Role Overview: A CQV Engineer is responsible for ensuring that equipment, systems, and processes in pharmaceutical and biotechnology facilities meet regulatory and operational requirements. They play a key role in commissioning, qualification, and validation activities to ensure compliance with GMP (Good Manufacturing Practices) and other industry standards. Job Location: Ireland, Denmark&Germany Key Responsibilities: * Execute commissioning, qualification, and validation (CQV) protocols for equipment, utilities, and processes. * Develop and review validation protocols (IQ, OQ, PQ). * Perform risk assessments and gap analysis to ensure compliance with regulatory requirements. * Work closely with engineering, quality, and operations teams to troubleshoot and resolve validation issues. * Ensure documentation is completed accurately and in compliance with industry standards. * Support regulatory audits and inspections. Requirements: * Bachelor’s degree in engineering (mechanical, chemical, or related field) or relevant experience. * 3+ years of experience in CQV roles within the pharmaceutical or biotech industry. * Strong knowledge of GMP, FDA, and EU regulations. * Experience with process validation, cleaning validation, andequipment qualification. * Excellent problem-solving and communication skills. Please send your CV by