We are looking for a Quality Engineer to drive excellence in supplier management, ensuring top-notch product quality. Join us to influence strategic sourcing and play a key role in our commitment to quality and regulatory standards.

What you will do:

Analyze non-conformance data to prioritize projects and address systemic supplier issues
Take ownership of Supplier-related CAPA review and management, ensuring effective use of appropriate problem-solving tools
Articulate detailed supplier performance results and trends to the appropriate levels of management
Perform PPAP activities for supplier changes
Oversee processes as a process owner and drive standardization of Supplier Quality-related processes, such as PPAP, DPM, etc.
Influence strategic sourcing, auditing, and development groups to understand the capabilities and competencies of suppliers to fulfill product quality and regulatory requirements

What You Need:

Bachelor of Science in Engineering, Mechanical Engineering, Biomedical Engineering, or related discipline
Minimum of 2 years’ experience in the field of Engineering and Quality
Experience with ISO 13485 or ISO 9001
Competence with Microsoft Office (Outlook, Excel, Word, etc.)
Good command of English
Must possess excellent oral and written communication skills
Ability to solve problems in a high-stress situation
Eagerness to assist internal and external customers
Manage projects in a timely manner with adequate priority setting and minimum supervision
Ability to conduct and document technical investigations

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

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Quality Engineer in Kayseri, Turkey