Validation Engineer Sterile Pharmaceutical Production | Validierungsingenieur (m/w/d) Sterile Arzneimittelproduktion in Mannheim (1269)

Job Summary

As a Validation Engineer, you will play a pivotal role in the production and packaging of sterile pharmaceuticals. Your day-to-day responsibilities will involve managing validation and qualification processes, optimizing technical workflows, and contributing specialized expertise to the organization. This includes supporting product transfers, implementing new equipment, and enhancing existing manufacturing processes. You will plan and execute technical tests and machine trials, manage deviations, and implement change control measures. A key aspect of the role is comprehensive documentation, including creating and archiving test reports and plans in compliance with regulations. You will also serve as a technical point of contact, representing your department in interdisciplinary teams, and facilitate knowledge transfer within the company. This position offers an opportunity to drive innovation and quality in a dynamic team environment, contributing to the production of high-quality sterile medicines.