MES Validation Lead - Electronic Batch Records

Amaris Consulting in Singapore is seeking a MES Validation Specialist to support validation activities for Electronic Batch Record systems. The role involves reviewing validation packages, ensuring compliance with GMP and data integrity requirements, and collaborating with various teams. The ideal candidate should have experience in MES validation in pharmaceutical or biotech sectors, familiarity with EBR validation, and an academic background in engineering or life sciences.
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