Work Flexibility: Hybrid

What will you doActively 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 purposesExperience in an FDA regulated or regulated industry beneficial

Travel Percentage: 10%