Manufacturing Engineer (12 Months Contract)

Work Flexibility: Onsite

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

1. Support and improve existing processes using Statistical, Lean, Good Manufacturing Practice (GMP) and Six Sigma methodologies.
2. 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.
3.
Discuss progress and interim findings at periodic design/project review meetings.
4. Perform Failure Analyses (FAs) and improve Functionality/Performance of medical devices.
5. Implement process improvements and machining improvements on production lines.
6. Reduce Reject Rates (scrap) and optimize manufacturing processes.
7. Implement safety improvements on production lines.
8. Assist in the development and execution of technical protocols and generation of reports.
9. Implement operating procedures, standard work, visual work instructions, and visual work references.
10. Assist with training to Production for all new product launches and design changes to existing products or processes.
11. Expectation of acquired knowledge of FDA/ISO requirements associated with the development of medical devices including Design Control.
12. Perform other duties as directed or assigned by Manager.

What you need

1.
B.S. engineering (Industrial, Mechanical, or Electrical).
2. Bilingual: English & Spanish.
3. No previous experience required.
4. Internship experience preferred.

Travel Percentage: 10%

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