New · posted Oct 28
Johnson & Johnson · Medical Devices
Principal Quality Engineer
- New Brighton, MN
- On-site
- Full-time
- Senior & Principal
The role
The Principal Quality Engineer (Design Assurance) is responsible for ensuring medical devices are designed, developed, and transferred to manufacturing in compliance with applicable quality system and regulatory requirements. This role partners closely with R&D, Manufacturing, Regulatory Affairs, Clinical Affairs, and Marketing to provide hands-on Design Assurance support throughout new product development. This role applies and interprets relevant medical device standards and regulations as they relate to design and development activities, advising design teams on the quality and compliance impacts of design decisions. Operating with a high degree of autonomy, the Principal Quality Engineer is expected to influence design assurance strategy across programs, provide mentoring and technical guidance to senior engineers, and serve as a subject matter expert during regulatory interactions. This role provides practical, execution‑focused quality engineering support with an emphasis on risk management, verification and validation oversight, and design transfer, enabling timely and compliant product launches.
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.
Johnson & Johnson is hiring for a Principal Quality Engineer (Design Assurance) to support the Shockwave Reducer business located in New Brighton, MN.
Cardiovascular Solutions from Johnson & Johnson
Across Johnson & Johnson, we are tackling the world’s most complex and pervasive health challenges. Through a cardiovascular portfolio that provides healthcare professionals with advanced mapping and navigation, miniaturized tech, and precise ablation, we are addressing conditions with significant unmet needs such as heart failure, coronary and peripheral artery disease, stroke, and atrial fibrillation. We are the global leaders in heart recovery, circulatory restoration and the treatment of heart rhythm disorders, as well as an emerging leader in neurovascular care, committed to taking on two of the leading causes of death worldwide in heart failure and stroke. For more information on circulatory restoration, visit our website.
What you need
- Bachelor’s degree in Biomedical/ Mechanical, or related Engineering discipline with 10+ years of experience in the medical device industry, or Master’s degree with 8+ years of experience
- Demonstrated progression providing technical leadership across multiple complex development programs, including hands-on experience across
- Design Verification and Validation (V&V), including review and approval of protocols and reports
- Test Method Validation (TMV), including development, execution, or quality oversight of validated methods
- Risk Management in accordance with ISO 14971
- Failure Modes and Effects Analysis (FMEA) development and management
- Application of FDA GMP and ISO 13485 requirements within a design and development environment
- Demonstrated ability to independently interpret and apply applicable medical device quality system and regulatory requirements as they relate to design and development activities, including ISO 13485, ISO 14971, 21 CFR Part 820 / FDA QMSR, and EU MDR (2017/745)
- Strong statistical and analytical skills, including hypothesis testing, sample size determination, and data analysis
- Proficiency with statistical software (e.g., Minitab or equivalent)
- Strong technical writing skills for quality-related documentation, including protocols, reports, and design history records
- Demonstrated ability to manage multiple complex development activities simultaneously while maintaining attention to detail and compliance
- Acts as a Principal-level technical authority, providing coaching and informal mentorship to Senior and mid-level Quality Engineers and influencing cross-functional decision-making.
- Self-directed and accountable, with the ability to independently execute assigned responsibilities and follow through on commitments
- Experience supporting regulatory inspections and audits (FDA, Notified Body, ISO) through preparation, participation, and response development
- Clear and effective communicator, able to convey technical and quality concepts to diverse audiences
- Willingness to travel up to 10% of the time
- Ability to lift objects up to 25 lbs
Preferred Qualificationsnice to have
- Experience supporting development of Class II or Class III medical devices, preferably within cardiovascular or interventional product areas
- Familiarity with balloon catheter, interventional, or sterile single-use devices
- Experience contributing to quality activities supporting regulatory submissions (e.g., 510(k), CE Technical Files, PMA modules)
- Working experience supporting biocompatibility and sterilization activities within a design and development environment
- Hands-on experience with PLM systems (e.g., Windchill) and manufacturing execution systems (MES)
- Experience supporting manufacturing readiness and transfer activities for new product introductions, including associated validation efforts
- Knowledge of human factors and usability engineering principles (e.g., IEC 62366-1)
- Lean, Six Sigma or Design for Six Sigma certification
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, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
Preferred Skillsnice to have
Coaching, Controls Compliance, Critical Thinking, Engineering, Fact-Based Decision Making, Financial Competence, ISO 9001, Lean Supply Chain Management, Non-Conformance Reporting (NCR), Organizing, Process Improvements, Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application
Pay and benefits
$102,000 – $177,100 a year
Employer providedThe anticipated base pay range for this position is
$102,000.00 - $177,100.00
401(k) savings plan
Pension plan
Long-term incentive program
Vacation (120 hours per year)
13 paid holidays
Parental leave (480 hours)
Where you'll work
New Brighton, MNOn-siteOpen in Maps (opens in a new tab)
More jobs in New Brighton, MNWorking conditions
Job Function
Supply Chain Engineering
Job Sub Function
Quality Engineering
Job Category
Scientific/Technology
All Job Posting Locations
New Brighton, Minnesota, United States of America
Essential Job Functions
Lead quality assurance for new product development
- Partner with design teams to ensure compliance with ISO 13485 and applicable regulatory requirements
- Serve as technical subject matter expert on regulatory standards, statistical methods, test design, and acceptance criteria
- Participate in design reviews to provide an independent perspective on compliance and risk
- Ensure Design History Files (DHFs) are complete, accurate, and inspection-ready throughout the development lifecycle
- Develop and maintain Risk Management Files including plans/reports, hazard analyses, FMEAs, risk control strategies, and risk assessments
- Support development and execution of incoming inspection plans, first article inspections (FAI), and related documentation to ensure alignment with design intent
- Advise design teams on quality system and regulatory implications of design decisions and changes
- Provide Design Assurance oversight for Verification and Validation (V&V) activities
- Review and approve protocols, test methods, and reports
- Provide quality oversight to ensure test strategies, acceptance criteria, and sample sizes are appropriate and compliant with applicable standards
- Serve as a quality advisor for V&V activities including biocompatibility, sterilization validation, packaging validation, and shelf‑life studies
- Lead or support test method validation (TMV) activities to ensure methods are suitable for their intended use and comply with internal and regulatory expectations
- Perform or witness hands-on Design V&V testing when needed to support design assurance assessments
- Partner with to Manufacturing and Operations on design transfer and validation
- Support equipment and process validation activities (IQ/OQ/PQ) associated with new product introduction
- Ensure manufacturing processes, controls, and validations support design intent and regulatory requirements
- Support Contract Manufacturing and Supplier Quality in identifying, qualifying, and managing suppliers to support new product development and design transfer
- Participate in FDA, Notified Body, and ISO 13485 audits/inspections
- Contribute to regulatory submissions (510(k), CE Technical Files, PMA modules)
- Understand and apply Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team
- Perform additional duties as assigned
Equal opportunity, accessibility and legal noticesJohnson & Johnson's statements, word for word
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)).
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
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
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.
Job intelligence
The context around this role
Live data · October 28, 2026
Salary intelligence
How the pay compares
This role's midpoint is 14% above the US median for Quality Assurance roles at this level.
This roleEmployer provided
Senior & Principal roles in Minnesota22 roles publishing pay
Senior & Principal roles in the US323 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $102,000 | — | $177,100 |
| Minnesota (middle half) | $92,250 | $100,750 | $117,000 |
| All US (middle half) | $104,000 | $122,000 | $142,250 |
This role: Johnson & Johnson's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 961 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Johnson & Johnson's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance6
- Collaboration and leadership6
- Validation and qualification4
- Quality systems and risk4
- Lab testing and methods3
- Documentation and SOPs3
- Regulatory submissions2
- Investigations and CAPA1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices
- European UnionEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Risk management for medical devices
- FDAFDA 510(k)(official source, opens in a new tab)Premarket notification for medical devices
- FDAFDA PMA(official source, opens in a new tab)Premarket approval for class III medical devices
Company hiring pulse
Johnson & Johnson on Regulatory Jobs
- 45
- Open roles
- 44
- Distinct roles
- 22
- Locations
By discipline
- Quality31 69%
- Regulatory11 24%
- Compliance & Safety3 7%
By level
- Associate & Specialist16 36%
- Senior & Principal15 33%
- Manager11 24%
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Principal Quality Engineer at Johnson & Johnson
Open until filled. $102K–$177K a year, employer provided.