GMP QA Intern — Documentation & Compliance

Sanofi

Singapore

On-site

SGD 18,000 - 24,000

Part time

14 days+
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

Sanofi Jurong seeks a Quality Assurance Intern to collaborate with cross-functional teams on GMP documentation lifecycle. You will bridge quality systems and site operations to ensure compliant GMP documentation at the Jurong site.

You will support audits, procedures drafting, KPI reporting, and document management while contributing to simplification and digitalization efforts within global documentation initiatives.

Qualifications

  • Hands-on exposure to GMP documentation lifecycle and quality systems.

Responsibilities

  • Support to maintain quality agreements and technical specifications with Third Parties outlining quality expectations and responsibilities.
  • Support site inspection readiness activities during internal audits and regulatory inspections (FDA and HSA).
  • Draft and update procedures, generate reports and metrics related to compliance activities; monitor monthly KPI.
  • Manage the GMP documentation lifecycle (creation, revision, obsolescence).
  • Collaborate with departments to ensure content meets business needs and processes.
  • Ensure documentation content complies with regulatory requirements and company standards.
  • Keep documentation lean, avoid redundancies and duplication.
  • Ensure accuracy, completeness and writing quality (clarity/grammar).
  • Collect needs for documentation changes, prioritize and manage updates.
  • Support implementation of documentation processes with global simplification, harmonisation and digitalization.

Skills

Quality Assurance
Documentation
Regulatory compliance
GMP
Inspection readiness
KPI reporting

Job description

Sanofi Jurong seeks a Quality Assurance Intern to collaborate with cross-functional teams on GMP documentation lifecycle. You will bridge quality systems and site operations to ensure compliant GMP documentation at the Jurong site.

You will support audits, procedures drafting, KPI reporting, and document management while contributing to simplification and digitalization efforts within global documentation initiatives.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

GMP Documentation & Compliance Intern
GMP Documentation & Compliance Intern

Sanofi Aventis Singapore Pte. Ltd • Singapore

On-site
SGD 22,000 - 33,000
Quality Assurance Intern
Quality Assurance Intern

Sanofi • Singapore

On-site
SGD 18,000 - 24,000
Quality Assurance Intern
Quality Assurance Intern

Sanofi Aventis Singapore Pte. Ltd • Singapore

On-site
SGD 22,000 - 33,000
Quality Systems Intern: Compliance & Data Integrity
Quality Systems Intern: Compliance & Data Integrity

Sanofi • Singapore

On-site
SGD 10,000 - 17,000
GMP-Focused Reliability & Compliance Intern
GMP-Focused Reliability & Compliance Intern

Sanofi Aventis Singapore Pte. Ltd • Singapore

On-site
SGD 17,000 - 26,000
Global Regulatory Affairs Intern: Compliance & Documentation
Global Regulatory Affairs Intern: Compliance & Documentation

Sanofi • Singapore

On-site
SGD 17,000 - 21,000
GMP Reliability Engineer Intern: Compliance & QA
GMP Reliability Engineer Intern: Compliance & QA

Sanofi • Singapore

On-site
SGD 20,000 - 31,000
Quality Operations Specialist II – GMP Site Support
Quality Operations Specialist II – GMP Site Support

Sanofi • Singapore

On-site
SGD 90,000 - 150,000
Quality Systems Associate — GMP & Compliance (Training Provided)
Quality Systems Associate — GMP & Compliance (Training Provided)

Manpower Singapore • Singapore

On-site
SGD 25,000 - 42,000
Regulatory Affairs Intern: Global Compliance & Inspections
Regulatory Affairs Intern: Global Compliance & Inspections

Sanofi Aventis Singapore Pte. Ltd • Singapore

On-site
SGD 15,000 - 18,000