XDC QC RM Sampler for QC operation

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

Job summary

A leading pharmaceutical company in Singapore is seeking a Quality Control professional to collect and inspect samples of raw materials, ensuring adherence to strict SOPs and regulatory requirements. Candidates must have strong attention to detail, good documentation skills, and the ability to work independently. This full-time position requires on-site work, offering a critical role in maintaining quality standards within the organization.

Qualifications

• Strong attention to detail and accuracy is crucial.
• Good documentation and communication skills are necessary.
• Ability to work independently and collaborate in a team environment.
• Basic computer skills for data entry and record keeping.

Responsibilities

• Collect samples of raw materials and excipients according to SOPs.
• Perform visual inspections on incoming materials for defects.
• Label, weigh, and properly store samples.
• Document all sampling activities and complete necessary paperwork.
• Clean and maintain sampling tools and work areas.
• Prepare and deliver samples to the laboratory for analysis.
• Ensure compliance with GMP and regulatory requirements.
• Report non-conforming materials or sampling issues.

Skills

Attention to detail

Good documentation skills

Communication skills

Ability to work independently

Basic computer skills

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.

Other special requirements:

• 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.
• Full time on-site work requirements