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.

Requirements

-  Bachelor’s degree in Pharmacy, Science, or related field.
-  2 - 5 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.