QC RM Sampler

WUXI XDC SINGAPORE PRIVATE LIMITED; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

A leading global pharmaceutical company located in Singapore is looking for a Quality Control Technician. The role focuses on collecting and inspecting raw material samples, ensuring compliance with GMP regulations, documenting activities accurately, and maintaining workspace cleanliness. Ideal candidates will have strong attention to detail, good communication skills, and basic computer skills. This position requires on-site work, offering a chance to contribute to a compliant and safe working environment.

Qualifications

• Knowledge of GMP, SOPs, and relevant regulations.
• Strong attention to detail and accuracy.
• Good documentation and communication skills.

Responsibilities

• Collect samples of raw materials and excipients.
• Perform visual inspections on incoming materials.
• Label, weigh, and store samples to maintain integrity.
• Document all sampling activities.
• Clean and maintain sampling tools and work areas.

Skills

Attention to detail

Good documentation skills

Communication skills

Ability to learn GMP and SOPs

Teamwork

Tools

LIMS

LES

Job description

• Collect samples of raw materials, excipients 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.
• Ensure all the activities in QC team performed with compliance of cGMP, data integrity and EHS requirement.

Requirements

• Knowledge of or ability to learn and follow GMP, SOPs, and other relevant regulations
• 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.
• Fulltime on‑site work requirements