Associate Scientist, Analytical Development

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.