Process Engineer II - Medical Device (Onsite - Maple Grove, MN) Possible Contract Extension

Process Engineer II — Medical Device (Onsite — Maple Grove, MN) Possible Contract Extension

Be among the first 25 applicants.

Job Summary

Develop materials, processes, or equipment for projects of moderate complexity. Under limited supervision, compiles, analyzes, and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials.

Key Responsibilities

• Fully participates in and successfully contributes to project teams including product design and development, test of materials, preparation of specifications, process capability studies, report preparation, and process / test documentation.
• Works independently to plan and schedule own activities necessary to meet timelines.
• Designs and coordinates standard engineering tests and experiments.
• Designs, procures, and fabricates tooling and fixtures.
• Performs troubleshooting on new products / process problems related to material or process.
• Summarizes, analyzes, and draws conclusions from test results.
• Prepares standard reports / documentation to communicate results to technical community.
• Responsible for process engineering documentation.
• Invents / creates concepts and designs for new processes.
• May train and / or provide work direction to technicians or operators.
• Works cooperatively with R&D, quality, manufacturing, production, regulatory, and supplier management to ensure project success.
• Demonstrates PDP / TPD system knowledge through delivery of high-quality deliverables.

Quality Systems Duties

Build Quality into all aspects of work by maintaining compliance to all quality requirements.

Qualifications

Preferred Qualifications

Other Details

Metadata

J-18808-Ljbffr