Internship - Quality - Regulatory Engineer M H/F - 69

With sales of €600m and 3000 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has built very long lasting, strong relationships with the leading global pharmaceutical companies globally by providing high quality development, industrialization and manufacturing services. Nemera develops and manufactures its own IP product platforms but also offers also fully custom developments and contract manufacturing.

Nemera's manufacturing sites are located in the US, France, Germany, Brazil and Poland. The headquarters and Innovation Center for early device design and development are located in France (Lyon).

We have big ambitions at Nemera! We are growing our franchises and strengthening our capabilities.Location: Nemera - Lyon Gerland Site
Field: Medical Devices
Duration: 6 months

Join Nemera, a global leader in medical device solutions, and take part in a strategic project focused on a vaginal applicator produced at our Jaguariúna (Brazil) site.
Within the Parenteral & ICO unit, you will support the Quality department in building key regulatory and technical documentation for this device.

Your Mission

Working closely with design, regulatory, laboratory, and project teams, you will:

- Develop and structure the Design History File, risk management file, and Technical File for the product.
- Ensure proper traceability of project requirements and documentation, coordinating with all project stakeholders.
- Lead and support risk management activities.
- Challenge and assist the design team throughout their activities.
- Provide regular activity updates to the Quality Project Manager.