Job Description
Key Responsibilities Support IT-related applications in collaboration with the global application team and external vendors, with a strong focus on QC laboratory applications. Perform additional duties as assigned by the ITOT Director. Demonstrate strong teamwork and communication skills in cross-functional environments. Required Experience and Knowledge Minimum 5 years of experience in a pharmaceutical GMP environment. Knowledge of ITOT infrastructure and automation systems. Familiarity with common applications used in pharmaceutical manufacturing site. Understanding of Computer System Validation (CSV) concepts. Strong teamwork and communication skills. This is a 6-month contract role
