Biologics Manufacturing Operator II — Entry-Level

AbbVie

Barceloneta (PR)

On-site

USD 43,000 - 58,000

Full time

6 days ago
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Benefits offered by this job

Paid time off
Medical/dental/vision insurance
401(k)
Short-term incentive programs

Job summary

AbbVie seeks operators for bulk biologics manufacturing, performing cleaning, sterilization, process tests, and equipment assembly in aseptic and non-aseptic environments. You will work across Media & Buffer Formulation, Upstream, and Downstream areas, documenting statuses and addressing deviations.

The role emphasizes cGMP adherence, SOP compliance, and collaboration with EHS programs to ensure safe, compliant production.

Qualifications

  • Associate degree in science, mechanics, electricity, instrumentation or related field.
  • No previous experience required.
  • Basic knowledge of laboratory techniques.
  • Basic knowledge of computerized systems such as DeltaV, MES and SAP preferred.
  • Basic mechanical and mathematical skills.
  • Basic verbal and written communication skills in English and Spanish.

Responsibilities

  • Operate manufacturing equipment and instruments such as tanks, autoclaves, filtration systems, washers and pH controls.
  • Manufacture of bulk biologics in Media & Buffer Formulation, Inoculum or Fermentation, and Capture/Purification areas.
  • Conduct equipment and facility inspections and elevate any deviations.
  • Provide technical assistance to manufacturing areas for troubleshooting.
  • Receive, inspect and verify materials for production activities.
  • Document batch records and process/equipment status.
  • Sample collection and processing as required.
  • Adhere to cGMP, SOPs and related documentation.
  • Support environmental health and safety procedures and continuous improvement.

Skills

Laboratory techniques
Mechanical skills
Mathematical skills
Bilingual English/Spanish

Education

Associate Degree in Science/Mech/Elec/Instrumentation

Tools

DeltaV
MES
SAP

Job description

AbbVie seeks operators for bulk biologics manufacturing, performing cleaning, sterilization, process tests, and equipment assembly in aseptic and non-aseptic environments. You will work across Media & Buffer Formulation, Upstream, and Downstream areas, documenting statuses and addressing deviations.

The role emphasizes cGMP adherence, SOP compliance, and collaboration with EHS programs to ensure safe, compliant production.

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