Pharmaceutical Technician for GMP Documentation | Pharmakant (gn) GMP Dokumentation

Job Summary

As a Pharmaceutical Technician specializing in GMP Documentation, you will play a critical role in ensuring product safety and process compliance within a leading international life sciences company. Your daily responsibilities will center on the creation, updating, and maintenance of GMP Master Batch Records (GMBRs) and Equipment/Standard Procedure documents (ESPs). You will be responsible for optimizing parameter value lists to ensure reproducible production quality and facilitate efficient batch releases. Additionally, you will support verification and validation activities through document reviews and the provision of technical data for audits. This position is ideal for a detail-oriented professional with a strong background in pharmaceutical manufacturing who thrives in a highly regulated environment. Based in the Leverkusen Chempark, this full-time role offers a structured 37.5-hour work week and the opportunity to work within a modern, innovation-driven production facility using advanced digital solutions.