Senior Scientist, Peptide Analytics & DP Formulation

AbbVie

North Chicago (IL)

On-site

USD 120,000 - 180,000

Full time

14 days+

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Benefits offered by this job

Comprehensive benefits
Eligibility for incentive programs

Job summary

AbbVie in North Chicago, IL seeks a Senior Scientist I – Peptide Analytical Chemistry to conceive, develop, and execute analytical methods for peptide drug substance and drug product across preclinical and clinical spaces.

You will collaborate across the global Analytical R&D organization and with cross-functional partners to advance DP/DS projects, perform method development and validation, and contribute to regulatory documentation.

Qualifications

  • Minimum degrees as listed; PhD preferred for senior analytical focus.
  • Strong background in peptides and small-molecule analytics.
  • Ability to independently develop and troubleshoot complex methods.

Responsibilities

  • Lead peptide DP formulation development with analytical support.
  • Provide analytical expertise for diverse peptide formulations.
  • Develop and implement drug product analytical strategies.
  • Support substance characterization to inform formulations.
  • Develop, validate, and transfer analytical methods and data packages.
  • Utilize analytical techniques to profile impurities and products.

Skills

Analytical chemistry
Analytical problem-solving
Cross-functional collaboration
Written & oral communication
Mentoring junior scientists
Learning mindset

Education

Bachelor's degree in Analytical Chemistry or Pharmaceutical Sciences
Master's degree in Analytical Chemistry or Pharmaceutical Sciences
PhD in Analytical Chemistry or Pharmaceutical Sciences

Tools

HPLC/UHPLC
HRMS
LC-MS/MS
Chiral separation

Job description

AbbVie in North Chicago, IL seeks a Senior Scientist I – Peptide Analytical Chemistry to conceive, develop, and execute analytical methods for peptide drug substance and drug product across preclinical and clinical spaces.

You will collaborate across the global Analytical R&D organization and with cross-functional partners to advance DP/DS projects, perform method development and validation, and contribute to regulatory documentation.

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