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Internship Regulatory Affairs, early development (4 – 9 months, 50 – 100 %)
Do you look for a internship to get your first working experience? Would you like to work in a young, fast-moving startup in a highly-diverse, motivated team? Would you like to get insights into Regulatory Affairs, which will direct influence the development of our products? Then contact us!
Lumendo is a young, award-winning Medtech startup, which emerged from the Swiss Federal Institutes of Technology (EPFL and ETH) and is based in Lausanne and Zürich (www.lumendo.ch). Our goal is to have an impact on society by solving clinical problems, which may arise in everyone’s life sooner or later.
Our R&D team in Zürich is responsible for the development of various injectable implants for application in dentistry, orthopedic and neurosurgery.
**As an intern**
You will support the regulatory team in their daily tasks and gradually assume responsibility for agreed individual projects. You will contribute to the regulatory affairs projects such as documentation preparation. You will support the team in writing, coordination/ collection/ storage of source documentation needed for direct submission to health authorities, and other database entry activities.
Together with our regulatory affairs and development team, you will search for and evaluate legislations, as well as guidelines from different sources and apply the gained knowledge to our ongoing development projects. You will ensure regulatory compliance by creating awareness of requirements and guidelines.
You will discover the startup environment and you will gain insights into the work of regulatory affairs and medical device development in a cross-functional, international team.
**Your tasks**
- Support of the creation and maintenance of regulatory information.
- Support of our process by preparing or updating the required documentation in order to be in compliance with the regulatory requirements.
- Coordination/ collection/ storage of source documentation.
- Search for and evaluate legislations and guidelines.
- Support the regulatory affairs and development team in defining requirements for our product.
**Your profile**
- You are a student or have graduated in the field of Sciences, Biology, Chemistry, Engineering or equivalent
- Interested in biomaterials and medical devices.
- Basic knowledge of regulations is valued, but not required. Experience in industry is a plus.
- Highly motivated and responsible; outgoing and hands-on personality.
- Independent and well-organized working style.
**What we offer**
- A work that matters and can help improve people’s life.
- A startup environment, giving you high responsibility and lots of freedom.
- A young, entrepreneurial and motivated team.
Lumendo is a young, award-winning Medtech startup, which emerged from the Swiss Federal Institutes of Technology (EPFL and ETH) and is based in Lausanne and Zürich (www.lumendo.ch). Our goal is to have an impact on society by solving clinical problems, which may arise in everyone’s life sooner or later.
Our R&D team in Zürich is responsible for the development of various injectable implants for application in dentistry, orthopedic and neurosurgery.
**As an intern**
You will support the regulatory team in their daily tasks and gradually assume responsibility for agreed individual projects. You will contribute to the regulatory affairs projects such as documentation preparation. You will support the team in writing, coordination/ collection/ storage of source documentation needed for direct submission to health authorities, and other database entry activities.
Together with our regulatory affairs and development team, you will search for and evaluate legislations, as well as guidelines from different sources and apply the gained knowledge to our ongoing development projects. You will ensure regulatory compliance by creating awareness of requirements and guidelines.
You will discover the startup environment and you will gain insights into the work of regulatory affairs and medical device development in a cross-functional, international team.
**Your tasks**
- Support of the creation and maintenance of regulatory information. - Support of our process by preparing or updating the required documentation in order to be in compliance with the regulatory requirements. - Coordination/ collection/ storage of source documentation. - Search for and evaluate legislations and guidelines. - Support the regulatory affairs and development team in defining requirements for our product.
**Your profile**
- You are a student or have graduated in the field of Sciences, Biology, Chemistry, Engineering or equivalent - Interested in biomaterials and medical devices. - Basic knowledge of regulations is valued, but not required. Experience in industry is a plus. - Highly motivated and responsible; outgoing and hands-on personality. - Independent and well-organized working style.
**What we offer**
- A work that matters and can help improve people’s life. - A startup environment, giving you high responsibility and lots of freedom. - A young, entrepreneurial and motivated team.
Not specified
Mark Bispinghoff, careers@lumendo.ch
We look forward to receiving your full application including cover letter, CV, references and transcripts of records by email. Please also state your availability.
Mark Bispinghoff, careers@lumendo.ch
We look forward to receiving your full application including cover letter, CV, references and transcripts of records by email. Please also state your availability.