QC Sampler

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 28,000 - 45,000; Full time

Job summary

NUSANTARA PRIME CONSULTING PTE. LTD. is seeking a Sampling Technician to perform material sampling, inspection, and documentation within a GMP‑driven lab environment in Singapore.

You will collect and inspect samples, maintain accurate records, and support QA and Warehouse teams while complying with cGMP and data integrity standards. 12‑month contract, on‑site position.

Qualifications

• Diploma in Life Science or equivalent.
• 1–2 years of sampling experience in pharma/medical devices, labs preferred.
• GMP manufacturing knowledge is expected.

Responsibilities

• Collect samples of raw materials, excipients, and packaging per SOPs.
• Perform visual inspections for defects and cleanliness of incoming materials.
• Document sampling activities with product and batch details and paperwork.
• Label, weigh, and store samples to maintain integrity and prevent contamination.
• Operate and maintain sampling tools and keep work areas clean.
• Coordinate with QA and Warehouse as needed.
• Ensure sampling complies with cGMP, data integrity, and EHS requirements.

Skills

Attention to detail

Documentation

Communication skills

Laboratory environment experience

GMP knowledge

Education

Diploma in Life Science

Tools

LIMS

LES

Job description

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