About this role
CQV Engineer at IPS-Integrated Project Services. Location: Dublin, Dublin, Ireland. Role: write protocols, conduct FATs, verify drawings Requirements: Bachelor of Science in Engineering; 5+ years in pharma/biotech/medical device design, construction, commissioning, validation, or QA; GMP/Validation experience. Category: Engineering Seniority: Senior Level Tools: GMP, Validation, CSV, P&IDs, QA Commitment: Full Time Workplace: Onsite Languages: English