Job Details

  • Title: Associate Scientist
  • Code: RCI-7947
  • Location: Thousand Oaks, California 91320 (Temporary Remote)
  • Posted Date: 11/20/2020
  • Duration: 12 Months
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  Job Description

The Scientist role in Commercial Process Development will be part of a team responsible for authoring method transfer and method validation protocols and reports for late stage programs for the following method platforms: Chromatography, Bioassay, Device, PCR, Microbiology, Immunoassay, CE/Gel, Viral, and General. Protocols and reports will be authored according to regulatory and industry guidelines (i.e., ICH). This individual will support clinical and commercial locations throughout the company.

Basic Qualifications: Pharma or Biotech

  • Master’s degree and 3 years of Operations or Scientific experience OR Bachelor’s degree and 3 years of Operations or Scientific experience OR Associate’s degree and 10 years of Operations or Scientific experience OR High school diploma / GED and 12 years of Operations or Scientific experience
  • Scientific writing skills, reviewing and writing technical documentation for analytical methods
  • Master in Biochemistry, Analytical Chemistry, Physical or Life Sciences
  • Strong understanding of method validation/transfer for methods within the following platforms Chromatography, Bioassay, PCR, Microbiology, Immunoassay, CE, Gel, Device, Viral, and General (compendia)
  • Direct experience with method transfer and method validation processes from a Pharmaceutical or Biotechnology Company
  • Knowledge of analytical methods/technologies used in biologic and synthetic development and manufacturing
  • Excellent written and oral communication skills for the timely documentation, presentation, and discussion of scientific results in a fast-paced, multi-disciplinary, team-based environment
  • Demonstrated ability to critically analyze and interrogate various analytical data sets to drive and influence the process
  • Demonstrated ability to propose and drive new scientific initiatives