Lead CIP Validation Engineer – Biotech & GMP

Validation & Engineering Group, Inc. seeks a highly skilled Validation Specialist for CIP/SIP systems in a biotech manufacturing environment. You will plan, coordinate, and execute CQV activities to ensure systems meet GMP and regulatory standards.

Responsibilities include IOQ/PQ testing, documentation, data integrity, and cross-functional collaboration with QA, Process, Automation, and Manufacturing, with bilingual English/Spanish communication. Extended hours and weekend work may be required.