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Senior Industrial Engineer

Job in Santa Clara, Santa Clara County, California, 95053, USA
Listing for: Johnson & Johnson
Full Time position
Listed on 2026-02-16
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 109000 - 174800 USD Yearly USD 109000.00 174800.00 YEAR
Job Description & How to Apply Below

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at

Job Function

Supply Chain Engineering

Job Sub Function

Process Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Santa Clara, California, United States of America

Job Description

Johnson & Johnson is recruiting for a Senior Industrial Engineer located in Santa Clara, CA

About Med Tech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at

Purpose

The Senior Industrial Engineer will lead and implement manufacturing systems, process improvement, capacity and layout design initiatives across NPI and sustaining operations for electro-mechanical and robotic medical device assembly. This role acts as a technical lead and change agent — partnering with Manufacturing, Design, Quality, Supply Chain, and Supplier teams to define and deploy robust, compliant, and efficient production systems. Responsibilities include process design and validation, labor/capacity modeling, value stream optimization, line balancing, cost reduction, and mentoring junior engineers.

The role requires strong application of Lean and Six Sigma methods, data-driven decision making, and alignment to medical device regulatory requirements (e.g., GMP, ISO 13485).

In this role you will
  • Lead end-to-end industrial engineering activities for NPI and sustaining product lines, including process design, factory/line layout, work cell design, and production flow.
  • Develop takt time, cycle time, and staffing models; create labor standards and line balancing to meet production volume and quality targets.
  • Design and qualify manufacturing and test processes, fixtures, tooling, and automation concepts in collaboration with manufacturing and design engineering.
  • Create and implement process characterization, design of experiments (DOE), process validation (IQ/OQ/PQ), and test method validation (TMV) protocols and reports.
  • Drive continuous improvement projects (cost, quality, lead time) using Lean, Kaizen, and Six Sigma methodologies; quantify and realize cost and productivity benefits.
  • Apply industrial engineering methods (time studies, motion studies, value stream mapping, simulation) to optimize throughput, ergonomics, and safety.
  • Establish and monitor key manufacturing metrics (yield, OEE, throughput, scrap) and apply SPC to control and improve processes.
  • Develop and maintain manufacturing documentation (work instructions, process control plans, PFMEA, ECOs, DHRs, MPIs) that meet internal and regulatory expectations.
  • Coach and mentor junior industrial/manufacturing engineers; influence multi-functional teams and suppliers to deliver on schedule and quality.
  • Support risk assessments and statistical analyses to inform design-for-manufacturing decisions and product launch readiness.
  • Collaborate with IT/automation teams to integrate MES/ERP/PLM systems and support data collection for process improvement.
Qualifications Education
  • Bachelor of Science degree in Industrial Engineering, Mechanical Engineering, Manufacturing Engineering, or a related technical field required.
  • Master’s degree in Industrial/Manufacturing Engineering or related field preferred.
Experience and Skills Required
  • 6+ years of industrial/manufacturing engineering experience in a high-mix, regulated manufacturing environment (medical device, automotive, electronics, or similar).
  • Demonstrated expertise in line balancing, capacity planning, takt/cycle time analysis, work measurement, and labor standards.
  • Strong experience leading process development and validation activities (IQ/OQ/PQ), DOE, and process characterization.
  • Consistent record driving Lean and continuous improvement initiatives; familiarity with Kaizen, 5S, SMED.
  • Proficiency in statistical methods and tools (SPC, capability analysis, hypothesis testing); experience with Minitab, JMP, or equivalent.
  • Experience authoring and maintaining PFMEA, process control plans, work instructions, and manufacturing documentation.
  • Ability to read and interpret engineering drawings, schematics, and BOMs.
  • Strong problem-solving skills with experience in root cause analysis tools (5 Whys, Fishbone, 8D).
  • Effective written and verbal communication skills; proven ability to influence multi-functional collaborators.
  • Experience with CAD for basic layout and tooling concepting (e.g., Solid Works, AutoCAD) and familiarity with manufacturing simulation tools (e.g., Arena, Flex Sim) is…
Position Requirements
10+ Years work experience
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