Project Engineer II - Medical Device Capital & Process Lead

Integra LifeSciences Corporation; Tennessee; On-site; USD 62,000 - 85,000; Full time

Job summary

Integra LifeSciences Corporation in Cordova, TN is seeking a Project Engineer II to coordinate with production, quality, R&D and suppliers to manage capital projects and continuous improvements, ensuring on-time delivery within budget.

The role emphasizes leading design transfer, process validation (IQ/OQ/PQ), root-cause investigations, and mentoring junior engineers, with 5–10% travel and strong cGMP knowledge.

Qualifications

• Bachelor’s degree in Chemical or Mechanical Engineering.
• Minimum 3 years of industry experience in engineering; medical device experience preferred.
• Lean Six Sigma experience is a plus.
• Cleanroom manufacturing experience is a plus.

Responsibilities

• Provide project management for capital projects, continuous improvement projects, design transfer projects, and system projects (SCADA, CMMS, etc.).
• Lead continuous improvement programs by implementing measures to improve production methods, equipment performance, and quality of product.
• Evaluate, implement, and monitor processes and equipment for the manufacture of medical products.
• Function as the manufacturing lead for process validation and process monitoring.
• Author & review IQ, OQ, and PQ protocols in addition to validations.
• Provide key technical and project management support in capital projects.
• Interface with procurement to identify and evaluate new and replacement raw materials.
• Mentor junior engineers on cGMPs and good engineering practices.
• Travel 5% – 10% as required.

Skills

Project management

Root cause analysis

Cross-functional collaboration

cGMP knowledge

Data analysis

Education

Bachelor’s degree in Chemical Engineering or Mechanical Engineering

Tools

CAD (SolidWorks)

Minitab

SCADA

CMMS

Job description

Integra LifeSciences Corporation in Cordova, TN is seeking a Project Engineer II to coordinate with production, quality, R&D and suppliers to manage capital projects and continuous improvements, ensuring on-time delivery within budget.

The role emphasizes leading design transfer, process validation (IQ/OQ/PQ), root-cause investigations, and mentoring junior engineers, with 5–10% travel and strong cGMP knowledge.