Senior Research Associate Job at GForce Life Sciences, Novato, CA

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  • GForce Life Sciences
  • Novato, CA

Job Description

Senior Research Associate

7-month Contract

Onsite in Novato, CA

Must be able to work on a W2

Requirements

  • Support the Separations and Biophysics group within the Analytical Sciences function.
  • Perform hands-on laboratory work supporting biophysical and biochemical assay development and qualification using HPLC and Capillary Electrophoresis (CE) for various modalities, preferably biologics.
  • Support analytical characterization and routine testing for partner groups including Upstream and Downstream Process Development, Formulation, and Research and Early Development teams.
  • Document experimental results in an electronic lab notebook system and contribute to technical documentation including procedures, test methods, and development reports.
  • Participate in operational laboratory activities including safety inspections, lab organization, supply ordering, and routine equipment maintenance.
  • Present scientific literature and experimental results during group meetings and internal discussion forums.
  • Perform other related duties as assigned.

Qualifications

  • Bachelor’s degree in Chemistry, Biochemistry, Analytical Chemistry, Chemical Engineering, or a related field with 6+ years of experience in a biologics or pharmaceutical environment, or
  • Master’s degree in Chemistry, Biochemistry, Analytical Chemistry, Chemical Engineering, or a related field with 4+ years of experience in a biologics or pharmaceutical environment.

Technical Experience

  • Hands-on experience with analytical testing and characterization techniques for proteins, peptides, and protein-conjugates in either a biotechnology industry or academic setting.
  • Experience with biochemical characterization methods including:
  • SEC, SCX, and RP-HPLC using Agilent, Waters, or Thermo LC instruments.
  • Capillary Electrophoresis methods such as SDS-based size separation and glycan profiling using systems such as PA800 or BioPhase8800.
  • Experience with cIEF systems such as Maurice is highly desirable.
  • LC-MS method development experience (Orbitrap, QToF, or QQQ) is desirable.
  • Understanding of analytical testing processes, regulatory considerations, method qualification, and method transfer.
  • Experience with statistical software, electronic document management systems, and laboratory information management systems.

Job Tags

Contract work

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