Test Engineer for Medical Device Development
Do you want to be part of developing safe and reliable medical devices, helping patients to better treatment? Can your expertise in mechanical and electronics testing contribute to ensure that our products are compliant with medical device regulations and standards? Do you want to cooperate with highly skilled colleagues to bring new products to market in a fast growing and successful global company?
Then you may be what we are looking for in our newly established Global Innovation & Development center in Copenhagen.
About the position:
You will be testing devices and components, develop and validate new test methods based on the product specifications to ensure that they meet requirements from users and regulatory authorities. You are experienced in translating product and regulatory requirements into testable specifications and in documenting the process and outcome.
Based on experience and statistical calculations, you will analyze the device requirements in cooperation with the project team and specify tests, test equipment and number of samples. You will deliver test reports and give the feedback to the projects regarding the statistical significance and confidence of the results. In the job you both carry out tests yourself and give guidance and support to the project engineers. Maintenance, usability and continuous improvement of tests and test methods and equipment including calibration and nonconformities reporting is also a vital part of your job.
Quality and effective execution are key words in the job, and you have great opportunities to influence the products we develop and our way of working. You will work in an international and creative environment in Copenhagen and collaborate closely with colleagues based in development and production site in Struer, Denmark.
You have a Master or bachelor’s degree in mechanical, electronical, process engineering or similar and have worked with testing in the Medical Device industry and are preferably familiar with Medical Device Regulations (21CFR, ISO13485). You are experienced with development and validation of test methods and equipment, and knowledge about applied statistics and Six Sigma is desired.
You are analytical, result oriented and a team player. You thrive by solving complex problems and understand the importance of well-structured documentation. Furthermore, you are fluent in English speaking and writing.
Are you curious to get more information?
For more information and details on the position please contact Manager, Technology and Development Lone Munk on phone +45 60387184
We look forward to hearing from you.
Please apply at your earliest convenience. We do not have an application deadline but accept applications as long as the job is posted. The position will be closed down once we have found the right candidate.
The Company – in short
Phillips-Medisize A/S is an excellent expert in the design, development and delivery of advanced drug delivery devices and connected health solutions. Our customers are leading pharmaceutical companies worldwide.
Phillips-Medisize A/S is a part of Molex. We offer innovative and integrated solutions supported by an end-to-end service offering from Strategy to Launch.
Read more about Phillips-Medisize A/S at www.phillipsmedisize.com or follow us at LinkedIn.
To apply for this job please visit phillipsmedisize.easycruit.com.