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New · posted Nov 3

Johnson & Johnson · Medical Devices

Design Quality Engineer II

  • Warsaw, IN
  • On-site
  • Full-time
  • Associate & Specialist
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EmploymentFull-time
DeadlineCloses Nov 23, 2026

The role

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.

Depuy Synthes is the largest, most innovative, and comprehensive orthopaedic business in the world.

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

DePuy Synthes is recruiting for two new Design Quality Engineer II team members for our Warsaw, IN location.

Applies basic Quality Engineering/Scientific Method techniques and principles to daily tasks and activities. In addition, applies relevant regulations, standards, and industry best practices to assignments. Participates in and performs tasks on projects and assignments with technical responsibility or strategic input. Receives intermittent, detailed instructions from technical Quality leaders at various levels, in addition to other stakeholders.

DUTIES & RESPONSIBILITIES*

In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Demonstrates competency to apply various tools and methods (for example, Six Sigma, Lean) to identify and realize new product or process introductions as well as process improvements.

• Demonstrates competency to apply various risk management and risk mitigation tools and practices (for example, mistake proofing, critical control points, failure mode, and effects analysis).

• Contributes to the reliability assessments of product design.

• Contributes to root cause investigations using various problem solving techniques and tools, and assesses effectiveness of corrective actions.

• Conducts, and supports the development of, test methods in equipment, process, and product qualifications/validations.

• Ensures that process Quality control plans are in accordance with product risk level and are consistently followed.

• Contributes to, implements, and/or maintains, production and process controls using appropriate techniques (for example, process capability measures, statistical process controls, and process performance metrics).

• Participates in technical reviews as appropriate.

• Responsible for communicating business related issues or opportunities to next management level

• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.

• For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable

• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures

• Performs other duties assigned as needed

EXPERIENCE AND EDUCATION*

• Bachelor’s degree (or equivalent) in Engineering or related technical/scientific field AND 2 or more years related experience.

• Basic knowledge of Quality Engineering/Scientific methods and techniques.

• Basic technical understanding of manufacturing equipment and processes.

• Experience managing tasks or small projects and demonstrating project leadership abilities.

Basic understanding of and application of measuring techniques (for example, mechanical, optical, gages, automation

REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS*

• Production and Processing Systems

• Qualification and Validation

• Product Design Support

• Quality Statistics, Data Analysis and Tools

• Product Control and Disposition

• Product Development Support

• Technical Transfer & Scale Up

• Predictive Analytics / Reliability

ADDITIONAL POSITION REQUIREMENTS

• Ability to work in stressful/fast paced environment

• Ability to work and interact with co-workers to accomplish company goals in a team environment

• Management Skills

• Analytical/Problem Solving Skills

• Ability to communicate verbally and in writing

Position Requirement

• Standing (__15_%)

• Sitting (__70_%)

• Walking (_15__%)

SAFETY TESTS

•Bloodborne Pathogen

What you need

Preferred Skillsnice to have

Agility Jumps, Business Behavior, Compliance Management, Continuous Improvement, Database Backup, Data Gathering and Analysis, Data Savvy, Disruptive Innovations, Execution Focus, Issue Escalation, Process Oriented, Product Improvements, Quality Control (QC), Quality Control Testing, Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Report Writing

Where you'll work

Warsaw, INOn-siteOpen in Maps (opens in a new tab)

More jobs in Warsaw, IN

Working conditions

Job Function

Quality

Job Sub Function

R&D/Scientific Quality

Job Category

Professional

All Job Posting Locations

Warsaw, Indiana, United States of America

Job intelligence

The context around this role

Live data · November 3, 2026

Salary intelligence

How the pay compares

Associate & Specialist roles in the US24 roles publishing pay

Middle half $67,500 to $91,625, median $77,000
Annual base pay
Annual base payLowMedianHigh
All US$67,500$77,000$91,625

Comparisons: the base pay employers published on open Validation & CQV roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Validation & CQV

The general path across 126 open Validation & CQV roles on Regulatory Jobs, with the titles they carry most. Not Johnson & Johnson's own promotion track.

  1. This role

    Associate & Specialist

    Often: Associate QA Validation Specialist · Validation Analyst

    $77K median34 open
  2. Next step

    Senior & Principal

    Often: Senior Validation Engineer · Engineer III, Validation

    $121K median70 open
  3. Later

    Manager

    Often: Validation Manager · Manager Quality Assurance Validation

    $140K median14 open
  4. Later

    Director

    Often: Associate Director · Director, Computer System Quality Team Lead

    $232K median6 open
  5. Later

    VP & Executive

    Often: Head of Validation · Head of Validation & Risk Management

Skills DNA

What this role leans on

How many of the posting's 47 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 4 linesLab testing and methods: 7 linesDocumentation and SOPs: 4 linesInvestigations and CAPA: 1 lineValidation and qualification: 2 linesQuality systems and risk: 3 linesCollaboration and leadership: 6 linesGMPLab testingDocumentationInvestigationsValidationQuality systemsTeamwork
  • Lab testing and methods7
  • Collaboration and leadership6
  • GMP and compliance4
  • Documentation and SOPs4
  • Quality systems and risk3
  • Validation and qualification2
  • Investigations and CAPA1

Company hiring pulse

Johnson & Johnson on Regulatory Jobs

41
Open roles
41
Distinct roles
17
Locations

By discipline

  • Quality21 51%
  • Clinical13 32%
  • Regulatory7 17%

By level

  • Senior & Principal12 29%
  • Manager11 27%
  • Associate & Specialist11 27%
See all 41 Johnson & Johnson roles

More roles at Johnson & Johnson

All 41 Johnson & Johnson roles

Similar Validation & CQV roles elsewhere

Design Quality Engineer II at Johnson & Johnson

Applications close November 23.

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