Biologics Documentation Lead - GMP & eQMS (12-Month)

Quanta Consultancy Services Ltd is seeking a Technical Writer for a 12-month contract in Cork, Ireland. You will lead and maintain the GMP documentation program, creating and approving SOPs, BPDs, and related records to ensure inspection readiness.

Ideal candidates have a life sciences background, strong regulatory knowledge (GMP/GxP), and experience with eQMS/LMS tools such as Veeva QualityDocs and ComplianceWire. Collaboration with cross-functional SMEs is essential.