Production Compliance Associate - MBR Creation and Document Management | Mitarbeiter Produktions-Compliance - MBR-Erstellung und Dokumentenmanagement (alle Geschlechter)

Job Summary

This role involves ensuring high standards of pharmaceutical production compliance at Bayer's Weimar facility. As a Production Compliance Associate, your day-to-day responsibilities include creating and managing Manufacturing Batch Records (MBRs) within the Manufacturing Execution System (MES), as well as developing machine recipes and product quality reviews for bulk production. You will be a key player in document management, handling Change Requests (MOC), and maintaining GMP-compliant documentation such as SOPs and risk analyses. This position is ideal for detail-oriented professionals with a background in pharmaceutical manufacturing who enjoy a mix of technical documentation and process coordination. Joining Bayer offers the chance to work for a global leader in healthcare, providing a meaningful career path with a focus on diversity, sustainability, and professional development. The role is initially offered as a 2-year fixed-term contract with an attractive compensation package including holiday and Christmas bonuses.