Astellas Pharma, located in Westborough, Massachusetts, is seeking a Principal Validation Engineer to lead site validation strategies and lifecycle execution. The ideal candidate has at least 10 years of validation engineering experience in a GMP environment and a proven track record of supporting regulatory filings.
This role involves collaboration with cross-functional teams, management of validation service providers, and oversight of regulatory documentation. The position offers a comprehensive benefits package including health insurance and generous paid time off.
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