Johnson & Johnson Posted October 30, 2026

Senior Mechatronics Engineer

Santa Clara, United States Full time
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About this opportunity

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 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:

Manufacturing Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Milpitas, California, United States of America, Santa Clara, California, United States of America

Job Description:

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 https://www.jnj.com/medtech

The Senior Mechatronics Engineer will lead the design, development, integration, verification, and lifecycle support of complex systems and equipment in a regulated MedTech environment. The role integrates mechanical design, electrical and electronic design, controls, software, sensing, motion, robotics, machine vision, instrumentation, and automation to deliver safe, reliable, maintainable, and scalable equipment solutions.

This engineer will provide technical ownership from stakeholder needs and system requirements through architecture, detailed design, prototyping, integration, verification, validation, deployment, and change control. The role requires hands-on engineering capability, strong system-level judgment, and effective leadership across internal functions and external equipment suppliers.

Key Responsibilities

·   Lead complete mechatronic system and equipment development from requirements and concept selection through architecture, detailed design, integration, verification, validation, release, and lifecycle support.

·   Translate user and stakeholder needs into clear, testable system, subsystem, interface, and equipment requirements with measurable acceptance criteria and appropriate traceability.

·   Develop and assess engineering concepts using feasibility studies, technical trade studies, rapid prototypes, proof-of-concept testing, and risk-based decision making.

·   Design and integrate mechanical structures and mechanisms, electrical/electronic hardware, sensors, actuators, motors, servo systems, pneumatics, controls, software, robotics, machine vision, instrumentation, and data-acquisition subsystems.

·   Create and review mechanical models, assemblies, drawings, tolerances, schematics, PCB designs, wiring diagrams, bills of material, interface definitions, and system specifications.

·   Perform engineering analysis including tolerance analysis, component sizing, motion and load analysis, reliability assessment, failure-mode evaluation, and design-for-manufacturability/serviceability reviews.

·   Plan and execute system integration, design verification, and validation activities; develop test methods, protocols, fixtures, automated tests, data analysis, and objective acceptance criteria.

·   Lead multidisciplinary troubleshooting and root-cause analysis across mechanical, electrical, controls, software, sensing, communications, and product/equipment interfaces.

·   Apply design controls, DFMEA/FMEA, hazard analysis, machine-safety principles, fault analysis, risk controls, and documented design reviews throughout development.

·   Develop robust equipment architectures with interlocks, diagnostics, error handling, fault recovery, calibration, maintainability, and serviceability.

·   Provide technical direction to system integrators, equipment suppliers, and technology partners through specifications, design reviews, supplier risk management, FAT/SAT, qualification, and acceptance.

·   Support equipment qualification, applicable process validation, technology transfer, manufacturing readiness, production ramp, engineering change control, obsolescence management, and lifecycle improvements.

·   Mentor engineers and technicians and contribute to common design standards, reusable architectures, engineering tools, technology roadmaps, and lessons learned.

Leadership and Collaboration Expectations

·   Independently own technically complex equipment or major system/subsystem development workstreams.

·   Lead architecture, design, integration, verification, and technical risk reviews using requirements, data, and engineering fundamentals.

·   Identify technical and interface risks early, establish mitigation plans, and drive issues to documented closure.

·   Influence R&D, Systems Engineering, Quality, Manufacturing, Operations, Regulatory, Supply Chain, Service, and external suppliers without relying on formal authority.

·   Communicate designs, trade-offs, risks, test results, and recommendations clearly to both technical and non-technical stakeholders.

·   Mentor less-experienced engineers and technicians while promoting engineering rigor, modularity, standardization, and design reuse.

Required Qualifications

·   Bachelor's degree in Mechatronics Engineering, Mechanical Engineering, Electrical Engineering, Robotics Engineering, Controls Engineering, or a closely related engineering discipline.

·   A minimum of 5 years of relevant experience developing multidisciplinary systems, automation, robotics, medical-device equipment, or production/test equipment.

·   Demonstrated experience completing multiple stages of the system or equipment design and development lifecycle.

·   Demonstrated ability to integrate mechanical, electrical/electronic, sensing, controls, and software elements into functioning equipment.

·   Hands-on experience with sensors, actuators, motors, motion systems, instrumentation, electrical hardware, and associated controls.

·   Strong system integration, verification, troubleshooting, and structured root-cause-analysis capability.

·   Experience developing engineering requirements, specifications, drawings, schematics, interface definitions, test methods, protocols, and technical reports.

·   Experience applying technical risk management, verification methods, configuration/change control, and disciplined design reviews.

·   Ability to work effectively across engineering disciplines and provide technical direction to suppliers or integration partners.

Preferred Qualifications

·   Master's degree in Mechatronics, Robotics, Mechanical Engineering, Electrical Engineering, Systems Engineering, Controls Engineering, or a related discipline.

·   Experience developing systems or equipment in medical devices or another highly regulated industry.

·   Experience with design controls, requirements traceability, equipment qualification, and risk management in accordance with applicable quality-system practices.

·   Experience with servo motion, robotics, machine vision, precision mechanisms, industrial controls, data acquisition, instrumentation, and industrial communications.

·   Experience with Rockwell Automation/Allen-Bradley, Siemens, Beckhoff, National Instruments, Cognex, Keyence, Universal Robots, FANUC, ABB, or comparable platforms.

·   Working knowledge of FDA quality-system expectations, ISO 13485, ISO 14971, GMP, machine safety, equipment qualification, and engineering change control.

·   Experience leading equipment suppliers, system integrators, contract manufacturers, or external development partners.

Required Technical Skills

·   SolidWorks: proficient mechanical equipment design, 3D parts and assemblies, engineering drawings, tolerance definition, configuration management, and design for manufacture and assembly.

·   Altium Designer: working capability in electrical schematic capture, PCB layout/design review, component libraries, design outputs, and electrical/electromechanical interface development.

·   Python: practical use for engineering automation, equipment and instrument integration, test sequencing, data acquisition, data analysis, troubleshooting tools, or verification applications.

·   Mechatronic system architecture: requirements allocation, interface management, component selection, trade studies, integration planning, and system-level verification.

·   Electrical and controls integration: sensors, actuators, motors, servo/stepper motion, safety circuits, industrial I/O, communications, instrumentation, and control-panel interfaces.

·   Automation technologies: PLC-based controls, robotics, machine vision, data acquisition, and automated test or manufacturing equipment.

·   Engineering methods: DFMEA/FMEA, hazard and fault analysis, tolerance analysis, root-cause analysis, verification and validation, reliability, and design reviews.

Soft Skills

·   Strong systems thinking, technical ownership, and accountability.

·   Analytical, hands-on, and structured problem solving.

·   Clear technical communication and disciplined documentation.

·   Effective cross-functional collaboration and ability to influence without formal authority.

·   Sound engineering judgment across performance, safety, quality, compliance, schedule, cost, and lifecycle considerations.

·   Supplier leadership, technical mentoring, adaptability, and curiosity about emerging technologies.

Travel Requirements

Approximately 10-20% travel, depending on project needs. Travel may include equipment suppliers, development partners, manufacturing sites, contract manufacturers, installation locations, and FAT/SAT or other acceptance activities.

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 by 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:

Preferred Skills:

Accelerating, Coaching, Compliance Risk, Critical Thinking, Facility Management, Good Manufacturing Practices (GMP), Lean Manufacturing Principles, Lean Supply Chain Management, Manufacturing Engineering, Performance Measurement, Product Design, Program Management, Project Engineering, Project Schedule, Robotic Automation, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy

The anticipated base pay range for this Bay Area position is:

$111,000.00 - $178,250.00

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)).

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off 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

Job details

Seniority
Senior
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Santa Clara, United States
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 645 comparable Senior Manufacturing & CMC roles across 84 biopharma companies.

645Comparable roles tracked
596Currently active
84Companies hiring similar roles
30Countries represented

Salary context

238 of 645 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $111,000/yr – $178,250/yr
Lowest disclosed · Senior Technician Calibration - Maintenance · Mylan Technologies, Inc. $37,000/yr – $80,000/yr
Peer group range $58,500 – $215,300 (median $151,700)

Where these roles are based

Top locations among the 645 comparable roles

United States434
India45
Ireland26
Netherlands19
United Kingdom11
Switzerland11

+ 24 more countries

Seniority mix

645 of 645 peers have a known seniority level

Senior401
Principal134
Associate Director110

Therapeutic area mix

2 of 645 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Dermatology & Aesthetics1
Vaccines & Infectious Disease1

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.