Industrial Engineer

Johnson & Johnson MedTech

Santa Clara (CA)

On-site

USD 75,000 - 121,000

Full time

2 days ago
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Benefits offered by this job

Vacation 120 hours per year
Sick time 40 hours per year
Holiday pay 13 days per year
Parental leave 480 hours

Job summary

Johnson & Johnson is recruiting an Industrial Engineer located in Santa Clara, CA to support manufacturing systems, process improvement, capacity planning, and layout design across NPI and sustaining operations for electro-mechanical and robotic medical device assembly.

The role requires applying industrial engineering principles, Lean methodologies, and data-driven analysis to improve productivity, quality, and regulatory compliance, with cross-functional collaboration and manufacturing

Qualifications

  • 2-4 years of industrial, manufacturing, or operations engineering experience in a regulated or high-volume manufacturing environment.
  • Knowledge of industrial engineering fundamentals including time studies, line balancing, capacity planning, labor analysis, and process flow optimization.
  • Experience supporting manufacturing process development, validation activities, or continuous improvement projects.
  • Familiarity with Lean Manufacturing principles, 5S, visual management, standardized work, and waste reduction.
  • Basic understanding of statistical analysis methods including SPC, capability studies, and problem-solving methodologies.
  • Experience creating or maintaining manufacturing documentation such as work instructions, standard operating procedures, and process flow documentation.
  • Ability to read and interpret engineering drawings, schematics, and bills of material.
  • Strong analytical and problem-solving skills.
  • Effective verbal and written communication skills and ability to work effectively in cross-functional teams.
  • Proficiency with Microsoft Excel and other data analysis tools.
  • Familiarity with CAD software for layout development and manufacturing visualization is preferred.

Responsibilities

  • Support industrial engineering activities for NPI and sustaining product lines, including process development, line layout, work cell design, and production flow analysis.
  • Perform takt time, cycle time, capacity, and staffing analyses to support production volume and operational goals.
  • Assist in the development and qualification of manufacturing processes, fixtures, tooling, and automation solutions in collaboration with manufacturing and design engineering teams.
  • Support process characterization studies, DOE, process validation (IQ/OQ/PQ), and test method validation activities.
  • Participate in continuous improvement initiatives focused on cost, quality, throughput, and lead-time reduction using Lean and Six Sigma methodologies.
  • Conduct time studies, motion studies, value stream mapping, and other industrial engineering analyses to identify opportunities for improvement.
  • Collect, analyze, and report manufacturing performance metrics such as yield, throughput, cycle time, and scrap to support operational decision making.
  • Create and maintain manufacturing documentation including work instructions, process flow diagrams, standard work, process control plans, and engineering change documentation.
  • Support root cause investigations and implementation of corrective and preventive actions.
  • Collaborate with cross-functional teams to support product launches, process transfers, and manufacturing readiness activities.
  • Assist with manufacturing data collection and reporting systems, including ERP, MES, and PLM platforms.

Skills

Analytical reasoning
CAPA
Emerging technologies
Execution focus
Gemba Kaizen
Issue escalation
Lean supply chain
Process control
Process engineering
Process oriented
Product improvements
Project engineering
Safety oriented
STEM application
Situational awareness
Technical research
Technologically savvy
Analytical
Computerized equipment skills
Excel proficiency

Education

Bachelor's degree in Industrial Engineering, Mechanical Engineering, Manufacturing Engineering or related technical field
Master’s degree in Industrial or Manufacturing Engineering preferred

Tools

CAD software
ERP/MES/PLM systems
FlexSim/Simio/Arena or equivalent

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, 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 jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

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 an Industrial Engineer located in Santa Clara, CA

About MedTech

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

Learn more at https://www.jnj.com/medtech

Position Summary

The Industrial Engineer will support manufacturing systems, process improvement, capacity planning, and layout design initiatives across New Product Introduction (NPI) and sustaining operations for electro-mechanical and robotic medical device assembly. Working closely with Manufacturing, Design, Quality, Supply Chain, and Supplier teams, this role will help develop and implement efficient, compliant, and scalable production systems.

The Industrial Engineer will apply industrial engineering principles, Lean methodologies, and data-driven analysis to improve productivity, quality, and operational performance while supporting compliance with applicable medical device regulations and quality system requirements.

In This Role You Will
  • Support industrial engineering activities for NPI and sustaining product lines, including process development, line layout, work cell design, and production flow analysis.
  • Perform takt time, cycle time, capacity, and staffing analyses to support production volume and operational goals.
  • Assist in the development and qualification of manufacturing processes, fixtures, tooling, and automation solutions in collaboration with manufacturing and design engineering teams.
  • Support process characterization studies, Design of Experiments (DOE), process validation (IQ/OQ/PQ), and test method validation activities.
  • Participate in continuous improvement initiatives focused on cost, quality, throughput, and lead-time reduction using Lean and Six Sigma methodologies.
  • Conduct time studies, motion studies, value stream mapping, and other industrial engineering analyses to identify opportunities for improvement.
  • Collect, analyze, and report manufacturing performance metrics such as yield, throughput, cycle time, and scrap to support operational decision making.
  • Create and maintain manufacturing documentation including work instructions, process flow diagrams, standard work, process control plans, and engineering change documentation.
  • Support root cause investigations and implementation of corrective and preventive actions.
  • Collaborate with cross-functional teams to support product launches, process transfers, and manufacturing readiness activities.
  • Assist with manufacturing data collection and reporting systems, including ERP, MES, and PLM platforms.
Qualifications
Education
  • Bachelor of Science degree in Industrial Engineering, Mechanical Engineering, Manufacturing Engineering, or related technical field required.
  • Master’s degree in Industrial or Manufacturing Engineering preferred.
Required
Experience and Skills
  • 2-4 years of industrial, manufacturing, or operations engineering experience in a regulated or high-volume manufacturing environment.
  • Knowledge of industrial engineering fundamentals including time studies, line balancing, capacity planning, labor analysis, and process flow optimization.
  • Experience supporting manufacturing process development, validation activities, or continuous improvement projects.
  • Familiarity with Lean Manufacturing principles, including 5S, visual management, standardized work, and waste reduction techniques.
  • Basic understanding of statistical analysis methods including SPC, capability studies, and problem-solving methodologies.
  • Experience creating or maintaining manufacturing documentation such as work instructions, standard operating procedures, and process flow documentation.
  • Ability to read and interpret engineering drawings, schematics, and bills of material.
  • Strong analytical and problem-solving skills.
  • Effective verbal and written communication skills and ability to work effectively in cross-functional teams.
  • Proficiency with Microsoft Excel and other data analysis tools.
  • Familiarity with CAD software for layout development and manufacturing visualization is preferred.
Preferred
  • Experience within a medical device, life sciences, electronics, or other regulated manufacturing environment.
  • Familiarity with medical device quality systems and regulatory requirements including GMP and ISO 13485.
  • Exposure to process validation activities (IQ/OQ/PQ), DOE, and risk assessment tools such as PFMEA.
  • Knowledge of simulation tools such as FlexSim, Simio, Arena, or equivalent.
  • Experience with ERP, MES, or PLM systems.
  • Lean or Six Sigma certification (Yellow Belt or equivalent).
  • Exposure to automation, robotics, or electro-mechanical assembly processes.
Other
  • Ability to travel up to 10% to manufacturing and supplier sites.
  • May be required to work in cleanroom or classified manufacturing environments and comply with applicable protocols.
Why Johnson & Johnson

Join a team where your engineering expertise will help shape the future of surgery and directly impact patient outcomes. We offer a collaborative environment, opportunities for professional growth, and the chance to work on meaningful, life-changing products.

Johnson & Johnson is an equal opportunity employer.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected under federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

If you are under 18 years of age you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check

Required Skills

Analytical Reasoning, Computerized Equipment Skills, Corrective and Preventive Action (CAPA), Emerging Technologies, Execution Focus, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Process Control, Process Engineering, Process Oriented, Product Improvements, Project Engineering, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Technical Research, Technologically Savvy

Preferred Skills:

Analytical Reasoning, Computerized Equipment Skills, Corrective and Preventive Action (CAPA), Emerging Technologies, Execution Focus, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Process Control, Process Engineering, Process Oriented, Product Improvements, Project Engineering, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Technical Research, Technologically Savvy

The anticipated base pay range for this position is :

$75,000.00 - $120,750.00

Additional Description For Pay Transparency

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Benefits
  • Vacation –120 hours per calendar year
  • Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
  • Holiday pay, including Floating Holidays –13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year
  • Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
  • Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
  • Caregiver Leave – 80 hours in a 52-week rolling period10 days
  • Volunteer Leave – 32 hours per calendar year
  • Military Spouse Time-Off – 80 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

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