Quality Reviewer, Pharmaceutical Manufacturing | Laborant (m/w/d) als Qualitäts-Reviewer in der pharmazeutischen Fertigung

Job Summary

This critical role seeks a scientifically trained professional to manage and assure quality documentation within pharmaceutical manufacturing operations. Day-to-day responsibilities include the rigorous creation, review, and updating of essential pharmaceutical documentation, such as test specifications and Standard Operating Procedures (SOPs). The Quality Reviewer is also responsible for executing documentation control, tracking critical quality processes like complaints, CAPA measures, and Change Control requests. A key function involves performing batch releases using the ERP system and coordinating these priorities with logistics and work preparation teams. Success in this position requires very strong knowledge of GMP standards and pharmaceutical documentation requirements, coupled with excellent communication skills and a high sense of responsibility. This is an opportunity to contribute directly to process optimization and secure an unlimited contract.