Medical Devices Trainee - Regulatory, Quality & Clinical

ProductLife Group; Paris; Sur place; EUR 12 000 - 19 000; Plein temps

Résumé du poste

ProductLife Group in Paris is seeking a Medical Devices Intern to join the team for a 12-month fixed-term traineeship on-site in Paris. This role is ideal for a recent Master's graduate seeking hands-on experience across quality, regulatory, and clinical activities in the medical device industry.

You will support diverse activities, including quality, regulatory submissions, technical documentation, and vigilance.

Qualifications

• Master's degree in a relevant scientific, engineering, quality, regulatory, biomedical, or life sciences discipline.
• Recent graduates and junior candidates are welcome to apply.
• Academic background or initial exposure to medical devices would be advantageous.
• Fluency in both French and English is required.

Responsabilités

• Assisting with quality, regulatory, and clinical activities related to medical devices.
• Supporting compliance with EU MDR, IVDR, FDA requirements, and ISO 13485.
• Contributing to the preparation and maintenance of technical documentation.
• Supporting regulatory submissions and clinical evaluation documentation.
• Assisting with promotional material reviews.
• Supporting complaint handling and vigilance activities.
• Contributing to verification and validation activities, including reviews, test follow-up, and data analysis.
• Collaborating with cross-functional teams to support client projects.

Connaissances

EU MDR

FDA requirements

ISO 13485

ISO 14971

Regulatory docs

Formation

Master's degree (life sciences)

Description du poste

ProductLife Group in Paris is seeking a Medical Devices Intern to join the team for a 12-month fixed-term traineeship on-site in Paris. This role is ideal for a recent Master's graduate seeking hands-on experience across quality, regulatory, and clinical activities in the medical device industry.

You will support diverse activities, including quality, regulatory submissions, technical documentation, and vigilance.