Hybrid Life Sciences Project Coordinator - GMP & Docs

Altuent seeks an experienced Project Coordinator with a background in Pharma, BioPharma, MedTech, or another regulated life sciences setting. You will coordinate documentation workflows, review cycles, and delivery activities, ensuring trackers, approvals, and action logs stay current.

In this permanent full-time role based in Cork with flexible hybrid working, you will support GMP documentation workflows, regulator-facing deliverables, sample shipments, and cross-functional collaboration with