Design Automation Engineer

We are seeking an experienced MBR Designer to support a major pharmaceutical manufacturing project. The role focuses on design, validation, and maintenance of Master Batch Records (MBRs) in PAS-X, ensuring GMP compliance.Responsibilities:Develop, validate, and maintain MBRs.Collaborate with production, QA, and cross-functional teams.Provide training and support to end-users.Drive continuous improvement of MBR workflows.Maintain documentation and manage MBR projects.Requirements:Bachelor’s in Biotech, Pharmacy, Engineering, or related field.Proven PAS-X MBR experience.Strong knowledge of GMP and pharma regulations.Fluent German and English; excellent communication.Proficient in MS Office and MES systems.