Validation Engineer

Job Summary

Seeking a Validation Engineer with 4-7 years of experience, the full-time position will support validation activities across GMP-regulated environments by developing, executing, and maintaining validation lifecycle documentation while ensuring compliance with regulatory requirements.

Key Responsibilities:

• Generate and execute validation lifecycle documentation, including FAT, SAT, IQ, OQ, PQ, and validation reports
• Provide validation support for MES and eBR implementation, qualification, and lifecycle management activities
• Review validation documentation and ensure compliance with approved methodologies and regulatory requirements

Required Qualifications:

• Bachelor's degree in Engineering, Life Sciences, Computer Systems, or a related technical field
• 4-7 years of validation experience in the pharmaceutical, biotechnology, or regulated life sciences industry
• Experience with equipment qualification and computerized systems validation activities
• Familiarity with risk-based validation methodologies and GMP environments
• Experience supporting audits, inspections, and deviation investigations is preferred