Validation Engineering Intern
About this opportunity
Location: Waterford, Ireland
Start date: January 2027
Duration: 6 to 8 months
Work Model: full time, onsite
About the job
Join our Commissioning and Qualification team in Waterford and gain hands-on experience in pharmaceutical manufacturing. As a Validation Engineering Intern, you will support equipment qualification activities, help ensure quality and compliance standards are met, and work alongside experienced engineers on projects that directly support the manufacture of medicines.
This internship is designed for students completing a mandatory university placement as part of their degree program.
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:
Support the preparation and review of equipment qualification protocols and documentation.
Assist with qualification testing and data collection activities on manufacturing and packaging equipment.
Record observations, test results, and findings accurately following quality requirements.
Help prepare reports and validation records for review and approval.
Support equipment inspections and readiness checks before qualification activities.
Assist with compliance-related documentation and continuous improvement initiatives.
Collaborate with engineering, manufacturing, and quality teams to support validation projects.
About you
To excel in this role you will need:
To be currently enrolled in a university degree programme, with the internship forming a mandatory part of your studies.
A background in Chemical, Mechanical, Electrical, Pharmaceutical Engineering, or a related technical discipline.
Strong attention to detail and the ability to follow procedures and maintain accurate documentation.
Good written and verbal communication skills in English.
A collaborative approach and the ability to work effectively with different teams.
Curiosity, a willingness to learn, and an interest in pharmaceutical manufacturing and engineering.
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.
Explore more with personalized development plans, short-term gigs, and internal mobility across functions and countries.
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 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 !
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 420 comparable Intern/Fellow/Postdoc Manufacturing & CMC roles across 58 biopharma companies.
Salary context
93 of 420 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 420 comparable roles
+ 20 more countries
Seniority mix
420 of 420 peers have a known seniority level
Therapeutic area mix
6 of 420 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.