Required Skills: Compliance Investigations, Conflict Management, Cross-Functional Project Management, Deviation Management, Good Manufacturing Practices (GMP), Operational Quality, Project Leadership, Project Life Cycle Management, Project Risk Assessments, Quality Assurance Systems, Quality Auditing, Quality Management, Quality Oversight, Quality Risk Management, Quality Systems Compliance, Regulatory Compliance, Strategic Thinking. This position will serve an important role in supporting the expansion of clinical development activities at the site with responsibilities including, but not limited to the following: Execute GMP quality assurance activities directly related to facilities, equipment, and automation for clinical trial material supply capabilities.