Senior CIP/SIP CQV Validation Engineer

Validation & Engineering Group, Inc. in Puerto Rico seeks a highly skilled Validation Specialist for CIP/SIP in a biotech manufacturing environment. You will plan, coordinate, and execute CQV activities to ensure cleaning and sterilization systems meet GMP, FDA, EMA, and ASTM E2500 standards. Collaborating with Automation, Process Engineering, and QA Validation, you will generate validated documentation, approve IOQ/PQ, and support process validation batches and cleaning validation campaigns,