Senior Scientist I, Biologics Process Development

AbbVie

Worcester (MA)

On-site

USD 110,000 - 150,000

Full time

2 days ago
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Job summary

AbbVie Bioresearch Center in Worcester, MA is seeking a Senior Scientist I to join the Manufacturing Science and Technology (MSAT) team. You will lead process development activities for large-scale GMP cell culture processes, drive technology transfer, and support regulatory filings.

The role emphasizes mentorship, cross-functional collaboration with analytics, manufacturing, quality, and regulatory teams, and applying data analysis or programming skills to improve product quality and process

Qualifications

  • Bachelor’s degree or higher with significant experience in bioprocess development.
  • Thorough theoretical and practical understanding of own scientific discipline.

Responsibilities

  • Lead design, execution, and data-analysis for process development, characterization, validation, and continuous process verification for large-scale GMP cell culture processes.
  • Identify and develop technologies to improve product quality and process efficiency for biologics manufacturing.
  • Lead technology and process transfer activities to GMP scale across AbbVie’s manufacturing network.
  • Solve technical issues and support GMP manufacturing of therapeutic proteins.
  • Participate in cross-functional teams to support CMC sections of regulatory filings.
  • Author technical reports and validation documents.
  • Interact with cross-functional groups and external collaborators.
  • Preserve autonomy and productivity in laboratory research.

Skills

Process development
Data analysis
Programming
Team leadership

Education

Bachelor’s degree or equivalent
Master’s degree or equivalent
PhD

Tools

GMP

Job description

AbbVie Bioresearch Center in Worcester, MA is seeking a Senior Scientist I to join the Manufacturing Science and Technology (MSAT) team. You will lead process development activities for large-scale GMP cell culture processes, drive technology transfer, and support regulatory filings.

The role emphasizes mentorship, cross-functional collaboration with analytics, manufacturing, quality, and regulatory teams, and applying data analysis or programming skills to improve product quality and process

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