Validation Analyst: GMP Method Validation & Lab Data

SysTech US; United States; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Referral bonus

Job summary

Systechcorp, Inc. is seeking Validation Analysts to join a GMP-regulated laboratory environment in New Jersey, with travel across the United States. The role focuses on analytical method development, validation/qualification, and regulatory compliance.

Responsibilities include data recording and analysis using Microsoft Excel, performing aseptic techniques, preparing media, stocks, and reagents, and contributing to audits and performance qualification activities.

Qualifications

• Involve analytical method development, validation/qualification, GMP operations, and regulatory compliance.
• Record and analyze process data using Microsoft Excel.
• Prepare sterile media and reagents; apply aseptic techniques for sample handling.

Responsibilities

• Design validation study features and conduct audits/qualification to ensure regulatory compliance.
• Perform essential lab functions including preparation of sterile growth media, stock solutions, and reagents.

Education

Master’s degree in Science, Technology, or Engineering (any)

Job description

Systechcorp, Inc. is seeking Validation Analysts to join a GMP-regulated laboratory environment in New Jersey, with travel across the United States. The role focuses on analytical method development, validation/qualification, and regulatory compliance.

Responsibilities include data recording and analysis using Microsoft Excel, performing aseptic techniques, preparing media, stocks, and reagents, and contributing to audits and performance qualification activities.