Work Flexibility: Hybrid
What you will do:
- 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
Travel Percentage: 20%