SanofiQC System Administrator Trainee (CCP)
Sanofi is hiring a QC System Administrator Trainee (CCP). Level rates it ; you can apply on Sanofi.
Level's read on this job
- Little AI ●○○○ is how Level rates this role: aI is not part of the work.
- The posting mentions gxp, quality control and system administration among its tools and skills.
- Level classes it as a junior role.
- Sanofi has 953 other open roles on Level.
- Posted within the past two weeks.
AI in this role
Support QC laboratory system administrative activities, deployments, and compliance in biopharmaceuticals manufacturing.
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
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!
How we rate this
QC System Administrator Trainee (CCP) at Sanofi rates 10 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where gxp was part of your work. What did you do?
- Tell me about a project where quality control was part of your work. What did you do?
- Tell me about a project where system administration was part of your work. What did you do?
- Tell me about a project where documentation was part of your work. What did you do?
- Tell me about a project where compliance was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Gxp, Quality Control, System Administration, Documentation, and Compliance. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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