QC Sampler

Main Responsibilities: • Collect samples of raw materials, excipients, packaging materials adhering strictly to SOPs. • Perform visual inspections on incoming materials for defects, cleanliness, and consistency. • Label, weigh, and properly store samples to maintain integrity and prevent contamination. • Document all sampling activities, including product and batch information, and complete necessary paperwork. • Clean and maintain sampling tools, equipment, and work areas. • Prepare and deliver samples to the appropriate laboratory for further analysis. • Ensure sampling is conducted in a clean, controlled, and safe environment according to GMP and other regulatory requirements. • Report any non-conforming materials or issues encountered during sampling. • Coordinate with other departments, such as Quality Assurance and Warehouse, as needed. • Responsible for the use of the following electronic system application, including but not limit to LIMS and LES. • Responsible for arrangement of sample shipment or external contract lab for testing • Ensure all the activities in QC team performed with compliance of cGMP, data integrity and EHS requirement. About You: • Diploma in Life Science, Process Technology, Pharmaceutical Sciences or equivalent. • 1-2 years of sampling experience in the pharmaceutical or medical devices industry, with experience on working in a laboratory environment preferred. • Have GMP manufacturing knowledge. • Strong attention to detail and accuracy is crucial. • Good documentation and communication skills. • Ability to work independently and as part of a team. • Basic computer skills for data entry and record keeping. Contract Duration: 12 months contract