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Senior Research Associate II

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Tucker Parker Smith Group

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Location:
United States , Novato

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Category:
Research and Development

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Contract Type:
Not provided

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Salary:

45.00 USD / Hour
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Job Description:

This laboratory-based role focuses on analytical method development and characterization of biologics, working closely with cross-functional partners across research and process development teams.

Job Responsibility:

  • Perform analytical method development, qualification, and characterization for biologics including proteins, peptides, and protein-conjugates
  • Conduct biophysical and biochemical assays using techniques such as HPLC and Capillary Electrophoresis (CE)
  • Provide analytical testing and characterization support to Upstream/Downstream Process Development, Formulation, and Research teams
  • Document experimental work in electronic lab notebooks and contribute to technical documentation including test methods, reports, and procedures
  • Troubleshoot analytical challenges and contribute to continuous method improvement
  • Support laboratory operations including equipment maintenance, safety inspections, and lab organization
  • Present experimental data and findings in team meetings and technical discussions

Requirements:

  • Hands-on experience in biotechnology, pharmaceutical, or academic laboratories supporting analytical testing of biologics
  • Experience with biochemical characterization techniques, including: SEC, SCX, and RP-HPLC (Agilent, Waters, or Thermo systems)
  • Capillary Electrophoresis (PA800 or BioPhase 8800) including CE-SDS and glycan analysis
  • Strong understanding of analytical method development and troubleshooting
  • Excellent documentation, analytical, and communication skills
  • Ability to work independently and collaboratively in a fast-paced, cross-functional environment
  • Bachelor’s degree in Chemistry, Biochemistry, Analytical Chemistry, Chemical Engineering, or related field with 6 years of relevant experience OR Master’s degree with 4 years of relevant experience

Nice to have:

  • Experience with cIEF (Maurice) instrumentation
  • LC-MS method development experience (Orbitrap, QToF, or QQQ)
  • Experience with method qualification, transfer, and root cause investigations
  • Exposure to biopharmaceutical process development or laboratory automation

Additional Information:

Job Posted:
March 19, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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