Quality Assurance Executive

DCH AURIGA SINGAPORE; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading distribution company based in Singapore is seeking a Quality Assurance Executive to ensure compliance and quality of processes and products. The role involves implementing quality control systems, conducting inspections, and introducing process improvements. Candidates should hold a Diploma or Bachelor's degree and ideally have ISO certification. Both experienced individuals and fresh graduates are encouraged to apply. Strong problem-solving and communication skills are essential.

Qualifications

• Minimum 1-2 years in Quality System & Assurance or GMP/GLP is advantageous.
• Fresh candidates are encouraged to apply.

Responsibilities

• Ensure secondary assembly operations per SOP and GMP guidelines.
• Create Master Batch Packaging Record for Non-Pharmaceutical Products.
• Perform Incoming Quality Inspection for Pharmaceutical Trade Returned Products.
• Report and follow-up on non-conforming products.

Skills

Effective problem-solving skills

Strong interpersonal skills

Communication skills

Education

Diploma or Bachelor's degree

Certification in ISO 9001 and ISO 13485

Job description

As the Quality Assurance Executive at DCH AURIGA SINGAPORE, you will play a crucial role in ensuring the quality and compliance of our processes and products. This full-time position, based in the Distribution Center, is responsible for implementing and maintaining our quality control systems to meet the highest industry standards.

Job Responsibilities

• Ensure secondary assembly operations performed per SOP and PIC/S GMP applicable guidelines.
• Ensure sufficient PPM inventory level to ensure no disruption to secondary assembly operations.
• Responsible in creating Master Batch Packaging Record (MBPR) for Non-Pharmaceutical Products.
• Introduce process improvement relevant to second assembly operations.
• Housekeeping of redressing area.
• Responsible in performing 100% Incoming Quality Inspection for Pharmaceutical Trade Returned Products.
• Responsible in performing Sampling Incoming Quality Inspection & reporting based on Principal Artwork (as per Technical Agreement).
• Responsible in reporting and follow-up on non-conforming products (Inclusive of Incoming, Outgoing, Returns, 3PL and Redressing).
• Responsible in Reporting, monitoring and closing of Customer Complaints.
• Responsible in monitoring and verification of warehouse temperature and Humidity Records.

Qualifications

• Diploma or Bachelor's degree. Preferably with certification in ISO 9001 and ISO 13485 standards.
• Preferably minimum 1-2 years of experiences in Quality System & Assurance or GMP / GLP will be advantageous.
• Fresh entry are encouraged to apply.
• Effective problem-solving skills with a continuous improvement mindset.
• Strong interpersonal and communication skills to collaborate effectively across functions and levels.

Only shortlisted candidates will be notified.