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Site Sterility Steward

Lilly · Alzey, Rhineland-Palatinate

BiotechSpecialistEnglishUnspecified
GMPQA / Quality
CompanyLilly
LocationAlzey, Rhineland-Palatinate
Work modeUnspecified
LanguageEnglish
PostedMay 15, 2026
Last indexedJul 16, 2026

Job description

Embrace the opportunity to become a Site Sterility Steward and play a key role in ensuring the safety and quality of injectable medicines at our state-of-the-art facility. Leverage your expertise in sterility assurance, GMP, and microbiology to drive process excellence, regulatory compliance, and continuous improvement in a dynamic, high-tech environment. At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world wo... At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work... gmp compliance, sterility assurance, parenteral processing, microbiology, risk management, aseptic process simulation, root cause

analysis, regulatory submissions, technical writing, presentation skills, project leadership, technical mentorship, stakeholder management, facility start-up, technical transfer, quality assurance, data analysis