Manufacturing Engineer (12 months contract)

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.