Associate Scientist II, Solid Dosage Process Development

AbbVie

North Chicago (IL)

On-site

USD 85,000 - 120,000

Full time

3 days ago
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Job summary

AbbVie seeks a process development engineer to independently generate data supporting development, characterization, and scale-up of oral solid dosage forms. You will analyze results, support manufacturing campaigns, and contribute to regulatory documentation, while ensuring GMP/GxP compliance and data integrity.

Responsibilities include executing DOE studies, interpreting results, and providing on-site technical support for campaigns and PPQ batches, with emphasis on safety and quality in a

Qualifications

  • BS with 3+ years or MS in Engineering/Pharma related field.
  • Experience supporting development or manufacturing of oral solid dosage forms.
  • Familiarity with DOE and statistical data analysis.

Responsibilities

  • Perform routine lab and pilot-scale activities, generating reliable results.
  • Analyze results, identify trends, deviations.
  • Troubleshoot experiments and process challenges.
  • Learn and apply new scientific/engineering techniques.
  • Execute process development, characterization and scale-up studies for oral solids.
  • Demonstrate skill in multiple techniques and modify protocols as needed.
  • Execute designed experiments (DOE) and apply statistical tools.
  • Support manufacturing campaigns, scale-up, and PPQ batches on-site.
  • Prepare campaign memos, technical summaries, and development docs.
  • Adhere to safety, data integrity, GMP/GxP standards and material handling.

Skills

DOE experience
Statistical analysis
Data interpretation
Problem solving

Education

Bachelor's or Master's in Engineering or Pharmaceutical Sciences

Tools

Statistical software

Job description

AbbVie seeks a process development engineer to independently generate data supporting development, characterization, and scale-up of oral solid dosage forms. You will analyze results, support manufacturing campaigns, and contribute to regulatory documentation, while ensuring GMP/GxP compliance and data integrity.

Responsibilities include executing DOE studies, interpreting results, and providing on-site technical support for campaigns and PPQ batches, with emphasis on safety and quality in a

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