Engineer, Sr Mfg - 100146 - San Jose,CA - 0300

Biotechnology and Pharmaceutical Engineer, Sr Mfg - 100146 - San Jose,CA - 0300 Job Description:Responsibilities:The Senior Manufacturing Engineer will have responsibility for the planning and execution of process engineering projects, interfacing with suppliers and Machine Shop. Projects are defined as product improvement/expansion programs, cost reduction programs, procurement of machinery, validation of new equipment and materials, capital projects and facilities expansion projects. Specific Duties and Responsibilities: Develop process parameters for new equipment. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification (IQ,OQ,PQ). Release process documentation for new processes and train production on processes. Optimize processes for yield improvements, cycle time improvements, and scrap reduction. Implement Lean manufacturing concepts to eliminate non-value added activities. Perform root cause analysis of failed product. Participate in product development project to ensure that the project team is designing for manufacturability (DFM) in the development phases of the project. Coordinate design transfer on new products into manufacturing. Perform any other duties assigned by Manager.Position Qualifications:BS degree required in Mechanical, Electrical, Chemical, Manufacturing, or Materials Engineering. 3 to 8 years related experience or equivalent combination of education and experience. 3 years experience should be with a medical device manufacturer in a GMP and ISO environment; or equivalent combination of education and experience to perform at this level. Six Sigma is a plus!Job Experience:Responsibilities:The Senior Manufacturing Engineer will have responsibility for the planning and execution of process engineering projects, interfacing with suppliers and Machine Shop. Projects are defined as product improvement/expansion programs, cost reduction programs, procurement of machinery, validation of new equipment and materials, capital projects and facilities expansion projects. Specific Duties and Responsibilities:• Develop process parameters for new equipment. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification (IQ,OQ,PQ).• Release process documentation for new processes and train production on processes.• Optimize processes for yield improvements, cycle time improvements, and scrap reduction.• Implement Lean manufacturing concepts to eliminate non-value added activities.• Perform root cause analysis of failed product.• Participate in product development project to ensure that the project team is designing for manufacturability (DFM) in the development phases of the project. Coordinate design transfer on new products into manufacturing.• Perform any other duties assigned by Manager.Position Qualifications:BS degree required in Mechanical, Electrical, Chemical, Manufacturing, or Materials Engineering. 3 to 8 years related experience or equivalent combination of education and experience. 3 years experience should be with a medical device manufacturer in a GMP and ISO environment; or equivalent combination of education and experience to perform at this level. Six Sigma is a plus!Minimum Education Required: BachelorYears of Experience Required: More than 5 yearsExpected Travel Time: None Please visit us online at www.bostonscientific.com for more information.