Quality Control Chemist - cGMP & Method Validation

Morgan McKinley is assisting a leading pharmaceutical manufacturer in Tipperary to hire a Quality Control Analyst. The role focuses on preparing the lab for full operation, performing analytical testing, and supporting method validation and transfers.

Ideal candidates have 3-5 years in a cGMP QC environment, hands-on HPLC/GC experience, and solid GDP/cGMP knowledge to ensure regulatory compliance and audit readiness.