

New · posted Nov 11
Johnson & Johnson · Medical Devices
Sr Eng Quality Engineering
- Jacksonville, FL
- On-site
- Full-time
- Senior & Principal
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.
The Senior Quality Engineer serves as a lead Quality Engineering contributor for the Jacksonville intraocular lens (IOL) manufacturing operation. The role provides hands-on quality oversight and advanced technical support for startup, technology transfer, qualification, validation, regulatory readiness, commercialization, and sustained manufacturing of Class III IOL products. The position partners with Operations, Manufacturing Engineering, Validation, Quality Systems, QC Laboratories, Supplier Quality, R&D, Regulatory Affairs, Facilities, EHS, IT, and Supply Chain to ensure that products, processes, equipment, software, test methods, utilities, and supporting systems are compliant, capable, and inspection ready.
The Senior Quality Engineer applies advanced quality engineering, statistical, risk management, investigation, and problem-solving methods throughout the product and process lifecycle. The role leads complex assignments with limited supervision, provides technical direction to project teams and junior engineers, and supports timely, independent quality decisions that protect patients, product quality, compliance, and supply continuity.
What you need
Preferred Skillsnice to have
AI Judgement Integration, Coaching, Consistency, Controls Compliance, Critical Thinking, Data Savvy, Engineering, Financial Competence, Good Automated Manufacturing Practice (GAMP), ISO 9001, Lean Supply Chain Management, Leverages Information, Process Improvements, Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy
Pay and benefits
$96,000 – $155,250 a year
Employer providedThe anticipated base pay range for this position is
$96,000.00 - $155,250.00
Pension and 401(k) savings plan
Long-term incentive program
Vacation (120 hours per year)
Sick time (40 hours per year)
13 paid holidays including floating holidays
Parental leave (480 hours)
Where you'll work
Jacksonville, FLOn-siteOpen in Maps (opens in a new tab)
More jobs in Jacksonville, FLWorking conditions
Job Function
Supply Chain Engineering
Job Sub Function
Quality Engineering
Job Category
Scientific/Technology
All Job Posting Locations
Jacksonville, Florida, United States of America
Equal opportunity, accessibility and legal noticesJohnson & Johnson's statements, word for word
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
For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits
Job intelligence
The context around this role
Live data · November 11, 2026
Salary intelligence
How the pay compares
This role's midpoint is 2% above the US median for Quality Engineering roles at this level.
This roleEmployer provided
Senior & Principal roles in the US103 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $96,000 | — | $155,250 |
| All US (middle half) | $104,500 | $123,500 | $138,500 |
This role: Johnson & Johnson's own published range. Comparisons: the base pay employers published on open Quality Engineering roles at the same level on Regulatory Jobs, November 11, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Engineering
The general path across 218 open Quality Engineering roles on Regulatory Jobs, with the titles they carry most. Not Johnson & Johnson's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 5 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance3
- Lab testing and methods3
- Quality systems and risk3
- Collaboration and leadership3
- Validation and qualification2
- Documentation and SOPs1
- Investigations and CAPA1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Engineering work in medical devices, led by the two this posting names, each linked to the agency or standards body that publishes it.
- ISOISO 9001(official source, opens in a new tab)Quality management systems requirementsNamed in the posting
- ISPEISPE GAMP 5(official source, opens in a new tab)A risk-based approach to compliant GxP computerized systemsNamed in the posting
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- IECIEC 62366-1(official source, opens in a new tab)Application of usability engineering to medical devices
- ISOISO 10993-1(official source, opens in a new tab)Biological evaluation of medical devices within a risk management process
- ISOISO 11135(official source, opens in a new tab)Ethylene oxide sterilization of health care products
- ISOISO 11137-1(official source, opens in a new tab)Radiation sterilization of health care products
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on medical devices
- FDAFDA Computer Software Assurance(official source, opens in a new tab)Risk-based assurance for production and quality system software
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- FDA21 CFR Part 806(official source, opens in a new tab)Reports of medical device corrections and removals
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
Company hiring pulse
Johnson & Johnson on Regulatory Jobs
- 42
- Open roles
- 42
- Distinct roles
- 18
- Locations
By discipline
- Quality25 60%
- Clinical9 21%
- Regulatory8 19%
By level
- Manager16 38%
- Senior & Principal15 36%
- Associate & Specialist7 17%
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Sr Eng Quality Engineering at Johnson & Johnson
Applications close November 24. $96K–$155K a year, employer provided.


