QC Sampler
Roles & Responsibilities
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
Tell employers what skills you have
Sampling
Quality Control
Materials Inspection
Hygiene
Sourcing Raw Materials
Contamination Control
Weight
Non-Conforming
Specification of Equipment
Control Systems
Safety and Environmental
Packaging Materials
Sample Management
Labeling items
Batch Management
Laboratory Methods