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.

🔎 Your Profile

• You are currently pursuing a Master’s degree (1st or 2nd year) in regulatory quality within the pharmaceutical device field.

• Strong communication skills.

• Excellent organizational abilities and attention to detail.

• Enjoy working in a multicultural, cross-functional team (regulatory, design, lab, materials, project management, etc.).

• Motivated, autonomous, and proactive.

• Very good level of English (spoken and written).

• Mandatory: Knowledge of ISO 13485.

🚀 Why Joining Us?

• Contribute to a project with high regulatory and technical impact in the medical device industry.

• Gain experience within a dynamic, international environment.

• Strengthen key skills in quality, risk management, and project documentation.

Our Recruitment Process

We believe in a transparent and straightforward recruitment process to ensure a great fit for both you and our team.
Here's what you can expect:
- CV Review: Upon receiving your CV, our Talent Acquisition Team will review it to assess your qualifications for the role.
- Initial Screening: If your profile matches our requirements, you'll be invited for an initial screening call with a member of our Talent Acquisition Team.
- Interview with Hiring Manager: After the initial screening, you'll have an interview with the Hiring Manager to discuss your experience, skills, and fit for the role in more detail.
- Offer: If all goes well, you'll receive an offer to join our team!

We look forward to receiving your application (resume submitted in English is appreciated). We offer varied jobs job in an international group, if you want to discover more about Nemera, please look at our website www.nemera.net

Know someone at Nemera? We have a Referral Program so, be sure to have them submit you as a referral prior to applying for this position!

Chez Nemera, nous valorisons la diversité et l'inclusion et nous nous engageons à créer un environnement de travail où tous les employés sont traités avec dignité et respect.
Nous sommes fiers d'être un employeur offrant l'égalité des chances et nous encourageons les candidatures de toutes les origines, genres, orientations sexuelles, âges, et capacités.