Lead Validation Engineer, Oral Solid Dosage (Pharma)

A leading pharmaceutical services provider is seeking a Senior Validation Specialist specialized in oral solid dosage processes. The ideal candidate will have over 8 years of experience working in pharmaceutical manufacturing, ensuring compliance with validation activities in a GMP environment. Key responsibilities include developing validation protocols, executing qualification activities, and collaborating with cross-functional teams. Bilingual proficiency in English and Spanish is required, along with strong technical writing skills.
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