Led day-to-day pharmaceutical production activities to meet the plan, ensuring schedule adherence, throughput targets, and cGMP/SOP compliance.
Supervised shift operators, assigned tasks, monitored performance, and reinforced disciplined shop-floor execution and safety practices.
Executed line clearance and changeovers; verified correct materials, labels, and documentation to prevent mix-ups and cross-contamination.
Managed batch manufacturing/packaging documentation (BMR/BPR) and ensured real-time recording in line with Good Documentation Practices (GDP).
Monitored in-process controls (IPC) and critical parameters; coordinated with QA on out-of-spec results, holds, and product disposition.
Supported deviation containment and investigations; collected evidence, contributed to root-cause analysis, and followed up on CAPA implementation.
Coordinated with Maintenance/Engineering to troubleshoot breakdowns and support preventive maintenance, reducing unplanned downtime.
Tracked and reported line KPIs (output, yield,
rejects, downtime, changeover time) and proposed improvement actions.
