CIP/SIP Validation Specialist — Biotech CQV Expert

Posted yesterday

pinnaqlBarceloneta (PR)

Validation Engineers Biological Product (except Diagnostic) Manufacturing

SENIORITY

Senior

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About the role

Validation & Engineering Group, Inc. seeks a seasoned Validation Specialist for CIP/SIP in a biotech manufacturing setting. You will plan, coordinate, and execute CQV activities, ensure compliance with GMP, FDA/EMA, and ASTM E2500, and drive data integrity across validation programs. Requires 7–10 years CQV experience, bilingual English/Spanish, and strong collaboration with Engineering, QA, and Manufacturing teams. On-site position with extended hours as needed.

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