A leading drug development company is seeking a Senior Validation QA Associate to ensure compliance with GXP guidelines and lead validation projects. This hybrid role requires at least 2 years of experience in Computer System Validation within a GCP or GMP environment. Strong communication and collaborative skills are essential. The position is based in Nottingham and involves maintaining documentation, supporting continuous improvement, and ensuring regulatory compliance. #J-18808-Ljbffr
Contact Detail:
Quotient Sciences Limited Recruiting Team