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Scientist III

Job in Fort Sheridan, Lake County, Illinois, 60037, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-03-04
Job specializations:
  • Engineering
    Research Scientist, Biotechnology
  • Science
    Research Scientist, Biotechnology
Job Description & How to Apply Below
Location: Fort Sheridan

Job Description:

  • Product Development Science and Technology (PDS&T) is seeking a motivated Scientist to support parenteral drug product process development, scale-up, and technology transfer to commercial manufacturing sites. This role will focus on the development of robust manufacturing processes for clinical and commercial-phase products, with an emphasis on antibody-drug conjugates (ADCs).
  • The Scientist will independently design and execute laboratory studies, generate and analyse precise and reproducible data, and contribute to cross-functional product development and Chemistry, Manufacturing, and Controls (CMC) teams.
Responsibilities:
  • Design and execute studies to develop and optimize manufacturing processes for parenteral drug products.
  • Conduct stability assessments of biologics by evaluating their chemical and physical properties under various conditions, including pH, ionic strength, temperature, light, and moisture exposure.
  • Assess the impact of manufacturing process stresses (e.g., freeze-thaw cycles, mixing, filtration, filling, and lyophilization) on product stability and performance.
  • Interpret experimental results, identify significant deviations, and propose and execute follow-up studies to refine process parameters.
  • Support scale-up activities and technology transfer to commercial manufacturing sites.
  • Prepare technical reports, regulatory documentation, and presentations to communicate findings effectively.
Requirements:
  • Bachelor's degree in chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field with 7+ years of relevant experience, OR.
  • Master's degree with 3+ years of experience, OR.
  • PhD with 0+ years of experience.
  • Strong background in parenteral drug product development, particularly ADCs.
  • Experience with formulation stability studies and analytical techniques for biologics.
  • Demonstrated ability to analyse data, troubleshoot experiments, and optimize processes.
  • Excellent scientific writing and verbal communication skills.
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