Participates in project teams typically including one of the following: identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance; designing, performing, and documenting engineering test experiments to evaluate product/product performance; participating in Quality improvement activities; designing, developing, testing, and validating equipment, tools and fixtures; analyzing and interpreting process models and recommending process improvements; evaluates external process technologies; and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific narrow area of assignments. Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification. Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification. Has working knowledge of Risk Management & Failure mode and effect analysis (FMEA) requirements. Interfaces with assemblers, production supervisors, and engineers in troubleshooting problems on the production floor. Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans. Acts independently to implement and follow through. Perform root cause analysis of failed product. Participates in project planning and scheduling. Optimize processes for yield improvements, cycle time improvements, and scrap reduction. Attends and contributes to product core team meetings. Performs responsibilities required by the Quality System and other duties as assigned or requested. Bachelor's degree in mechanical, Electromechanical, Electronic, Biomedical, Chemistry, Industrial, Electrical, Industrial Maintenance or Equivalent experience. English Level desired: 80-89%. Desired knowledge: Process Manufacturing Certification, Problem Solving, Regulatory industry management, Regulatory Affair, Networking, Process Validations, Stadistical and Experimental Analysis, DOE, Solid Works, Transfer Process, MiniTab, Hands & Statisctics, Validation Process, Tools (Statistics, Technical Manuals, Kaizen, Six Sigma), Regulatory industry management. At least 3 years of experience in similar position. Or an equivalent combination of education and experience. Requisition ID: 621729 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! Benefits Life-Work Integration Community * Career Growth With determination, imagination, and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life's work. CRTA #CTGTA