Cleanroom Technology Engineer

Are you ready to drive innovation in a cutting-edge manufacturing environment? Stryker, a leading MedTech company, is seeking an experienced Manufacturing Engineer to join our team at our new manufacturing site in Skawina. We specialize in the production of titanium and stainless-steel implants and instruments, utilizing state-of-the-art processes including CNC machining, surface finishing, and cleanroom packaging. 

Join us to work in an environment where your ideas are valued, and your contributions make a real impact on patient care worldwide. Join us in shaping the future of healthcare! 

What will you do?

•  Lead significant engineering projects, including cleaning of implants and instruments 
• Provide technical leadership and operational support for manufacturing operations in our cleanroom environment. 
• Serve as a local process expert in cleaning processes
• Drive continuous improvement initiatives to enhance process performance.
• Collaborate with Process Development and Advanced Operations on technology development and application. 
• Manage the selection and qualification of machine manufacturers and suppliers. 
• Develop comprehensive work instructions, procedures, and documentation. 
• Lead the development of PFMEA, Control Plans, and process validation procedures. 
• Integrate new processes with MES/SAP systems. 
• Train and mentor operators and engineers to ensure process excellence.

What do you need?

• Master's degree in mechanics, industrial engineering, chemical engineering or similar field. 
• 4+ years of experience in serial production industries, preferably in MedTech or Automotive sectors. 
• Experience in cleanroom environments is a plus. 
• Proficiency in analytical tools such as PFMEA, SPC, MSA, and DoE. 
• Familiarity with Vision Systems, Robot programming, and advanced measuring systems. 
• Excellent PC skills and proficiency in English communication. 
• Experience in process validation and automation is highly desirable. 
• Previous experience in regulated environments based on GMP standards is advantageous. 
• Knowledge of NC/CAPA initiatives and engineering changes is a bonus.