Sanofi

Sanofi

Posted via Workday

Quality System Management Intern

Apply by Dec 31, 2026

Posted Sep 3, 2026

Role at a glance

Salary
Not Disclosed
Location
City of Singapore, Singapore
Employment
Full-time
Experience
Previous internship or work experience in any fields
Education
Degree or Diploma preferably in a related field

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Role Summary

AI-generated

The Quality System Management Intern supports the Site Quality Department’s Quality Systems and Compliance sub-team in implementing site quality systems and compliance programs. The work spans documentation management, Quality Culture and Data Integrity initiatives, inspection readiness, and site quality projects.

What You'll Do

  • Support implementation of digital documentation solutions, and manage GMP governance and issuance of paper-bound logbooks and controlled...
  • Lead and implement a site framework and solution for document archival and destruction.
  • Support development and rollout of the onsite Quality Culture program, track quality gaps and near misses, and monitor actions in the...
  • Support logistics for internal and external inspections and the site inspection readiness program.
  • Track site Quality Projects and support identified projects.

Generated from the employer's posting. Verify important details before applying.

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Qualifications

Previous internship or work experience in any field; strong organizational and time management skills, including the ability to manage multiple tasks simultaneously; excellent written and verbal communication skills. Candidates from Polytechnic or University programmes are welcome to apply.

Preferred

  • Degree or Diploma preferably in a related field

Original job description

Content provided by the employer

About the Job

The Quality Systems and Compliance sub-team is under the remit of the Site Quality Department and is responsible for the quality system management (QMS) implementation within the site. The team is responsible for setting up or reviewing and auditing the quality management systems, third party and supplier management system, Training and Documentation systems to be used by the entire site, which is instrumental in ensuring the site systems and processes meet the international GxP requirements. The team is also responsible for the Data Integrity (DI) Program to ensure the compliance use of the digital initiatives. This includes working closely with the respective functional teams to provide oversight and guidance for data integrity and projects related to data integrity to achieve the site’s digital ambition while in compliance with data integrity requirements. Another aspect is to manage Quality Culture program, enabling the right Quality Culture to be embedded onsite. 

Documentation Management System:

  • Support the implementation of digital documentation solutions like electronic logbooks and manage the GMP governance and issuance of paper-bound logbooks on site.

  • Support the implementation of digital documentation solutions like electronic forms and manage the GMP governance and issuance of controlled printing of forms on site.

  • Lead and implement framework and solution for document archival and destruction process on site.

Quality Culture Program/ Data Integrity:

  • Support in the development and roll out the Quality Culture program onsite

  • Tracking of Quality gaps and near misses, with the use of data visualization tool to communicate stakeholders

  • Status tracking of identified actions in Data Integrity Plan

Site Inspection Readiness and Management

  • Provide support for logistics activities for internal and external inspections. Provide support for site inspection readiness program.

Quality Projects

  • Status tracking of Site Quality Projects.

  • Provide support for identified site Quality Projects.

About You

  • Degree or Diploma preferably in a related field

  • Previous internship or work experience in any fields

  • Candidates from Polytechnic or University programmes are welcome to apply

  • Strong organizational and time management skills with the ability to manage multiple tasks simultaneously

  • Excellent written and verbal communication skills

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Sanofi

About the company

Sanofi

Large Enterprise

Sanofi is a global healthcare leader committed to promoting health and well-being through the development of innovative medicines, vaccines, and therapeutic solutions. With a diverse portfolio that spans multiple therapeutic areas, including diabetes, oncology, and immunology, Sanofi is dedicated to addressing pressing health challenges and improving patient outcomes worldwide. Headquartered in France, the company employs over 100,000 individuals across more than 100 countries, fostering a culture of collaboration and scientific excellence to drive advancements in healthcare.