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Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
As a Senior Quality Engineer (m/f/d) at Stryker, you'll play a pivotal role in driving quality and excellence in our products, including fixation systems. You will design and implement cutting-edge methods for process control, improvement, testing, and inspection, ensuring our products meet the highest standards of performance and reliability.
Join us and be part of a team that’s shaping the future of healthcare, delivering innovative solutions that improve lives worldwide.
What you will do
Design, implement, validate, and optimize advanced testing systems, conducting detailed product analyses to maintain consistent quality and minimize defects and failure rates.
Evaluate quality reports and defective product data to identify trends, root causes, and actionable solutions for improvement.
Collaborate closely with suppliers to address quality challenges, ensure the implementation of effective corrective actions, and actively contribute to supplier quality improvement initiatives.
Participate in internal and external audits, including audit preparation and logistics, and provide expertise during audits as needed.
Manage and approve product releases, QM documents, change management (ECR/ECN), and local product blocks and releases.
What you will need:
Required:
Bachelor’s or Master’s degree in Science, Engineering, or a related field, or equivalent technical qualifications.
2–6 years of professional experience in a quality-related role, such as supplier quality management, change management, or NC/CAPA processes.
Strong mechanical background and a deep understanding of manufacturing processes, including experience in PFMEA or PPAP.
Excellent English and German language skills, enabling seamless collaboration with global stakeholders.
Preferred:
Previous experience in the medical device or manufacturing industry.
Diversity is important to us. We welcome applications from people regardless of their ethnic, national or social origin, gender, disability, age or sexual identity.
Additional information
Please note that the internal job title may differ from the ad title.