Description
Responsibilities:
The Manufacturing Engineer II will independently evaluate, select, and apply standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications in a medical device clean room environment. Assignments have clear and specified objectives and require the investigation of a limited number of variables. Improve existing manufacturing processes and act as liaison between production and engineering group in resolving problems encountered on the production floor.
Specific Responsibilities:
Provide mechanical engineering input to help in tooling design and fixturing. Release process documentation for new processes and train production personnel on processes. Interface with assemblers, production supervisors, and engineers in troubleshooting problems on the production floor. Coordinate with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans. Engage in Lean and Six Sigma activities ensuring manufacturing efficiency by cost, quality, yield, scrap, and throughput analysis. Other duties as assigned by manager.
Requirements:
BSME required. A minimum of two years related experience preferable with a medical device manufacturer in a GMP and ISO environment. Experience in manufacturing environment. Strong technical and organization skills. Excellent verbal communication skills. Knowledge of Good Manufacturing Practices (GMP). Knowledge of JIT a plus. Knowledge of materials and manufacturing processes helpful. Or, equivalent combination of education and experience to perform at this level.
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