Validation Engineer

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