Industrial Engineer

Role: Continuous Improvement Engineer focused on optimizing pharmaceutical manufacturing processes, enhancing operational efficiency, and ensuring GMP/regulatory compliance through lean methodologies. Responsibilities: lead DMAIC projects, utilize value stream mapping, execute Kaizen events, support validation activities (IQ/OQ/PQ), analyze data with statistical tools, develop KPIs, identify cost-saving opportunities, conduct bottleneck analysis, and improve throughput and capacity planning. Qualifications: Bachelor's degree in Mechanical or Electrical Engineering (Master's preferred), 3+ years in pharma/manufacturing, strong computer skills (MS Office, SAP), Lean Six Sigma Black/Green Belt certified, knowledge of cGMP, FDA regulations, and AutoCAD. Additional: OSHA respirator fit test required. High-Value: pharma manufacturing, GMP compliance, process validation, lean/Six Sigma, capacity analysis, data-driven continuous improvement.