Quality Assurance Intern - Documentation & Compliance
Sanofi is hiring a Quality Assurance Intern - Documentation & Compliance. Level rates it ; you can apply on Level.
Level's read on this job
- On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
- The posting mentions quality assurance, documentation and compliance among its tools and skills.
- Level classes it as an internship.
- Sanofi has 984 other open roles on Level.
- This posting went up within the past week.
AI in this role
Support quality assurance documentation, batch release records, and audit preparations as an QA Intern at Sanofi.
- Location: Waterford
- Start date: January 2027
- Duration: 8 months
- Work Model: Onsite
About the job
As a Quality Assurance Intern, you will join our Quality team in Waterford and gain hands-on experience of how quality processes support the manufacture and release of medicines.
You will support documentation and archiving activities across the QA Specialist teams, help prepare records used during the batch release process, and gain exposure to quality audits, inspections and day-to-day quality operations. You will work with different systems, teams and processes, giving you the opportunity to build practical experience in a regulated pharmaceutical environment. This internship is ideal for a Life Sciences student who is organised, curious and keen to understand how Quality Assurance works within the pharmaceutical industry.
Ready to grow your skills while helping shape the future of healthcare? At Sanofi, you’ll be empowered to learn, ask questions, and bring your ideas to life – all while supported by inspiring mentors and collaborative teams.
Main responsibilities:
- Support the preparation, review and archiving of Quality Assurance documentation.
- Upload batch release documentation to internal systems and support the associated archiving activities.
- Help maintain well-organised records and working areas in line with quality and 5S standards.
- Support monthly quality audit walkthroughs and preparation activities for GMP audits and inspections.
- Take part in daily and weekly Quality team meetings, giving you exposure to how day-to-day quality operations are managed.
- Work in line with Good Manufacturing Practice requirements, Standard Operating Procedures and site safety expectations.
- Collaborate with colleagues across Quality and other departments while contributing ideas and supporting continuous improvement activities.
About you
To excel in this role you will need to have:
- Be currently studying towards a Bachelor’s or Master’s degree in Life Sciences and be returning to university after completing the internship.
- Have an interest in the pharmaceutical industry and in developing your knowledge of Quality Assurance.
- Strong attention to detail and an organised approach to your work.
- Confidence using computers and an ability to learn new systems and digital tools.
- A willingness to learn, ask questions and take initiative as your knowledge develops.
- Good communication skills and the ability to work collaboratively with colleagues across different teams.
Experience using tools such as Excel, different software platforms or technical/scientific writing as part of your studies would be helpful, but is not essential. Training will be provided on the systems and processes used in the role.
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.
Why choose us?
- Stretch your skills through apprenticeships, internships, graduate programs, and international experiences that grow with you.
- Learn from inspiring mentors and collaborative teams while contributing to real projects that shape the future of healthcare.
- Build your future with access to the latest tools, digital innovation, and continuous learning that keep you ahead of the curve.
- Grow in a purpose-driven company where your voice matters and your work helps improve millions of lives.
- Thrive in inclusive, flexible workplaces that support your personal and professional well-being.
- Launch your career with a company that invests in you — and empowers you to reimagine what’s possible.
We reserve the right to close this vacancy earlier than the advertised closing date should we receive a sufficient number of applications.
#LI-EUR #LI-Onsite
Pursue progress, discover extraordinaryBetter 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 Assurance Intern - Documentation & Compliance 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.
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. Open the description and count.
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 quality assurance 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?
- Tell me about a project where gmp was part of your work. What did you do?
- Tell me about a project where auditing was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Quality Assurance, Documentation, Compliance, Gmp, and Auditing. 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.
Want an expert to read your CV for this job?
Free. Send your CV and the role you want next. We reply by email within 2 to 4 business days.
Get new software engineering jobs by email
One email a week with the new software engineering jobs, each rated for how much AI is in the work. No recruiter spam, unsubscribe in one click.
Free. One email a week. Unsubscribe in one click.
Similar roles
Software Engineering roles that involve little AI, at other companies.
What kind of AI work fits you?
Answer 12 practical questions in about three minutes. Get a simple profile, the work it points to, and live roles to explore next.
Find my next step