Medical Devices Internship

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

Contract: 12-month fixed-term traineeship

Working arrangement: On-site position

About ProductLife Group

ProductLife Group's mission is to improve human health by delivering regulatory compliance services for the safe and effective use of healthcare solutions.

We are looking for a motivated Medical Devices Intern to join our team in Paris. This opportunity is ideal for a recent Master's graduate who wishes to develop practical experience across quality, regulatory, and clinical activities within the medical device industry.

Responsibilities

As a Medical Devices Trainee, you will support a variety of medical device activities and client projects. Your key responsibilities will include:

• Assisting with quality, regulatory, and clinical activities related to medical devices.
• Supporting compliance with applicable regulations and standards, including 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 documentation reviews, test follow-up, and data analysis.
• Collaborating with cross-functional teams to support the successful delivery of client projects.

Education and Experience

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

Technical Skills

• Knowledge of medical device regulations and standards, including EU MDR, FDA requirements, ISO 13485, and ISO 14971.
• Understanding of regulatory documentation and submission processes.
• Basic knowledge of Quality Management Systems and risk management.
• Familiarity with the medical device product lifecycle and design control.
• Ability to interpret and apply regulatory guidelines and standards.
• Strong analytical and problem-solving capabilities.

Personal Skills

• Strong communication and interpersonal skills.
• Ability to collaborate effectively with cross-functional teams and diverse stakeholders.
• Excellent attention to detail and organizational skills.
• Proactive, adaptable, and results-oriented approach.
• Ability to manage multiple priorities and meet deadlines.
• Genuine interest in medical devices, regulatory affairs, quality, and clinical activities.

Why Join PLG?

This traineeship offers the opportunity to:

• Gain hands-on exposure to medical device quality, regulatory, and clinical activities.
• Develop your understanding of international regulations and industry standards.
• Work alongside experienced professionals in a collaborative, international environment.
• Contribute to meaningful projects supporting the safety, quality, and compliance of healthcare solutions.
• Build a strong foundation for a career in the medical device and life sciences industry.

Join ProductLife Group and contribute to improving human health through safer and more effective healthcare solutions.