Description
-Design and develop new methods and processes for the manufacture of new and existing products-Identify, design or purchase, and implement manufacturing aids (fixtures, jigs, tools, etc.) to reduce manufacturing costs associated with direct labor, scrap and rework.
-Perform DOE-type engineering and optimization studies
-Perform Process Validation tasks related to new products & processes (equipment qualification, PQ, PPQ)
-Selection of equipment to support manufacturing processes, including scale up of new and prototype processes
-Identify product design changes to improve quality and reduce cost
-Evaluate processes to identify areas to improve quality, cost efficiency and employee safety
-Author test protocols, reports & manufacturing documents related to new processes
-Troubleshoot product returns for root cause, identify possible solutions, and test
-Key contributor in the design and roll out of new product introduction into hi-volume production
-Apply and reinforce Design for Manufacturing (DFM) strategies to address ease of manufacturing, cost and quality goals
-Knowledge of FDA regulated medical device product manufacturing process; experience with introduction of new products, and development of new manufacturing processes.
-Thorough understanding of FDA, GSR, and cGMP requirements
To find out more about Real please visit www.realstaffing.com