About this opportunity
Syner-G BioPharma Group lists this Senior Validation Engineer — GMP/CSV & MES Expert opportunity in northern, Kentucky. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Syner-G BioPharma Group in the United States seeks a Senior Validation Engineer (QAV) with 4‑15 years of experience to support validation across equipment, utilities, facilities, computerized systems, manufacturing processes, and MES/eBR in GMP environments.
You will develop, execute, review, and maintain validation lifecycle documentation, ensuring regulatory compliance, data integrity, and alignment with GMP requirements while collaborating with cross-functional teams for system releases and
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.