Quality Interm

About Us 

Opella, the Consumer Healthcare business unit of Sanofi, is the purest and third-largest player globally in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market.    

We have an unshakable belief in the power of self-care and the role it can play in creating a healthier society and a healthier planet.  

That's why we want to make self-care as simple as it should be by being consumer-led always, with science at our core.   

Through our unique and balanced portfolio of more than 100 loved brands, including 15 global and local high-growth challengers such as Allegra, Dulcolax and Buscopan, we deliver our mission: helping more than half a billion consumers worldwide take their health in their hands.    

This mission is brought to life by an 11,000-strong team, 13 best-in-class manufacturing sites, and 4 specialized science and innovation development centers.   

We are also proud to be the first major fast-moving consumer healthcare company to achieve B Corp certification.   

Join us on our mission. Health. In your hands. 

Within the International Opella EM CHC EULA department, you will join a dynamic team committed to continuous improvement in drug product and process quality. This internship offers a unique opportunity to explore quality-related challenges in an international and multicultural environment.

About the role

As an intern, you will actively contribute to the department's quality activities. Your main tasks will include:

• Supporting the implementation and monitoring of quality processes in line with internal standards and regulatory requirements.

• Participating in the analysis of quality data and helping to identify improvement actions.

• Collaborating with local and international teams to ensure product and process compliance.

• Assisting in the management and updating of quality documentation (procedures, jobs aids, reports).

• Contributing to cross-functional continuous improvement projects.

About you:

• You have experience/knowledge in the pharmaceutical industry.

• You have gathered experience on the field of quality.

• You have worked in a GMP environment.

• Any experience with medical devices or with VMS is a great plus.

• You speak English on a fluent level, French language is an advantage.

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