Intern RDI Academy Product Development

at  Straumann Group

Headquartered in Basel, Switzerland, Straumann is a global leader in implant and restorative dentistry and oral tissue regeneration. Having pioneered many of the most influential technologies and techniques in our field, we have a tradition of doing more to advance dental regeneration, restoration and replacement, as well as patient care. Straumann is renowned for providing profound clinical evidence to support the product portfolio and bring new solutions to the market.
We are looking for an intern to join our Life Cycle Management (LCM) team for a period of 6 months. The ideal candidate will have a level of familiarity and strong interest in dental implants and prosthetics, medical device regulations, applicable standards, and root cause analysis. The internship offers the opportunity to get real-life experience with life cycle management for products within the medical device/dental field.

EDUCATION:

• Bachelor’s or Master’s degree in life sciences, mechanical engineering, material science or equivalent field

REQUIREMENTS:

• Familiarity with medical devices, quality management system, manufacturing processes and applicable regulations
• Ability to work on documentation, that follows good documentation practices
• Good organization skills
• Proficiency in English (spoken and written)
• Familiarity with MS Office (Word, Excel, Project, etc.)

• Assist the LCM team in daily operations by actively participating in project activities, including the review and organization of technical documents and relevant supporting materials.
• Collaborate with cross-functional teams to contribute to the execution and monitoring of LCM activities, helping to identify and resolve product-related issues.
• Provide support for lifecycle management (LCM) projects focused on dental implants, prosthetic components, and surgical instruments, ensuring products adhere to regulatory, quality, and functional requirements.
• Assist in the preparation, maintenance, and organization of documentation needed for LCM projects, ensuring compliance with internal standards and regulatory guidelines.
• Support with administrative tasks related to activities of product LCM