GMP Documentation & Compliance Intern

Sanofi Aventis Singapore Pte. Ltd; Singapore; On-site; SGD 22,000 - 33,000; Full time

Job summary

Sanofi Jurong is seeking a Quality Assurance Intern to support GMP documentation lifecycle across cross-functional teams, ensuring compliance with site standards. You will assist with quality agreements, audit readiness, procedure drafting, KPI reporting, and maintenance of documentation content in collaboration with QA, regulatory, and operations.

This role offers exposure to global documentation initiatives and a chance to develop hands-on skills in quality systems within a leading

Responsibilities

• Maintain GMP documentation lifecycle (creation, revision, obsolescence)
• Assist inspection readiness during internal audits and regulatory inspections (FDA, HSA)
• Draft and update procedures; generate reports and KPIs for compliance monitoring
• Collaborate with departments to ensure documentation meets business needs
• Ensure content compliance with regulatory requirements and company standards
• Keep documentation lean, avoiding redundancies and duplication
• Ensure documentation accuracy, completeness, and writing quality
• Collect and prioritize documentation change requests
• Support global documentation initiatives focusing on simplification, harmonisation, and digitalization

Job description

Sanofi Jurong is seeking a Quality Assurance Intern to support GMP documentation lifecycle across cross-functional teams, ensuring compliance with site standards. You will assist with quality agreements, audit readiness, procedure drafting, KPI reporting, and maintenance of documentation content in collaboration with QA, regulatory, and operations.

This role offers exposure to global documentation initiatives and a chance to develop hands-on skills in quality systems within a leading