Validation Engineering Intern

Sanofi; France; On-site; EUR 12,000 - 19,000; Full time

Job summary

Sanofi in Waterford, Ireland seeks a Validation Engineering Intern to support equipment qualification activities and help ensure quality and compliance in pharmaceutical manufacturing. The role offers hands-on experience with experienced engineers on projects that directly support medicines production.

This internship is designed for students completing a mandatory university placement as part of their degree program.

Qualifications

• Background in Chemical, Mechanical, Electrical, Pharmaceutical Engineering or related technical discipline.

Responsibilities

• Support equipment qualification protocols and documentation.
• Assist qualification testing and data collection on manufacturing/packaging equipment.
• Record observations and results, ensuring quality requirements are met.
• Help prepare validation reports and records for review.
• Support inspections and readiness checks before qualification activities.
• Assist with compliance documentation and continuous improvement initiatives.
• Collaborate with engineering, manufacturing and quality teams on validation projects.

Job description

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 personalised 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 !