QC Digital Systems Trainee — Launch Your QA Career

Sanofi Aventis Singapore Pte. Ltd; Singapore; On-site; SGD 30,000 - 42,000; Full time

Job summary

Sanofi Aventis Singapore Pte. Ltd seeks a Quality Control System Administrator Trainee as part of a Career Conversion Program to support setup and maintenance of QC laboratory digital systems.

You will assist in deployment, documentation, and user training while ensuring master data integrity and secure access. The role emphasizes compliance with GXP standards and continuous improvement in a fast-paced biopharma environment.

Qualifications

• Diploma or degree in Pharmaceutical Sciences, Applied Science or related life sciences.
• Internships or industrial attachments in biopharma/biotech advantageous.
• Self-starter and independent with cross-functional teamwork.
• Strong analytical and critical thinking with problem solving.

Responsibilities

• Support local deployments of QC digital solutions per deployment plans and validation protocols.
• Issue local documentation related to QC digital solutions to ensure proper usage and maintenance.
• Provide training and end-user support on QC digital tools.
• Maintain and update master data and end-user access to QC digital tools.
• Support execution of qualification related to QC equipment (e.g., write protocol, risk assessment, report).
• Contribute to compliance of laboratory GXP asset qualification and regulatory requirements.
• Inform manager of events related to digital systems and participate in investigations and CAPA.
• Identify opportunities for process improvement within the QC laboratory.

Skills

Analytical thinking

Critical thinking

Problem solving

Cross-functional teamwork

Education

Pharmaceutical Sciences degree

Job description

Sanofi Aventis Singapore Pte. Ltd seeks a Quality Control System Administrator Trainee as part of a Career Conversion Program to support setup and maintenance of QC laboratory digital systems.

You will assist in deployment, documentation, and user training while ensuring master data integrity and secure access. The role emphasizes compliance with GXP standards and continuous improvement in a fast-paced biopharma environment.