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Senior / Staff Quality Engineer (m/f/d) NPI New Product Introduction
vor 4 Monaten
Why engineering at Stryker?
At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development.
Need another reason to apply? Check out these 8 reasons to join Stryker's engineering team:
As a Senior / Staff Quality Engineer (m/f/d) NPI New Product Introduction at Stryker you will have an incredible opportunity to support the introduction of new, innovative medical devices and help improving the lives of patients around the globe. Feel free to check out OptaBlateTM, where you can find some of the devices that the department worked recently on.
Your key responsibilities
As a Senior / Staff Quality Engineer (m/f/d) NPI you will execute design for manufacture and assembly through technical understanding of quality assurance, design control and preventative activities.
You will support the development and introduction of new products, processes, and technologies, with focus on risk management
You will provide quality engineering support for the execution of quality assurance activities during design transfer phases of new product development.
You will provide Quality engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.
Etc.
What are we looking for?
You have completed B.S in Engineering or related subject.
You have a minimum of 2 years’ experience in a regulated environment within a manufacturing environment (Medical Device is an advantage). Depending on your experience, the level of seniority may vary.
Ideally you are familiar with Qualification & Validation in regulated environment OR you are knowledgeable in CSV (Computer System Validation).
You bring over 2 years of experience in quality assurance or process management within a manufacturing or production environment.
You have good problem solving and communication skills, as well as attention to detail.
Your excellent English and German language skills enable you to collaborate with stakeholders on a global basis.
Additional information
Thanks to our flexible working hours model, you will have the opportunity to work partially from the home office. However, a regular presence of 2/3 days a week on site at our location in Freiburg should be always given to build sustainable relationships and maintain personal contact with colleagues as well as the departments.
Your application
We are looking forward to your online application including all relevant documents such as CV in English, cover letter, transcript of results, and references. Please note to upload all attachments directly in our application procedure under the item "CV".
Please note that the internal job title may differ from the ad title.
Your contact:
In case you have further questions regarding the position, please feel free to directly reach out to Monika Ambroziak: @
About StrykerStryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 130 million patients annually. More information is available at
