Kyowa Kirin, Inc.- U.S.

Manufacturing experience, safety and GMP compliance, collaboration with cross-functional teams

JD/LLB degree, 10 years of experience in legal and pharmaceutical industry, leading cross-functional projects and balancing conflicting demands

2 years of experience in a GxP regulated environment, Bachelor's degree in a technical or scientific discipline, and experience with start-up and operation of biopharmaceutical manufacturing processes

10+ years of experience, 4+ years of leadership experience, expert knowledge of Field Access Solutions

10+ years of progressive experience in Medical Affairs, advanced scientific or clinical degree, and strong knowledge of hematologic malignancies

Bachelor's degree in Life Science, 3+ years of experience in GCP/GLP Quality Assurance, and experience in auditing, CAPA management, and deviation review

Bachelor’s degree in life science or closely related discipline, 5-7 years of experience in Regulatory Affairs, and a proven track record as the primary regulatory reviewer for promotional and non-promotional materials

8+ years of experience implementing or supporting MS D365, expertise across multiple functional domains, and experience designing integrations between ERP and external systems

8+ years of direct industry experience in a GxP-regulated environment, Bachelor's degree in engineering or science related field