters and address deviations per SOPs.
  • Adhere to cGMP and EHS procedures and maintain records.
  • Support environmental health and safety initiatives.

Connaissances

Laboratory techniques
Math skills
English/Spanish communication
Basic mechanical skills

Formation

Associate Degree in Science, Mechanics, Electricity, or Instrumentation

Outils

DeltaV
MES
SAP

Description du poste

AbbVie Inc. is seeking a manufacturing operator in Barceloneta, Puerto Rico to operate equipment in filling or compounding, inspect and pack syringes, and ensure sterile and non-sterile processes meet quality standards.

The role requires adherence to cGMP and extensive documentation in electronic or paper batch records. Responsibilities include cleaning and sterilizing equipment, verifying material readiness, monitoring critical process parameters, and supporting EHS programs.

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