Engineer II, Mfg - 100147 - Fremont, CA - 0300

Biotechnology and Pharmaceutical Engineer II, Mfg - 100147 - Fremont, CA - 0300 Job Description:Responsibilities: The manufacturing engineer will, as assigned by a project team/supervisor/senior engineer, independently perform any of the following: Plans, schedules, conducts and coordinates detailed phases of engineering work as part of a PDP project or as a total project of moderate scope. Develops specifications of a product, process or piece of equipment. Performs equipment qualifications. Develops, characterizes and optimizes processes using statistical techniques, engineering knowledge, and experience. Performs process validations. Performs production support activities. Monitors process and equipment performance. Identifies and implements process improvement activities to increase/optimize yield, efficiency or throughput. Creates and maintains production documentation and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific area of assignments. Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process improvement plans. Participates in project planning and scheduling. Trains assemblers, quality control and technicians, as necessary, on processes, equipment and documentation. Qualifications: Minimum education: B.S. in Mechanical, Electrical, Chemical, Materials, Plastics or Industrial Engineering or related degree with 2 years related experience, or MS with a minimum of 1 year experience, a minimum of 2 years prior Engineering standing. Engineering experience in a manufacturing environment recommended, medical device industry preferred. Knowledge of FDA regulations preferred. Knowledge of JIT and/or Lean/Flow Manufacturing helpful. Knowledge of materials and manufacturing processes helpful. Six Sigma experience a big plus!Job Experience:Responsibilities: The manufacturing engineer will, as assigned by a project team/supervisor/senior engineer, independently perform any of the following: • Plans, schedules, conducts and coordinates detailed phases of engineering work as part of a PDP project or as a total project of moderate scope. • Develops specifications of a product, process or piece of equipment. • Performs equipment qualifications. • Develops, characterizes and optimizes processes using statistical techniques, engineering knowledge, and experience. • Performs process validations. • Performs production support activities. Monitors process and equipment performance. • Identifies and implements process improvement activities to increase/optimize yield, efficiency or throughput. • Creates and maintains production documentation and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific area of assignments. • Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process improvement plans. • Participates in project planning and scheduling. • Trains assemblers, quality control and technicians, as necessary, on processes, equipment and documentation. Qualifications: Minimum education: B.S. in Mechanical, Electrical, Chemical, Materials, Plastics or Industrial Engineering or related degree with 2 years related experience, or MS with a minimum of 1 year experience, a minimum of 2 years prior Engineering standing. Engineering experience in a manufacturing environment recommended, medical device industry preferred. Knowledge of FDA regulations preferred. Knowledge of JIT and/or Lean/Flow Manufacturing helpful. Knowledge of materials and manufacturing processes helpful. Six Sigma experience a big plus!Minimum Education Required: BachelorYears of Experience Required: At Least 3 YearsExpected Travel Time: None Please visit us online at www.bostonscientific.com for more information.