Supervise and control the mixing and manufacturing process in compliance with approved Batch Manufacturing Records and GMP standards to ensure product quality, minimize waste, and achieve the daily production plan.- Review and execute Batch Manufacturing Records (BMR) and ensure availability and verification of raw materials before production.- Ensure GMP compliance including line clearance, area cleanliness, and adherence to approved SOPs.- Monitor mixing operations, material addition, filtration, and machine performance to ensure process accuracy and efficiency.- Verify raw materials (weight, QC status, physical condition, expiry) and initiate deviation/CAPA procedures when required.- Ensure accurate documentation in line with GDP and submit completed BMRs to Quality Control on time.- Monitor machine downtime, waste percentage, and production performance; prepare daily and monthly reports.- Supervise operators’ performance, enforce PPE and safety compliance, and coordinate with Planning, QC, Engineering, and Warehouses to achieve production targets. - Bachelor’s degree in Pharmacy, Science, or related field.- 2 - 4 years of manufacturing experience, preferably in pharmaceutical or cosmetics industry.- Good knowledge of GMP, GDP, and ISO standards.- Experience with ERP systems (Oracle preferred).- Strong leadership and reporting skills.