Senior Manufacturing Engineer – MedTech NPI & Lean Costing

Trillium Staffing; Durham (CT); On-site; USD 120,000 - 150,000; Full time

Benefits offered by this job

Relocation assistance

Unlimited vacation/PTO

On-site with potential hybrid after 3-

Job summary

Trillium Staffing seeks a Senior Manufacturing Engineer for their Central Connecticut facility. You will lead process development, NPI, and cost-quote activities in a high-precision metals environment—ensuring manufacturability and lean improvements.

The role emphasizes ISO/FDA quality systems, CAPA, and cross-functional collaboration to impact cost, quality, and delivery. On-site initially with potential hybrid flexibility after 3–4 months.

Qualifications

• 7+ years of manufacturing engineering experience, preferably in medical device or high-precision metals.
• Strong background in metals machining, tooling/fixture design, and sub-assembly processes.
• Experience with Lean Manufacturing, problem-solving, and process optimization.
• Knowledge of ISO/FDA quality systems and GD&T principles.
• Excellent written and verbal communication with cross-functional teams and customers.

Responsibilities

• Lead process development, NPI projects, and New Product Introductions (NPI).
• Design, develop, and implement tooling, fixtures, and equipment for precision metal processes.
• Conduct root cause analysis and CAPA investigations to resolve issues and reduce waste.
• Establish standard work, process instructions, drawings, layouts, and validation protocols (IQ/OQ/PQ).
• Evaluate costing for labor, materials, and cycle times; support DFM improvements to optimize cost and quality.

Skills

Lean manufacturing

Root cause analysis

Cross-functional collaboration

Technical communication

Education

Bachelor's degree in Engineering

Job description

Trillium Staffing seeks a Senior Manufacturing Engineer for their Central Connecticut facility. You will lead process development, NPI, and cost-quote activities in a high-precision metals environment—ensuring manufacturability and lean improvements.

The role emphasizes ISO/FDA quality systems, CAPA, and cross-functional collaboration to impact cost, quality, and delivery. On-site initially with potential hybrid flexibility after 3–4 months.