Life Sciences Internship at ProductLife Group, France | Medical Devices Traineeship
How do medical device teams bring together quality, regulatory compliance, and clinical evidence? This Life Sciences internship at ProductLife Group offers recent master’s graduates practical exposure to these activities through medical device projects. Based in the Paris area, France, the 12-month traineeship involves technical documentation, regulatory submissions, and collaboration with experienced professionals.
- Position: Medical Device Internship
- Location: Courbevoie Office / Paris, Île-de-France, France
- Job Requisition ID: JR000071
- Employment Type: Full-time traineeship
About The Company
ProductLife Group provides regulatory compliance services supporting the safe and effective use of healthcare solutions. Its mission is to improve human health through expertise and collaboration across the life sciences industry.
Life Sciences Internship Description
The Medical Devices Trainee will support quality, regulatory, and clinical activities across medical device projects. The role includes preparing documentation, supporting compliance with international requirements, and contributing to client project delivery.
The opportunity is intended for recent master’s graduates and junior candidates interested in building practical experience in medical devices, regulatory affairs, and quality.
Key Responsibilities
- Assist with quality, regulatory, and clinical activities related to medical devices.
- Support compliance with EU MDR, IVDR, FDA requirements, and ISO 13485.
- Help prepare and maintain technical documentation.
- Support regulatory submissions and clinical evaluation documentation.
- Assist with promotional material reviews.
- Support complaint handling and vigilance activities.
- Contribute to verification and validation through documentation reviews, test follow-up, and data analysis.
- Collaborate with cross-functional teams on client projects.
Educational Requirements and Eligibility
- Qualification: Master’s degree in a relevant scientific, engineering, quality, regulatory, biomedical, or life sciences discipline.
- Experience: Recent graduates and junior candidates are welcome.
- Languages: Fluency in both French and English is required.
- An academic background or initial exposure to medical devices is advantageous.
Skills and Qualifications For Life Sciences Internship
- 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 lifecycle and design control.
- Ability to interpret and apply regulatory guidelines.
- Strong analytical, problem-solving, communication, and teamwork skills.
- Attention to detail, organization, and ability to manage competing priorities.
- A proactive approach and interest in medical device quality, regulatory, and clinical work.
Training and Development
The traineeship offers hands-on exposure to international medical device regulations and industry standards, alongside experienced professionals. Participants will contribute to projects supporting healthcare product safety, quality, and compliance.
Application Details For Life Sciences Internship
- Application Deadline: December 30, 2026.
- Contract Duration: 12-month fixed-term traineeship.
- Expected Start Date: The description lists September 2026; confirm the current start date with the employer.
- Working Arrangement: The listing header says hybrid, while the detailed description specifies onsite work. Confirm before applying.
Interested in understanding what keeps medical devices safe and compliant throughout their lifecycle? This Life Sciences internship at ProductLife Group combines regulatory documentation, quality activities, and clinical project support. If you hold a relevant master’s degree and are fluent in French and English, review the opportunity and submit your application.
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