Senior Scientist - Formulation & Parenteral Development

AbbVie Inc.

Northern (KY)

Hybrid

USD 90,000 - 130,000

Full time

37 hours ago
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Job summary

AbbVie in Kentucky, United States is seeking a highly qualified scientist/engineer to own formulation development, process optimization, and technology transfers. You will plan and execute lab studies, perform parenteral drug product activities, and analyze data to support high-quality medicines.

Collaboration with engineering, quality, and manufacturing teams is essential. The role emphasizes GMP compliance, data integrity, and ongoing improvements in sterile manufacturing and parenteral

Qualifications

  • Bachelor's, Master's, or PhD in Pharmaceutical Science, Biotechnology, Chemical/Process Engineering, Drug Discovery & Development, or a related field.
  • Experience in pharmaceutical, biotechnology, medical device, or regulated lab environments.
  • Experience planning and executing scientific experiments independently.
  • Knowledge of GMP/GxP, quality systems, validation concepts, and data integrity.
  • Experience with sterile manufacturing or parenteral technologies is a plus.

Responsibilities

  • Design and execute laboratory studies to support formulation development and scale-up.
  • Perform parenteral drug product activities including compounding, filtration, and filling.
  • Analyze data, identify trends, troubleshoot, and make data-driven recommendations.
  • Author and review technical documents, protocols, reports, and batch records.
  • Support lab start-up activities, equipment qualification, and facility readiness.
  • Collaborate with engineering, quality, and manufacturing teams to evaluate equipment and systems.
  • Lead or contribute to investigations, risk assessments, change controls, and problem-solving.
  • Ensure GMP, quality, data integrity, and safety requirements.
  • Drive continuous improvement, digitalization, and knowledge-sharing.

Skills

Analytical skills
Problem-solving
Cross-functional collaboration
Data interpretation
Regulatory compliance
Documentation

Education

Pharmaceutical Science
Biotechnology
Chemical or Process Engineering
Drug Discovery & Development
Other relevant scientific or engineering discipline

Job description

AbbVie in Kentucky, United States is seeking a highly qualified scientist/engineer to own formulation development, process optimization, and technology transfers. You will plan and execute lab studies, perform parenteral drug product activities, and analyze data to support high-quality medicines.

Collaboration with engineering, quality, and manufacturing teams is essential. The role emphasizes GMP compliance, data integrity, and ongoing improvements in sterile manufacturing and parenteral

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