R&D Engineer - Class 3 Medical Devices

R&D Engineer - Class 3 Medical Devices

Cook Medical

Bjæverskov, Denmark

We are looking for an Engineer who is passionate about technical design, technology, and is highly motivated by developing new Class 3 products for the treatment of patients with vascular diseases. Have you got a distinctly good overview, do you do well in high complexity, and do you also thrive on succeeding in something difficult? – then you are exactly the person we need.

The right person:

• is self-driven and has a can do and will do attitude.
• thrives in being part of a large team and global organization.
• is patient when it comes to ensuring details and high quality of work.
• is result oriented and understands the broader perspective.
• can balance humor and professionalism in a good way.
• has an empathetic and inclusive approach.

Responsibilities:

Job profile:

We are looking for a skilled Engineer, preferably with knowledge from the medical industry, who wants to be part of an international Research & Development environment, where we develop innovative solutions enhancing people’s quality of life all over the world. You will be part of a large and skilled development team, where there is a lot of room for the individual.

As an Engineer in the Aortic Intervention department, you contribute to the development and maturation of the product in all its development phases.

The job requires both technical insight and ingenuity as well as the ability to structure large amounts of information and documentation. We work in interdisciplinary projects where traditional engineering disciplines are combined with both physiological and clinical understanding. It all happens in a close cooperation with colleagues in Denmark, the U.S. and Australia, respectively.

You will be part of all the development phases of the project, from idea to finished product as well as:

• collect requirements for new products and translate these into product concepts.
• design and test of prototypes
• prepare product documentation including, e.g., Design Input Requirements (DIR), test plans, risk analysis and usability documentation.
• ensure completion of design verification tests and generate relevant statistical analysis.
• validate test methods in cooperation with colleagues in the R&D Process Development department.
• collect requirements for new products and translate these into product concepts.

Qualifications:

We expect that you:

• are an engineer, e.g., in medicine/technology, design/innovation, mechanics, biomedicine or similar.
• preferably with experience from product development and preparation of documentation for use in global regulatory approvals
• are fluent in verbal and written English (corporate language)

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