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Validation Analysts

SystechCorp. Full-Time Positions
South Plainfield, NJ; various locations throughout the United States Posted Jul 14, 2026
On-site

About this role

About the Role Validation Analysts perform analytical method development, method validation/qualification, and GMP laboratory operations to ensure compliance with quality standards and regulatory requirements. The role involves designing validation studies, conducting audits or qualification activities, and data analysis using Excel, with hands-on work in aseptic techniques and preparation of lab materials. What You'll Do

  • Involve in analytical method development, method validation/qualification, GMP laboratory operations, adherence to quality standards and regulatory analysis.
  • Design validation study features, such as sampling, testing, or analytical methodologies.
  • Conduct audits or performance qualification processes to ensure compliance with internal or regulatory requirements.
  • Record and analyze process and experimental data using Microsoft Excel.
  • Utilize advanced aseptic techniques for the management of shake flasks and prepare samples for analysis using sophisticated analytical instruments.
  • Perform essential lab functions including the preparation of sterile growth media, stock solutions, and reagents. What We're Looking For
  • Master’s degree in Science, Technology, or Engineering (any) is required.
  • Willingness to work at multiple locations; work location includes South Plainfield, NJ and various unanticipated locations throughout the U.S.
  • Experience with GMP, validation/qualification processes, and regulatory compliance is preferred based on responsibilities. Compensation & Benefits
  • Referral reward: $1,000 for successful referral.

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