Kyowa Kirin, Inc.- U.S.

Bachelor's degree in finance, Business Administration, Accounting, Life Sciences, or related discipline required. Minimum 7 years of experience in clinical trial budgeting, site financial management, or global clinical business operations

PhD preferred, 10+ years pharmaceutical industry experience, understanding of MIDD strategies

Bachelor's degree in life sciences, pharmacy, or a related scientific discipline; 12+ years of regulatory affairs experience; proven leadership experience

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

Bachelor’s degree, 10+ years of experience, and strong background in audit/inspection readiness, CAPA management, and vendor oversight

5+ years of pharmaceutical sales experience, 3+ years of pharmaceutical account management experience, 3+ years of experience within institutional, oncology, or rare disease sales

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

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

Bachelor’s degree or equivalent experience in computer science, information systems, engineering or related fields required. 8+ years of experience in the configuration, implementation, support and operations of Veeva Vault-based solutions

2+ years of experience in a GxP regulated environment, with a focus on batch record review, batch disposition, Shop Floor QA, Manufacturing Quality Assurance, and/or Incoming Quality Assurance