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Validation Document Coordinator

2 months ago

Foster City, United States Unicon Pharma Inc Full time

Join our team as a Document Coordinator. If you have a strong background in biotechnology, process validation, or quality assurance, we want to hear from you


Key Responsibilities:

  • Develop and implement procedures and best practices for Biologics Process Validation.
  • Act as a Project Manager, tracking and monitoring Process Validation deliverables.
  • Coordinate and manage Process Validation documentation, ensuring alignment across teams.
  • Perform Data Verification on completed studies and reports.

What We're Looking For:

  • Bachelor's degree in life sciences or a related field.
  • Minimum of four years of experience in biotechnology, process validation, or a related area.
  • Strong understanding of GMP principles and process validation in regulated environments.