Piper Companies is seeking a Validation Engineer (CQV) in Raritan, NJ to support a leading cell therapy organization. This role focuses on commissioning, qualification, and validation of laboratory equipment within a GMP-regulated cell therapy environment.
Responsibilities include IQ/OQ/PQ execution, CQV documentation, and ensuring equipment readiness while maintaining data integrity and regulatory alignment. This onsite, long-term contract position offers comprehensive benefits and on-site work.
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