Senior Validation Engineer

Role: Quality Assurance Specialist focusing on validation activities within pharmaceutical manufacturing. Objectives: ensure compliance of validation master plans, protocols, and reports; troubleshoot validation issues; support quality systems and regulatory audits. Responsibilities: review and approve validation documentation, conduct data analysis for investigations, manage change controls, and support product transfers and new development projects. Qualifications: high school diploma with 8+ years, associate's with 6+ years, or BA/BS with 2+ years in GMP environments; strong knowledge of quality systems, validation, and pharmaceutical processes. Preferred skills include experience with sterile products, medical devices, and regulatory audits, along with familiarity with AI tools. High-Value: validation, GMP compliance, pharmaceutical manufacturing, sterile products, regulated environment, validation master plan, investigations, regulatory audits. Work setup: on-premise manufacturing site with occasional non-standard hours, minimal travel.