Senior Product Test Engineer (m,f,d) - Medical Devices

Your Job

Do you want to design safe and reliable medical devices, bringing our clients' life-changing solutions into the hands of patients and helping patients to get better treatment? Then you may be the Senior Product Test Engineer we are looking for in the Phillips-Medisize Global Innovation & Development Center (Virum or Struer) where you will work together with highly skilled colleagues to bring new products to market in a fast-growing and successful global company!

As a Senior Product Test Engineer you will be an essential contributor in the development and designing optimal verification methods for requirement confirmation.

You will have the responsibility to ensure timely delivery of test results according to project schedule with patient safety in focus.

Further you will be an essential contributor for coordinating of interdisciplinary product test related activities.

Our Team

You will be part of the product test team which is currently based in both Virum and Struer.

As Senior expired product test engineer also contributing to the development of the team and optimization of processes and methods.

What You Will Do



* Responsible for testing products and components in compliance with applicable specifications


* Development of tests, measurements, and processes to achieve the most efficient and effective coverage of all components and requirements


* Coordination of interdisciplinary product test related activities within assigned projects


* Systematization, analysis and documentation of test data


* Work and document using agreed methods and tools including QMS, calculations, simulations, measurements, test results etc.


* Develop and provide appropriate and accurate information to partners within and outside Phillips-Medisize in terms of documentation, design review etc.

Who You Are (Basic Qualifications)


* Degree in Mechatronics Engineering, Electrical Engineering, Mechanical Engineering or similar qualification


* Proven experience (minimum 5 years) with complex medical devices product testing


* Systematic and direct


* Strong technical understanding and the ability to read, analyze and interpret technical procedures and governmental regulations


* Independent and conscientious way of working


* Ability to work in teams, reliable and flexible


* Fluent in English


* Knowledge of MS Office, Access and other relevant IT tools or systems

What Will Put You Ahead



* Experience within medical device industry and familiar with regulations and standards (e.g., 21 CFR 210/211/820, ISO 14971, ISO 13485, ISO 11608) preferred.


* Experience with statistics.


* Experience in system and risk management engineering as well as design control, change control and deviation handling .


* Knowledge of SAP.

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