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