• Job title:Quality Control Support Summer Student

• Location:Waterford, Ireland

• Start date:1stJune2026

• Duration:3months

About the job

As aQuality Control Support Summer Student, youwillassistwith data analysis, trending, and documentation of quality control test results using laboratory information systems. You willparticipatein maintaining and preparing key quality documentation—including SOPs, batch records, and compliance reports—while also supporting regulatory activities and audits through well‑organized records and documentation. You will helpidentifyopportunities for process improvements and contribute to continuous improvement projects across quality operations. Throughout your internship, you will collaborate with cross‑functional teams and take part in training and development to strengthen your understanding of pharmaceutical quality systems.

Ready to grow your skills while helping shape the future of healthcare? At Sanofi,you’llbe empowered to learn, ask questions, and bring your ideas to life – all while supported by inspiring mentors and collaborative teams.

About Sanofi

We’rean 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:

• Assistwith data analysis, trending, and documentation of quality control test results using laboratory information systems

• Participate in quality documentation activities including standard operating procedures, batch records, and compliance reports

• Support regulatory compliance activities and quality audits by preparing documentation andmaintainingorganized records

• Contribute to process improvement initiatives byidentifyingopportunities for efficiency gains andparticipatingin continuous improvement projects

• Collaborate with cross-functional teams including Manufacturing, Regulatory Affairs, and Quality Assurance on quality-related activities

• Participate in training programs and professional development opportunities to build knowledge of pharmaceutical quality systems

About you 

To excel in this role, you will need to have:

• An ongoing degree, ideally inChemistry, Biology, Chemical Engineering, Pharmaceutical Sciences, or related scientific field.

• Basic understanding of analytical chemistry principles, laboratory techniques, and data analysis methods

• Strong attention to detail, excellent organizational abilities, and effective communication skills for working in team environments

• Self-driven mindset with a

• Demonstrated ability to follow detailed procedures accurately andmaintainhigh standardsof documentation and record-keepingproactive, can-do attitude

• Eagerness to learn about pharmaceutical quality systems, regulatory requirements, and industry best practices

• Strong teamplayer skills with excellent communication.

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 workhelpsimprove 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 reimaginewhat’spossible.

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