Principal Biologics Process Analytics Scientist

University of Georgia- FACS

Worcester (MA)

Hybrid

USD 120,000 - 160,000

Full time

2 days ago
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Job summary

AbbVie is seeking a Principal Research Scientist I to join the Late-Stage Process Analytics group within the Analytical Development team in the Biologics division. The role focuses on supporting analytical aspects of biologics programs, leading methods like HPLC and capillary electrophoresis, and collaborating across cross-functional teams.

Ideal candidates have a PhD with 6+ years of biotech/pharma experience, strong technical writing skills for regulatory submissions, and proven leadership to

Qualifications

  • PhD in chemistry, biology, biochemistry, chemical engineering, or related technical discipline.
  • Minimum of 6+ years (PhD) of relevant professional experience in biotech/pharmaceutical setting.

Responsibilities

  • Act as process analytics lead for late-stage biologics in AbbVie's CMC teams and collaborate with development groups.
  • Serve as subject matter expert for separation-based methods like HPLC and capillary electrophoresis for Mab/DS programs.
  • Evaluate and select analytical technologies to meet program needs and ensure timely delivery of results.
  • Provide hands-on lab support and assist in method development, execution, and troubleshooting.
  • Write and review technical documents for late-stage programs and support IND/BLA filings.
  • Mentor and supervise junior scientists and foster an inclusive team environment.

Skills

Leadership
Communication
Cross-functional collaboration
Mentoring
Analytical thinking

Education

PhD in chemistry/biochemistry/biological engineering

Tools

HPLC
Capillary electrophoresis

Job description

AbbVie is seeking a Principal Research Scientist I to join the Late-Stage Process Analytics group within the Analytical Development team in the Biologics division. The role focuses on supporting analytical aspects of biologics programs, leading methods like HPLC and capillary electrophoresis, and collaborating across cross-functional teams.

Ideal candidates have a PhD with 6+ years of biotech/pharma experience, strong technical writing skills for regulatory submissions, and proven leadership to

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