Conduct incoming material QC check as per Acceptable Quality Limits (AQL) plan and Standard Operating Procedure (SOP)
Assist to track and update external QC lab testing status and report documentation for raw materials, excipients and finished products in Production-QC tracker
Conduct batch release documentation according to established specifications and requirements of raw materials and finished product to ensure commercial order fulfilment
Assist to track and update Stability Studies reports status to provide support to product Stability Studies program.
Provide support in QC testing invoice verification prior to submission for finance processing.
Provide support in QC systems improvement and development according to cGMP and Pharmacopeia standards.
Ensure smooth product release to support production planning.
Production support
Work closely with supply chain on in / out flowing goods and ensure proper inventory levels of materials
Coordinating and arranging of production / packing jobs with contract manufacturers and updating of its progress in the production tracker
Liaising with Contract Manufacturers, vendors and suppliers to prepare delivery notes and / or collection notes to facilitate stock movement
Provide support in verification of invoices from suppliers and service providers prior to submission for finance processing.
Ensure Good Distribution Practices (GDP) compliance and provide support to the department on system improvements and work processes.
Qualifications :
Higher Nitec / Diploma in pharmaceutical sciences, chemical engineering, or other chemistry-related disciplines.
Good written and verbal communication skills. (This role requires liaising with suppliers / manufacturers in China).
Good time and task management and coordination skills