QC Samplers (Pharmaceutical production/Testing/Quality /GMP)

• Responsible for the proper sampling of raw materials, intermediate products, and final drug products, ensuring compliance with Current Good Manufacturing Practices (cGMP). The role typically requires sampling for pharmaceutical production
• Sampling Operations: Perform sampling of raw materials, in-process materials, intermediate products, and finished drug products according to established, standard operating procedures (SOPs) and cGMP requirements.
• Documentation and Reporting: Accurately document all sampling activities, and promptly report any issues or deviations associated with the sampling process.
• Compliance and Safety: Ensure the sampling process meets GMP compliance, 5S standards, and Environment, Health, and Safety (EHS) requirements. Maintain a clean, safe, and organized laboratory environment.
• Coordination: Communicate effectively with the QC project team, warehouse, and production teams to ensure the smooth flow of analytical activities.
• Investigations: Assist in laboratory investigations regarding OOX (Out of X) results or deviations when necessary.
• Audits: Participate in customer audits and government inspections, promptly addressing any issues identified. 
• ITE / Diploma holder with at least two years of experience in a GMP laboratory setting.
• Understanding of pharmaceutical production, testing, quality management, and GMP regulations.

Veronica Neo Shen Hwa  - [email protected]

Personnel Reg No: R1110855

Manpower Staffing Services (S) Pte Ltd

EA Licence No: 02C3423