Validation Specialist - Analytical Instruments

Consulting San Diego, California


3-10 years validation experience. Must have analytical instruments qualification experience. CSV for analytical instruments preferred.

  • 3-10 years’ experience in validation services in a regulated, manufacturing environment within the biotechnology, pharmaceutical, or cell and gene therapy
  • Hands on experience in executing C&Q protocols for  QC lab equipment and processes.
  • Experience in Computer System Validation for lab instruments is desired
  • Strong knowledge of FDA, EU and cGMP regulations and good documentation practices
  • Ability to create all validation lifecycle documetns
  • Proficient in Microsoft Word, Excel, PowerPoint