Actively shape the process development and ensuring that all activities are completed and documented in accordance with the Stryker procedures.
Responsible for solving technical challenges and implementing efficient manufacturing and testing strategies in a highly technical environment.
Make a significant contribution to the realization of short transfer times, considering innovative problem-solving methods, continuous development and optimization of our manufacturing processes.
Work closely with cross functional teams and international project teams and process experts.
Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers.
Complete capability and MSA studies for in process inspection and generate subsequent Inspection documentation.
What you will need:
Required Qualifications:
Engineering degree (automation technology, process engineering, electrical engineering, mechanical engineering, medical technology, industrial engineering or similar)
4 to 8 years of professional experience in the field of process development and/or process optimization.
Strong knowledge of Quality Concepts and Risk Based Techniques (e.g. FMEA, Risk, Statistics).
Have a good understanding of engineering, validation cycle and machine tool fundamentals.
Good knowledge of manufacturing processes, materials, product and process design.
Must be able to read and interpret complex engineering drawings and can understand geometrical dimensioning and tolerancing.
Preferred Qualifications:
Excellent Interpersonal Skills
Excellent analytical skills, ability to plan, organize and implement concurrent tasks
Individual is willing to travel occasionally for business purposes
