QC System Administrator Trainee (CCP)

October 28, 2026

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Job Title: QC System Administrator Trainee (CCP)

Location: Singapore / Tuas

About the Job

The Career Conversion Programme (CCP) (Train-and-Place) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry in anticipation of hiring demand. This programme is jointly supported by the Workforce Singapore (WSG) and Workforce Advancement Federation (WAF).

The training programme consists of 15 months of local attachment at Sanofi (Aventis-Pharma). Only candidates eligible for CCP programme may apply.

Our Company:

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s life. We turn the impossible in to the possible by discovering, developing and delivering medicines and vaccines for millions of people around the world.

The Sanofi Modulus is at the cornerstone of our strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable and agile, leveraging new disruptive technologies, to better address biologics business challenges.

In this context, we are looking for one Quality Control System Administrator Trainee (Career Conversion Program) to support in the setting up and maintenance of QC laboratory system administrative activities.

Main Responsibilities:

The candidate will have a routine operational role consisting of the following:

Supporting local deployments of QC digital solutions (core model and local), in accordance with defined deployment plans and validation protocols.

Issuing local documentation related to QC digital solutions in scope, required to ensure their usage and maintenance in an appropriate way.

Providing training and support of end-user on QC digital tools.

Maintaining and updating master data and end-user access to the QC digital tools, according to defined requirements and documentation.

Supporting the execution of qualification related to QC equipment (eg. Write protocol, risk assessment, report) to ensure adherence to the committed scheduled plans.

Contribute to the compliance of laboratory GXP asset qualification and maintain with applicable regulatory requirements and quality standards.

Informing his/her manager of any event related to digital systems in scope in a timely manner to ensure investigation and impact assessment are performed appropriately, participate actively in investigation, execute assigned CAPA related to remediation or mitigation plans.

Continuous Improvement: Identify and contribute to process optimization opportunities within the QC laboratory.

About You

Diploma or Degree in Pharmaceutical Sciences, Applied Science or related life Sciences disciplines.
Candidate with prior internships or industrial attachments in biopharmaceutical and biotechnology organizations would be advantageous.

Self-starter and independent worker who can operate and perform in cross functional teams.

Possess strong analytical and critical thinking skills with the ability to problem solving and navigate through complexity and ambiguity.

Able to work in fast paced and dynamic conditions with tight timelines.

Why choose us?

.

Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
Power industry-leading performance by leveraging digital, data, and AI-driven innovation at speed and scale.
Transform lives worldwide by delivering life-changing treatments anywhere, anytime.
Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.
Work with AI, robotics, and next-gen automation to redefine global manufacturing and supply

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