Our client is seeking an experienced manufacturing leader to oversee a complex pharmaceutical packaging operation supporting highly automated syringe assembly, labeling, visual inspection, packaging, equipment reliability, regulatory readiness, and process improvement. This individual will provide strategic and operational leadership across a multi-shift packaging organization while improving equipment performance, throughput, changeovers, and team capability.Duties / Expectations of RoleLead packaging, visual inspection, labeling, and related operations across a multi-shift pharmaceutical manufacturing environmentDirectly oversee managers, supervisors, and an approximately 40–50 person packaging organization across three shiftsImprove performance of highly automated packaging assets, including customized syringe-connecting robotics, the Syringe Assembly Machine (SAM), labeling equipment, and the carton case packer/palletizer (CCP)Drive OEE, run-rate, downtime, changeover, scrap, and schedule-attainment improvements across packaging operationsPartner closely with Engineering to diagnose technical gaps, resolve recurring equipment failures, and restore equipment to expected performanceLead complex investigations, deviation reduction, root cause analysis, CAPAs, and GMP compliance activities related to packaging and equipment performanceOptimize packaging operations for high-mix, low-volume production, including frequent changeovers and equipment ramp-up constraintsEvaluate and develop business cases for automation, including automated visual inspection and additional future Cap ExImprove manual visual inspection processes for Paloperidone and support automation opportunities while maintaining product quality and compliancePartner with Quality, MS&T, Manufacturing, Engineering,



and other functions to ensure new equipment is fit-for-purpose and user-friendlySupport FDA inspection readiness, mock-audit remediation, and ongoing regulatory complianceDevelop managers and supervisors through coaching, accountability, performance management, and floor-level engagementMandatory RequirementsBachelor's degree in Engineering, Life Sciences, Manufacturing, or related technical discipline10+ years of pharmaceutical, medical device, or highly regulated manufacturing experienceStrong experience leading automated manufacturing, packaging, assembly, or related production operationsExperience leading managers, supervisors, and multi-shift manufacturing organizationsStrong technical background in automated equipment, process troubleshooting, and manufacturing systemsExperience managing investigations, deviations, CAPAs, root cause analysis, and GMP/compliance activitiesExperience supporting FDA inspections, regulatory audits, and inspection readinessProven success improving equipment reliability, throughput, OEE, and manufacturing efficiencyExcellent people leadership, communication, and cross-functional collaboration skillsAbility to work fully in office within a multi-shift manufacturing operationNice to HaveDirector or Senior Director-level manufacturing leadership experiencePharmaceutical packaging, sterile injectable packaging, combination product, syringe, or automated assembly experienceEngineering background with advanced equipment troubleshooting and automation expertiseHigh-mix, low-volume manufacturing experienceLean Manufacturing, Six Sigma, SMED, Continuous Improvement, or Operational Excellence experienceExperience with OEE, downtime reduction, changeover optimization, and run-rate improvementManufacturing scale-up, technology

📌 Director Of Packaging Operations (Windsor)
🏢 GForce Life Sciences
📍 Windsor