MES Validation Specialist (Syncade) - GMP Biologics

A leading services supplier in the biotechnology sector seeks a Senior Computer System Validation Specialist to support a biologics manufacturing facility. The candidate will lead CSV activities for Manufacturing Execution Systems (MES), specifically Syncade. Responsibilities include development of validation documents and ensuring compliance with FDA and EMA guidelines. Candidates should have 7-10+ years of experience in CSV within GMP environments and expertise in MES Syncade validation. Excellent communication and technical writing skills are essential. #J-18808-Ljbffr