Product Development Engineer - Medical Devices
At Elos Medtech we give you the chance to grow. To shape your own career. To work in an international environment. To be part of a company that supports the global implant market. We offer you a world of opportunities – if you have the ability and the drive to take them.
Elos Medtech is looking for a highly motivated and skilled Product Development Engineer for mechanical engineering who would like to work with international development projects and contribute to the development of Elos Medtech’s dental product portfolio.
Product Development - your new team
You will be a part of the Product Development department based at Elos Medtech in Denmark as part of the Dental Business Unit, Product innovation, and life cycle management.
Our team develops and registers Elos Medtech’s products for the dental industry and makes sure that all technical documentation complies with medical device regulations. Additionally, we help our customers with the design for manufacturing, sourcing, materials, new packaging/labeling, and manufacturing processes.
Empowerment, trust, and a high level of personal commitment characterize our work environment.
Your main responsibilities
- Be part of multidisciplinary medical device development projects and customer projects.
- Mechanical design, setting tolerances, material selection, defining manufacturing processes, and design for manufacturing.
- Verification testing and design validation.
- Establishment of technical documentation (design control) in compliance with our development process and international medical device regulations (ISO 13485 and FDA etc.).
- Optimize and implement changes to Elos Medtech’s own dental products.
Short periods of travel activities in relation to customer projects are expected.
We work in cross-functional teams and you will work in collaboration with production engineering, product management, the commercial department, and our regulatory affairs team. As the project activities in the department are highly characterized by delegation, you must be ready to take responsibility. In your daily work, you will report to our Manager of Product Development & Regulatory Affairs.
Your qualifications
- You have an educational background as B.Sc or M.Sc. in mechanical engineering.
- You preferably have 3-5 years of experience with product development or manufacturing processes within the medical device industry.
- You are experienced and comfortable or willing to learn to create Design Control documentation according to ISO 13485 and FDA (21 CFR Part 820).
- You are experienced in 3D CAD modeling, preferably PTC Creo.
- You are driven by results, and you can manage your own tasks plus work on multiple projects simultaneously.
- You are fluent in Danish and have a high level in English, written and spoken.
As a person, you are a motivated team player, open-minded, and proactive with a can-do attitude to your work.
Contact
Please apply as soon as possible. Applications are accepted in English and Danish. We will review applications and hold interviews on an ongoing basis until the position is filled.
For further information about the position, feel free to contact Søren Rangstrup, Manager of Product Development & Regulatory Affairs: soren.rangstrup@elosmedtech.com / +45 20 66 64 42.
We look forward to receiving your application!
