Process/ Industrial Engineer

Myomo, Inc.; Burlington (MA); On-site; USD 90,000 - 115,000; Full time

Job summary

Myomo, Inc. in Burlington, MA is seeking an Industrial Engineer to optimize manufacturing operations using Lean principles and data-driven decision making. You will focus on process improvement, labor utilization, material flow, and facility layout to enhance safety, quality, delivery, and cost.

The role collaborates with Manufacturing, Quality, Supply Chain, Engineering, and Operations. The ideal candidate has 2–5 years in manufacturing or operations engineering, a Bachelor's in Industrial

Qualifications

• Bachelor's degree in Industrial Engineering or related engineering discipline.
• 2–5 years of experience in manufacturing, industrial engineering, or operations engineering.
• Experience with Lean Manufacturing and continuous improvement methodologies.
• Experience conducting time studies, labor analysis, line balancing, and workflow optimization.
• Excellent communication and project management skills.

Responsibilities

• Manufacturing Process Improvement: analyze processes to improve productivity, quality, safety, and efficiency.
• Production & Capacity Planning: evaluate capacity and optimize staffing and workflow.
• Manufacturing Support: partner with Manufacturing Engineering to improve processes and support new product introductions.
• Data Analysis: collect and present manufacturing metrics, develop dashboards and reports.
• Documentation & Compliance: maintain standard work, process maps, and documentation; support audits.
• Cross-Functional Collaboration: work with multiple teams to meet production goals and promote continuous improvement.

Skills

Lean Manufacturing

Time studies

Line balancing

Data analysis

Problem solving

Excel

Project management

Communication

Education

Bachelor's degree in Industrial Engineering

Tools

Power BI

Minitab

SQL

Python

Tulip MES

Job description

Industrial Engineer

Department: Manufacturing

Employment Type: Full Time

Location: Burlington, MA

Compensation: $90,000 - $115,000 / year

Description

Why should you join our success story?

Based on patented technology developed at MIT, Harvard Medical School and by the Company, Myomo develops and markets the MyoPro® product line of lightweight, non-invasive, powered arm braces (orthoses) to restore function in paralyzed or weakened arms and hands of individuals that have suffered a stroke, spinal cord, or nerve injury. (E.g. brachial plexus injury or other neuro-muscular disabilities.) It is the only device that, sensing a patient’s own neurological signals through non-invasive wearable sensors, can restore the ability to use their arms and hands so that they can live independently, increase their quality of life, reduce cost of care, and return to work. Published clinical research shows a clinically significant instantaneous reduction in upper extremity impairment with the MyoPro. Our technology has been referred by leading-edge rehabilitation facilities including Mayo Clinic, Kennedy Krieger Institute, Cleveland Clinic, Loma Linda Medical Center, Massachusetts General Hospital, numerous VA Hospitals, and more. Myomo is headquartered in Burlington, Massachusetts, with sales and clinical professionals across the U.S.

What we’re looking for:

The Industrial Engineer is responsible for improving manufacturing operations through the application of industrial engineering principles, Lean manufacturing methodologies, and data-driven decision making. This role focuses on optimizing manufacturing processes, labor utilization, material flow, production capacity, and facility layout to improve safety, quality, delivery, and cost. The Industrial Engineer works cross-functionally with Manufacturing, Quality, Supply Chain, Engineering, and Operations to identify improvement opportunities, implement sustainable solutions, and support operational excellence in a regulated medical device manufacturing environment.

Keys to success include curiosity, initiative, and a drive to unlock better systems and workflows, ultimately supporting optimal performance. Our ideal candidate is deeply positive, process-minded, and highly detailed, viewing this role as a vehicle to continually foster a culture of excellence.

How You'll Drive Impact:

Manufacturing Process Improvement:

• Analyze manufacturing processes to improve productivity, quality, safety, and efficiency.
• Conduct time studies, work measurement, and labor utilization analyses to establish standard work and optimize staffing levels.
• Lead continuous improvement initiatives utilizing Lean Manufacturing principles, including Value Stream Mapping, 5S, Standard Work, Visual Management, Kanban, and Kaizen events.
• Identify and eliminate waste while improving workflow, throughput, and manufacturing performance.
• Develop and monitor key manufacturing metrics to drive operational improvements.

Production & Capacity Planning:

• Evaluate production capacity and develop recommendations to support changing production demands.
• Perform line balancing and workflow optimization to maximize labor and equipment utilization.
• Analyze bottlenecks and recommend improvements to increase throughput.
• Support facility layout planning and material flow improvements.
• Develop labor standards and assist Operations with production planning.

Manufacturing Support:

• Partner with Manufacturing Engineering to improve existing manufacturing processes and support new product introductions.
• Support root cause investigations and implement corrective actions using structured problem-solving methodologies.
• Collaborate with Quality to implement and verify CAPA activities.
• Identify and lead cost reduction initiatives through process optimization and waste elimination.
• Evaluate equipment, tooling, fixtures, and automation opportunities to improve operational efficiency.

Data Analysis:

• Collect, analyze, and present manufacturing performance data.
• Develop dashboards and reports tracking productivity, labor efficiency, OEE, scrap, cycle time, and throughput.
• Perform statistical analyses to identify trends and quantify improvement opportunities.Present recommendations to leadership using data-driven analyses.

Documentation & Compliance:

• Develop and maintain manufacturing documentation, including standard work, process maps, work instructions, labor standards, and workflow diagrams.
• Support process validation activities as required.
• Ensure compliance with FDA Quality System Regulations (21 CFR Part 820), ISO 13485, and internal quality procedures.
• Participate in internal and external audits.

Cross-Functional Collaboration:

• Work closely with Manufacturing, Engineering, Supply Chain, Quality, and Operations to achieve production objectives.
• Train manufacturing personnel on standardized work and Lean methodologies.
• Participate in cross-functional improvement teams supporting strategic initiatives.
• Promote a culture of continuous improvement throughout the organization.

What You'll Bring:

• Bachelor's degree in Industrial Engineering or related engineering discipline.
• 2–5 years of experience in manufacturing, industrial engineering, or operations engineering.
• Experience with Lean Manufacturing and continuous improvement methodologies.
• Experience conducting time studies, labor analysis, line balancing, and workflow optimization.
• Strong analytical and problem-solving skills.
• Proficiency with Microsoft Excel and data analysis tools.
• Experience developing manufacturing KPIs and performance metrics.
• Familiarity with root cause analysis techniques (5 Whys, Fishbone, A3, 8D).
• Excellent communication and project management skills.

Preferred:

• Experience in medical device or other regulated manufacturing environments.
• Lean Six Sigma Green Belt or Black Belt certification.
• Experience with MES systems (Tulip preferred).
• Familiarity with process validation (IQ/OQ/PQ).
• Knowledge of statistical process control (SPC).
• Experience with facility layout planning and material flow analysis.
• Experience using Power BI, Minitab, SQL, or Python for data analysis.