Senior Design Quality Engineer, NPD

Posted Yesterday
Be an Early Applicant
Santa Clara, CA, USA
In-Office
125K-201K Annually
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Leads design quality engineering for medical device new product development, from concept through launch and steady-state. Develops product requirements, verification and validation strategies, inspection and sampling plans, test methods, reliability strategies, and risk-management approaches. Ensures compliance with GMP, ISO, FDA design controls, and internal procedures while supporting statistical analysis, defect prevention, continuous improvement, and document approvals. Requires collaboration across engineering, manufacturing, quality, and validation teams, with up to 25% domestic and international travel.
Summary Generated by Built In

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:

R&D Product Development

Job Sub Function:

R&D Software/Systems Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Santa Clara, California, United States of America

Job Description:

The Senior Design Quality Engineer, New Product Development, will be responsible for providing quality engineering support and leadership for New Product Development. 

Responsibilities: 

  • Launch and stabilize new product launches through concept, design, development, and steady-state processes. 
  • Drives the development of product requirements, verification strategies, and validation strategies. 
  • Ensures new product development compliance to GMP (Good Manufacturing Practices), ISO (International Organization for Standardization) and any other applicable standards 
  • Activities would drive prevention, detection of defects at earliest phase of product design, continuous improvement & customer satisfaction. 
  • Proactively engage partners to drive consensus and resolve issues in a timely fashion. 
  • Provide statistical support and expertise and analytical problem solving for product development and manufacturing. 
  • Review and approve design control, manufacturing, quality, engineering and validation / qualification documents for conformance business practices and departmental procedures. 
  • Develop inspection and sampling plans, test methods, and transfer functions for products and components. 
  • Provide support and expertise in developing and executing a reliability strategy during new product development. 
  • Conducts projects and assignments with technical responsibility. 

Basic Qualifications 

Required: 

  • Bachelor’s Degree in Engineering from an accredited engineering school or related science field 
  • At least 5 years of quality experience 
  • New product development experience 
  • GD&T knowlegde 
  • Experience in medical device industry or other highly regulated field 
  • Advanced knowledge of Quality Engineering/Scientific methods and techniques and applied statistics of increasing complexity 
  • Previous work experience engaging in a team-based environment 
  • Ability to travel up to 25% Moderate domestic and international 

Preferred: 

  • Advanced Degree 
  • Experience with medical electrical-mechanical systems 
  • Knowledge of FDA requirements for design control of medical devices, particularly with verification and validation of software for medical electrical equipment. 
  • ASQ Certified Quality Engineer, ASQ Certified Reliability Engineer, and a Green Belt in one or more of the Process Excellence roadmaps (DMADVV, DMAIIC, or Lean) 
  • Experience driving risk management discussions, particularly as it relates to cascading identified product issues/hazards into potential user harms 
  • Prior software quality engineering experience in a product development environment 

Required Skills:



Preferred Skills:

Analytical Reasoning, Quality Compliance, Quality Control (QC), Quality Planning, Quality Tools, Quality Validation, Risk Analysis

The anticipated base pay range for this position is :

$125,000.00 - $201,250.00

Additional Description for Pay Transparency:

Please provide the benefits applicable. Required for US Positions. Please copy and paste the applicable benefits into the empty text box below, based on the type of role.
[DELETE ANY BENEFITS NOT APPLICABLE TO THE POSITION]
Please use the following language:
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)).
This position is eligible to participate in the Company’s long-term incentive program.
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

Skills Required

  • Bachelor's degree in engineering from an accredited engineering school or a related science field
  • At least 5 years of quality experience
  • New product development experience
  • Knowledge of GD&T
  • Experience in the medical device industry or another highly regulated field
  • Advanced knowledge of quality engineering and scientific methods and techniques
  • Applied statistics experience of increasing complexity
  • Previous experience working in a team-based environment
  • Ability to travel up to 25% domestically and internationally
  • Advanced degree
  • Experience with medical electrical-mechanical systems
  • Knowledge of FDA medical device design-control requirements, including software verification and validation for medical electrical equipment
  • ASQ Certified Quality Engineer certification
  • ASQ Certified Reliability Engineer certification
  • Green Belt in DMADVV, DMAIIC, Lean, or another Process Excellence roadmap
  • Experience leading risk-management discussions involving product issues, hazards, and potential user harms
  • Prior software quality engineering experience in a product development environment

Johnson & Johnson Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Johnson & Johnson and has not been reviewed or approved by Johnson & Johnson.

  • Healthcare Strength Healthcare coverage is characterized as comprehensive across medical, dental, and vision, with added supports like onsite clinics, fitness centers, and Employee Assistance resources. Mental-health services and wellbeing reimbursements are also described as meaningful components of the overall package.
  • Retirement Support Retirement offerings are portrayed as a major differentiator, combining a 401(k) with employer matching and an employer-funded pension plan. Stock options and other long-term financial supports are also positioned as part of the broader rewards mix.
  • Parental & Family Support Family-related benefits are presented as notably strong, including paid parental leave for all new parents and additional leave types for caregiving and bereavement. Financial assistance for adoption, fertility treatment, and surrogacy is highlighted as a significant support.

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The Company
HQ: New Brunswick, NJ
143,612 Employees
Year Founded: 1886

What We Do

Profound Change Requires Boldness. Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years. The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world. Social Media Community Guidelines: http://www.jnj.com/social-media-community-guidelines

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