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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
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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
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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
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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
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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
