QA Administrator - Manufacturing Solids | Gesundheitsmanager (m/w/d)

Daiichi Sankyo Europe GmbH

Pfaffenhofen an der Ilm, Bayern, Deutschland
Published Nov 6, 2025
Full-time
No information

Job Summary

This role is central to maintaining strict quality assurance and regulatory compliance within the Manufacturing Solids division at the Pfaffenhofen/Ilm development and production site. The QA Administrator will be responsible for the meticulous preparation and review of batch documentation both pre- and post-production, including performing the crucial QA sign-off within the S4Hana system. Key daily tasks involve verifying data transfers between paper and IT systems, controlling audit trails for IPK devices, and managing Work-In-Progress (WIP) reports. Candidates must possess successful vocational training, ideally in the pharmaceutical, health, or food sector, combined with professional experience in QA within an industrial production setting, specifically adhering to GMP conditions. This position requires strong organizational skills, reliability, and the ability to manage complex documentation processes to support the company's mission in oncology and cardiovascular health.

Required Skills

Education

Successfully completed vocational training, ideally in the pharmaceutical, health, or food industry.

Experience

  • Professional experience in QA within an industrial production operation
  • Experience, preferably in the pharmaceutical industry under GMP conditions or in the health/food industry
  • Practical experience conducting reviews of batch documentation, audit trails, and WIP reports (electronic and paper-based)

Languages

German (Fluent)English (Intermediate)

Additional

  • Primary deployment in the hygiene area.