LEO Pharma GmbH
19.10.2025
Neu-Isenburg, Offenbach/Main
manufacturing sites • Deliver local quality intelligence to global function related to GMP/GDP requirements and new legislation in the market • Monitor quality aspects of warehousing and shipping practices for compliance with
Daiichi Sankyo Europe GmbH
25.05.2026
München
relevant experience in the pharmaceutical industry, including: • At least two years in Quality Assurance and/or Quality Management, preferably in Shop Floor QA activities or QA Oversight for GMP operations • At least two
Daiichi Sankyo Europe GmbH
10.10.2025
München
. • Serve as the Regional Business Process Owner for GMP/GDP Quality Assurance processes related to Complaint Management and Recall within the EUCAN region. • Lead the regional standardization and harmonization of Complaint
Daiichi Sankyo Europe GmbH
13.10.2025
München
, and regulatory compliance aligned with both regional and global requirements. • Act as the Regional Business Process Owner for GMP/GDP Quality Assurance processes related to Change Control and Risk Management within the
Daiichi Sankyo Europe GmbH
01.06.2026
München, Pfaffenhofen/Ilm
solutions for quality management processes. • Demonstrated experience in successfully leading complex projects. • In-depth knowledge of GMP and GDP regulations, specifically related to GxP document management. • Strong