Demo

Analytical Scientist

Diati Staffing
Germantown, MD Full Time
POSTED ON 1/17/2025
AVAILABLE BEFORE 4/2/2025

The qualified individual should have experience in sample testing and product characterization using electrophoretic technologies such as SDS-PAGE, pH, total protein analysis including A280 and Western Blot. Experience or knowledge on other analytical technology such as PCR based assays is a plus.

Responsibilities include but not limited to :

  • Follow SOP to test in-process samples using SDS-PAGE densitometry, Western Blot, pH, and Total Protein via A280 to support process development and stability studies of nanoparticle vaccines.
  • Analyze gel image data using Image Lab and document in-process testing data.
  • Optimize and troubleshoot SDS-PAGE and Western Blot assays.
  • Participate in qualification of in-process assays.
  • Present sample testing data at internal meetings.
  • Thoroughly analyze results and methods, solve analytical problems, troubleshoot assays and meet experimental expectations for analytics.
  • Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
  • Maintain effective communication within Analytical Development and cross-functional teams.
  • Present scientific findings at internal and external meetings (if applicable).

Minimal Requirements :

  • MS in analytical science, chemistry, biochemistry, or related field with 4 years of industry experience in biopharmaceutical and / or vaccine development.
  • BS in analytical science, chemistry, biochemistry, or related field with 6 years of industry experience in biopharmaceutical and / or vaccine development.
  • Ability to critically analyze data using statistical tools and to compile and review technical reports.
  • Ability to define priorities and process to get things done.
  • Knowledge and expertise in principles and practice of current Good Manufacturing Practices (GMPs) is preferred.
  • Excellent record keeping abilities to adequately record, analyze, and document analytical data generated in support of regulatory requirements.
  • Good understanding of statistical tools and knowledge of DOE (Design of Experiments) and QbD (Quality by Design) principles is a plus.
  • Strong communication, presentation, and writing skills.
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