- Actively shape the process development and ensuring that all activities are completed and documented in accordance with the Stryker procedures.
- Coordinate with internal and external partners, 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 will you need
Basic Qualifications:
- Master's or bachelor's degree in engineering (automation technology, process engineering, electrical engineering, mechanical engineering, medical technology, industrial engineering or similar) with 5 to 8 years of professional experience in the field of process development and/or process optimization.
- Hands on experience with Medical Device Post Market Surveillance.
- Experience with Product development/ Transfer, Process Engineering, Supplier development /PPAP.
- Good knowledge of manufacturing processes, materials, product and process design.
- Able to read and interpret complex engineering drawings and has the ability to understand geometrical dimensioning and tolerancing.
Preferred Qualifications:
- Excellent Interpersonal and analytical Skills.
- Individual is willing to travel occasionally for business purposes
- Experience in an FDA regulated or regulated industry beneficial