Quality Associate

Sanofi is hiring a Quality Associate in Seoul, South Korea. Level rates it ; you can apply on Sanofi.

Level's read on this job

On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
Tools and skills the posting cites include quality assurance, gmp and deviation handling.
Level classifies it as a mid-level role.
Level lists 1,000+ other open roles at Sanofi.

AI in this role

Manage quality assurance, product technical complaints, and compliance activities in a temporary role at Sanofi.

quality-assurancegmpdeviation-handlingcaparegulatory-compliance

Job title: Quality Associate

● Location: Seoul, South Korea

* This is a 1.5 year temporary position.

About the job

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

Manage product technical complaints, monitor investigation activities, and follow up on outcomes to ensure timely resolution.
Handle quality events, including deviations, change controls, and CAPA activities.
Coordinate and support analytical method validation and transfer activities to ensure timely and successful implementation.
Maintain quality agreements with manufacturing sites and third-party suppliers of products and reference standards.
Support product release activities in compliance with local regulatory requirements and company quality standards.
Maintain quality documentation and training records, ensuring they remain accurate and up to date.
Support the delivery and tracking of GMP and quality-related training activities across the team.
Support quality audits and inspections, including self-inspections, MFDS overseas GMP inspections, MFDS GIP inspections, and health authority inspections.
Follow up on inspection observations and corrective and preventive actions (CAPAs) to ensure timely closure.
Liaise with local health authorities regarding quality-related regulatory requests and commitments.
Serve as backup for Annual Product Quality Review (APQR) activities.

About you

Experience: Background in pharmaceutical quality assurance, quality control, or regulatory affairs(2-5 years of relevant experience required)
Soft and technical skills: Strong attention to detail, analytical thinking, and familiarity with GxP quality systems and complaint/deviation handling processes; able to work independently and collaboratively across cross-functional teams
Education: Degree in Pharmacy, Chemistry, Life Sciences, or a related field
Languages: Professional proficiency in English for collaboration with global teams

Why choose us?

Help shape the future of care for chronic and complex conditions like aT1D, Type 2 diabetes, transplant, and cardiovascular disease.
Drive meaningful impact at global scale: our medicines reach more than 100 million people each year.
Be part of a simpler, digital- and AI-powered business that’s rethinking how we work and engage with the world.
Turn bold ideas into breakthrough launches, with multiple new therapies planned through 2030 and beyond.
Stretch your career in a development playground, with opportunities across functions, regions, and the entire product lifecycle.

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!

How we rate this

Quality Associate at Sanofi rates 0 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.

Classification

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.

Key facts

Quality Associate is an open job at Sanofi.
Level rates this role AI Level 1 of 4: Little AI.
The role is based in Seoul.
The job was posted on October 2, 2026.
Seniority: mid.
Applications are handled by Sanofi. Apply on Sanofi

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Quality AssuranceGmpDeviation HandlingCapaRegulatory Compliance

Questions you could be asked

Tell me about a project where quality assurance was part of your work. What did you do?
Tell me about a project where gmp was part of your work. What did you do?
Tell me about a project where deviation handling was part of your work. What did you do?
Tell me about a project where capa was part of your work. What did you do?
Tell me about a project where regulatory compliance was part of your work. What did you do?

Adapt your resume

List these exact terms on your resume: Quality Assurance, Gmp, Deviation Handling, Capa, and Regulatory 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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