Regulatory Affairs Intern 6 Months H/F - Nemera

With sales of €700m and 3,300 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.

Regulatory Affairs Intern

(6 months - March 2027 - Lyon)

We are looking for our new Regulatory Affairs Intern for a duration of 6 months, based in Lyon.

As a Regulatory Affairs Intern, you will support the Regulatory Affairs team in ensuring regulatory compliance of medical devices and combination products throughout their lifecycle. You will work closely with Regulatory Affairs Project Managers and interact with Quality, Design, Project Management, Manufacturing, and other cross-functional teams.

This 6months internship offers a unique opportunity to gain exposure to global medical device regulations and to participate in strategic regulatory projects within an international environment.

Missions:

• Support the preparation, maintenance and organization of regulatory documentation throughout the product lifecycle.
• Perform document gap assessments and collect, consolidate and verify regulatory data.
• Monitor regulatory and standards updates and assess their potential impact.
• Update regulatory documentation following product changes.
• Support the evaluation of new regulatory requirements and technical change impacts.
• Prepare regulatory summaries, reports and presentations.
• Assist Regulatory Affairs Project Managers in coordinating regulatory activities and projects.
• Track project actions, maintain trackers and follow up on regulatory deliverables.
• Participate in cross-functional meetings and prepare meeting minutes and status updates.
• Support compliance and continuous improvement initiatives within Regulatory Affairs.
• Contribute to responses to customer, authority and internal regulatory requests.
• Assist with audit preparation and follow-up of corrective actions.
• Maintain regulatory databases and document management systems.
• Collaborate with cross-functional teams to ensure regulatory compliance and timely project execution.

• Master's degree student (Bac +4/Bac +5) in, Regulatory Affairs, Biomedical Engineering or Pharmaceutical Sciences
• Or Experience in medical devices or pharmaceuticals or combination device
• Attention to detail and rigor, Curiosity and willingness to learn.
• Good analytical and organizational skills.
• Fluent English & French.
• Autonomous, proactive, and solution-oriented mindset.
• Ability to work in a multicultural and cross-functional environment.