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.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Pharmaceutical Manufacturing
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