Associate Director, Engineering

Provide overall direction to the Engineering organization including Process, Capital, Maintenance, Metrology, Utilities, and Facilities. Direct engineering teams for new product introduction, commercial, and clinical manufacturing while leading the Capital Plan and LRP. Maintain medical device production systems in an audit-ready state of compliance from initial validation through retirement. Direct GMP and non-GMP equipment, facility, and utility projects ensuring adherence to AbbVie standards. Manage multi-disciplinary teams to develop resource plans and execute facility planning, design, and projects. Lead discipline-specific engineering expertise to provide Medical Device benchmarking and quality system best practices. Develop and manage staff through hiring, performance management, and talent development. Act as the site Subject Matter Expert for medical device manufacturing, driving performance through data analysis and action plans. Own the site quality and compliance strategy, championing improvements to the quality management system.