Manufacturing Engineer III

Viant • Wheeling, IL

1d • $95,000 - $120,000 • Onsite

About The Position

The Manufacturing Engineer is responsible for improving manufacturing processes, supporting production operations, and ensuring products are produced safely, efficiently, and in compliance with quality and regulatory requirements. The role connects engineering, production, quality, and suppliers to drive continuous improvement and operational excellence at Viant’s precision-machining facility in Wheeling, Illinois.

Requirements

• At least 3 years of experience in the medical device industry or another regulated manufacturing environment.
• At least 2 years of experience supporting new product development and quality engineering activities.
• Experience with metal processing.
• At least 2 years of programming and hands-on machining problem-solving experience.
• Bachelor’s degree in Engineering, Quality, Manufacturing, or a related technical or scientific field, or an equivalent combination of certification and experience.
• Strong knowledge of quality engineering principles, including SPC, FMEA, DOE, process validation, root cause analysis, and CAPA methodologies.
• Proficiency in statistical analysis, Microsoft Excel, Minitab, and measurement system evaluation techniques.
• Skills in supplier quality management, qualification processes, audits, corrective actions, and continuous improvement.
• Working knowledge of Lean Manufacturing and Six Sigma methodologies.
• Strong analytical, troubleshooting, and problem-solving capabilities.
• Excellent verbal and written communication skills, including the ability to deliver training and collaborate across cross-functional teams.
• Effective project and priority management skills, with the ability to work independently in fast-paced manufacturing environments.

Nice To Haves

• CQE certification.
• Experience with FDA regulations, ISO 13485, and quality management systems.

Responsibilities

• Follow manufacturing Good Manufacturing Practices (GMPs), Viant Medical policies, and Standard Operating Procedures (SOPs).
• Manage assigned manufacturing changes and new product methods, including production fixture designs and methods for monitoring efficiency.
• Evaluate machinery and processes and recommend improvements to operator performance, ergonomics, and production safety.
• Optimize floor layout and material flow, implement lean concepts, and document improvements to manufacturing efficiency, takt time, floor-space utilization, and overhead.
• Develop or revise technical documentation specifying manufacturing processes, including equipment qualification, setup, and maintenance procedures.
• Conduct research and development testing and validation to assess manufacturing process effectiveness and compliance with quality standards.
• Confirm conformance to engineering designs and methodologies, verify overall safety, and prepare reports on these activities.
• Work with vendors to determine product specifications and arrange purchases of equipment, materials, or parts; evaluate products against specifications and quality standards.
• Use lean manufacturing analysis and troubleshooting to identify opportunities for cost, lead-time, and inventory reduction, as well as quality improvement through defect reduction.
• Perform other duties as needed.

Benefits

• Medical, dental, and vision coverage effective Day 1.
• 401(k) plan with company match.
• Paid time off and paid holidays.
• Low-cost nutrition and mental health visits.
• Tuition reimbursement and career development programs.
• Company-paid life insurance.
• Access to individualized financial planning.
• Employee discount programs.
• Home ownership program.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level