The posting
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



