Global Regulatory Affairs Intern – Medical Devices (6 months)

SmartRecruiters, Inc.; Lyon; Hybrid; EUR 7,800 - 10,000; Part time

Job summary

Nemera, headquartered in Lyon, seeks a Regulatory Affairs Intern for a 6-month placement. Based in Lyon, you will support regulatory activities across the product lifecycle and interact with quality, design, project management, and manufacturing teams to gain exposure to global device regulations.

The role offers hands-on regulatory experience in a multinational setting, with a focus on documentation, data verification, and regulatory updates for medical devices or combination products.

Qualifications

• Master's student in Regulatory Affairs or related field with strong regulatory interest.
• Interest in medical devices or pharmaceuticals and combination products.
• Attention to detail and willingness to learn in a cross-functional team.

Responsibilities

• Support regulatory documentation throughout the product lifecycle.
• Perform document gap assessments and verify regulatory data.
• Monitor updates to regulatory standards and assess impact.
• Update regulatory docs after product changes.
• Evaluate new regulatory requirements and change impacts.
• Prepare regulatory summaries, reports and presentations.
• Coordinate regulatory activities with project managers.
• Track actions, maintain trackers, follow up on deliverables.
• Participate in cross-functional meetings and take minutes.
• Support compliance and continuous improvement in Regulatory Affairs.
• Contribute responses to customer, authority and internal requests.
• Assist with audit preparation and corrective actions follow-up.
• Maintain regulatory databases and document management systems.
• Collaborate with cross-functional teams to ensure timely execution.

Skills

Attention to detail

Analytical skills

Organizational skills

Autonomous

Proactive

Solution-oriented

Cross-functional collaboration

Education

Master's degree student (Bac+4/Bac+5) in Regulatory Affairs

Biomedical Engineering background

Pharmaceutical Sciences background

Experience in medical devices or pharmaceuticals

Job description

Nemera, headquartered in Lyon, seeks a Regulatory Affairs Intern for a 6-month placement. Based in Lyon, you will support regulatory activities across the product lifecycle and interact with quality, design, project management, and manufacturing teams to gain exposure to global device regulations.

The role offers hands-on regulatory experience in a multinational setting, with a focus on documentation, data verification, and regulatory updates for medical devices or combination products.