Stryker
Location
Tuttlingen | Germany
Job description
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 Quality Engineer (m/f/d) at Stryker in Tuttlingen, you will play a crucial role in ensuring the highest standards of quality within o ur Communications Business . Your impact will extend beyond ensuring compliance – you'll be at the forefront of pioneering quality advancements, driving innovation, and shaping the future of cutting-edge medical technology.
Join a dynamic team that values your contributions and fosters a culture of continuous growth and development.
What will you do
As a Senior Quality Engineer (m/f/d) at Stryker, you will provide quality engineering support and direction in quality assurance, control and preventative activities within operations with a focus on preventative measures and continuous improvement of products and processes.
You will advocate and lead the execution of initiatives & projects to enhance quality performance within the business.
You will work closely with operations, suppliers and the business functions to ensure a high-quality supply chain with quality performance of product and processes.
You will take the lead in oversighting, performing and approving NC & CAPA.
You will take an active role in resolving issues, contributing to problem-solving and root cause analysis activities.
You will lead and participate in the development and improvement of the manufacturing processes for existing and new products.
What will you need
You have completed BS in medical technology, industrial engineering, mechanical engineering or related degree.
You have gained a minimum of 2 years’ experience in medical technology or another regulated sector in the area of quality.
You are familiar with common project management methods and quality techniques (e.g. p-FMEA, NC/CAPA, RM, Risk Assessment, Risk Evaluation) and have gained experience in applying these methods.
Ideally, you have knowledge of regulatory requirements and manufacturing guidelines for medical devices, including FDA guidelines, GMP and DIN ISO 13485.
Your English and German language skills enable you to collaborate with colleagues and stakeholders on a global basis as well in the local office.
Your application
We are looking forward to your online application including all relevant documents such as CV, 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: [email protected]
Job tags
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