S/M.S. in Science or Engineering, or related fields. 5+ years of relevant experience in supply chain management. Certification in Supply Chain Management or Project Management is a plus. Experience with inventory and Supply Chain Management for complex global clinical trials. Experience with upstream material management and device assembly is a plus. Knowledge of import/export requirements and experience with international clinical supply. Working knowledge of ICH guidelines, CFR, and EMA GMP and GDP Guidelines. Solid understanding of Good Manufacturing Practices (GMP). Proven ability to manage multiple projects and resolve issues. Ability to adapt to a fast-paced, dynamic work environment. Excellent communication and influencing skills. Strong collaboration skills. Strong knowledge of Microsoft Office (Excel, Word, PowerPoint). Smartsheet experience is strongly preferred. PowerBI, experienced excel (macros), and/or Tableau is a plus.