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Sr. Manufacturing Engineer for MDR validation project H/F – Dispositifs médicaux -Paris

You will work at a large American group. A good command of English is indeed mandatory for this position.

Job Responabilities : 

– Interface with R&D, quality engeneering, purchasing, logistics, production, regulatory, and external vendors to resolve manufacturing related issues. 

– Develop manufacturing processes by understanding product requirements : researching, designing, and testing manufacturing methods and equipment to enhance productivity and product quality. 

– Improve manufacturing process capability and establish process control specifications. 

– Create process validation master plan. Create equipment specification and software requirements.

– Participate new product development phase reviews and provide inputs representing manufacturing operations. 

– Create or update production documentations and train production personnel and technicians on processes. 

– Analyze and improve manufacturing process capability and product quality. 

You hold a Master’s degree in mechanics, biomedical, or related discipline, and have a minimum of 5 years of experience in the medical industry.

Knowledge and Skills : 

– Knowledge and experience in Lean Manufacturing. 

– Mechanical drawing reading and engineering level mathematics. 

– Working knowledge of CAD and Minitab.

– Strong analytical and problem-solving skills. 

– Ability to define, write, and perform test protocols for manufacturing process development. 

– Ability to create detailed tooling and fixture drawing.

– Ability to create a basic strategy for new product process and equipment development and qualification. Set priority, plan, execute, and implement project from concept to completion independently.