Manufacturing Engineer
hace 4 semanas
What you will do-
Job Summary
Support Manufacturing/Operations in the following areas: increase capacity, reduce scrap, improve safety, monitor existing processes, identify and implement process improvements in a regulated medical device reprocessing environment.
Responsibilities and Functions
- Support and improve existing processes using Statistical, Lean, Good Manufacturing Practice (GMP) and Six Sigma methodologies.
- Effectively transfer new products, design changes or line extended devices onto the production floor. Foster an environment of continuous improvement and provide support to customers in all functional areas.
- Discuss progress and interim findings at periodic design/project review meetings. Perform Failure Analyses (FAs) and improve Functionality/Performance of medical devices. Implement process improvements and machining improvements on production lines.
- Reduce Reject Rates (scrap) and optimize manufacturing processes. Implement safety improvements on production lines. Assist in the development and execution of technical protocols and generation of reports.
- Implement operating procedures, standard work, visual work instructions, and visual work references.
- Assist with training to Production for all new product launches and design changes to existing products or processes.
- Expectation of acquired knowledge of FDA/ISO requirements associated with the development of medical devices including Design Control.
- Perform other duties as directed or assigned by Manager.
What you need-
- B.S. engineering (Industrial, Mechanical, or Electrical).
- Bilingual: English & Spanish.
- No previous experience required.
- Internship experience preferred.
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