Job Title: Equipment Validation Engineer Summary: Responsible for the planning, execution, and documentation of equipment qualification and validation activities within a GMP-regulated pharmaceutical manufacturing environment. Ensures that all equipment meets regulatory requirements and company quality standards. Responsibilities: Develop and execute validation protocols (IQ, OQ, PQ). Generate and maintain accurate validation documentation. Perform risk assessments related to equipment validation. Coordinate with cross-functional teams (QA, manufacturing, engineering). Ensure compliance with GMP and relevant regulatory guidelines. Troubleshoot and resolve validation deviations. Manage equipment calibration and maintenance related to validation. Review and approve validation related documentation. Qualifications: Bachelor's degree in Engineering or a related science field. Experience in equipment qualification and validation in a GMP environment. Strong understanding of GMP regulations and industry standards. Excellent documentation and communication skills. To start the process click the Continue to Application or Login/Register to apply button below.