Pharma Process Validation Engineer — Drive GMP Excellence

Job Description

Amaris Consulting is seeking a Process Validation Engineer to join our pharmaceutical manufacturing team in Singapore. You will plan, execute, and document validation activities in a GMP-regulated environment, collaborating with Manufacturing, Quality, and technical groups.

You will contribute to PPQ and CPV activities, review validation documents, assess process changes, and investigate deviations. Strong writing and analytical skills are essential, as is experience with commercial-scale

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Amaris Consulting

Pharma Process Validation Engineer — Drive GMP Excellence

Job Description

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