NPI Process Engineer: Manufacturing Excellence & Scale-Up

EXALTA Group's; Athens (AL); On-site; USD 85,000 - 110,000; Full time

Job summary

EXALTA Group's is seeking an NPI Process Engineer to lead technical decisions for new product introductions, ensuring manufacturability and scalability. You will guide process design, materials selection, and production readiness to meet specifications and quality goals.

You will collaborate with design and QA teams, oversee prototypes, and develop robust documentation, with emphasis on DFMA input and continuous improvement in a regulated medical device setting.

Qualifications

• Bachelor’s degree in Engineering or related field or equivalent experience.
• Minimum 3 years in ISO/FDA machine shop or contract manufacturing.
• Experience in a medical device, ISO/FDA, job shop environment preferred.

Responsibilities

• Develop and optimize manufacturing processes for new products.
• Provide input on design for manufacturability (DFM) and design for assembly (DFA).
• Oversee prototypes and pilot runs and adjust before full-scale production.
• Create and maintain manufacturing documentation and work instructions.
• Implement quality control measures and inspections to ensure standards.
• Collaborate with production planners to develop schedules and capacity plans.
• Identify opportunities to reduce production costs without compromising quality.
• Train staff on new processes and equipment.

Skills

GD&T interpretation

Adaptability

Mathematics

Critical thinking

Team collaboration

Communication

5S practices

Flexible hours

Documentation

Education

Bachelor's degree in Engineering or related field

Technical degree or equivalent

Tools

CAD Autodesk Inventor

Microsoft Outlook

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Job description

EXALTA Group's is seeking an NPI Process Engineer to lead technical decisions for new product introductions, ensuring manufacturability and scalability. You will guide process design, materials selection, and production readiness to meet specifications and quality goals.

You will collaborate with design and QA teams, oversee prototypes, and develop robust documentation, with emphasis on DFMA input and continuous improvement in a regulated medical device setting.