Manufacturing Process Engineer - Medical Device (12 hour rotational shift)

Micro Stamping Corporation•Franklin Township, NJ

66d•Onsite

About The Position

The Process Engineer ensures manufacturing processes are efficient, cost-effective, compliant with MICRO’s quality standards, and capable of consistently producing products that meet customer specifications.

Requirements

Bachelor’s degree in Engineering or a related field is required.
At least 4-6 years of engineering experience is required.
Blueprint reading
Geometric Dimensioning and Tolerancing (GD&T)
Statistical Process Control (SPC)
Measurement Systems Analysis (MSA, GR&R)
Design of Experiments (DOE)
Statistical software systems
ERP
Minitab Statistical Software
Metal fabrication
Medical device manufacturing
MS Office Suite
Verbal communication
Written communication
Organizational skills
Problem solving

Responsibilities

Lead projects that deliver measurable improvements in process efficiency, product quality, and cost reduction across assigned manufacturing areas.
Act as a Subject Matter Expert (SME) to resolve complex technical challenges, optimize process performance, and support cross-functional teams.
Drive sustainable process improvements through data-driven decision-making, root cause analysis, and the implementation of corrective and preventive actions.
Ensure that manufacturing processes consistently meet internal quality standards and customer specifications while remaining scalable and cost-effective.
Lead or actively contribute to cross-functional project teams focused on improving process efficiency, product quality, and cost performance.
Recommend and implement improvements to equipment, tooling, and work methods to increase throughput and optimize resource utilization.
Collaborate in the design and specification of new equipment and tooling to meet production and quality requirements.
Support the installation, testing, and optimization of new or modified equipment to ensure successful integration into manufacturing operations.
Assist in developing and refining manufacturing processes to improve repeatability, yield, and operational reliability.
Conduct root cause analyses of process issues and partner with Quality Engineers to implement sustainable corrective and preventive actions.
Collect and analyze production and process data to identify trends, deviations, and improvement opportunities.
Create clear, accurate process documentation including diagrams, workflows, and written instructions.
Draft and revise detailed work instructions and standard operating procedures (SOPs) with input from senior engineers.
Contribute to the development of validation documentation for new parts, design changes, and process updates.
Assist in managing nonconforming material by documenting issues, coordinating evaluations, and supporting disposition activities.
Interpret and apply tools such as Process Flow Diagrams (PFDs), Failure Mode and Effects Analyses (FMEAs), and Process Control Plans (PCPs) to ensure process control and risk mitigation.