

New · posted Nov 11
Johnson & Johnson · Medical Devices
Sr Supv Quality Control
- Jacksonville, FL
- On-site
- Full-time
- Manager
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.
Responsible for leading and coordinating the day-to-day operations of the Jacksonville IOL Quality Control, Quality Inspection, Testing, and Product Release functions. The position ensures timely and compliant incoming inspection, in-process inspection and testing, finished-product testing, batch/lot record review, disposition, and release of IOL products in accordance with approved procedures, production schedules, Johnson & Johnson policies, and applicable regulatory requirements.
The IOL Quality Control Senior Supervisor provides technical and people leadership across analytical, physical, optical, dimensional, and visual inspection activities. Responsibilities include test method transfer, verification and validation; First Article Inspection (FAI); laboratory equipment qualification and lifecycle management; data integrity; OOS/OOT and deviation investigations; reference standard and reagent controls; and continued improvement of laboratory and product-release systems.
The role is accountable for the end-to-end product release process within delegated authority, including confirmation that required manufacturing, inspection, testing, environmental or microbiological results, deviations, nonconformances, and associated quality records are complete, acceptable, and approved before final disposition. The Senior Supervisor partners with Quality Assurance, Manufacturing, Engineering, R&D, Regulatory Affairs, Supply Chain, Microbiology, Validation, and Planning to protect compliance, patient safety, product quality, and supply continuity.
The position develops laboratory and inspection associates through coaching, performance management, technical qualification, succession planning, and a strong culture of safety, compliance, inclusion, and continuous improvement.
What you need
Preferred Skillsnice to have
AI solution evaluation, Compliance Management, Controls Compliance, Corrective and Preventive Action (CAPA), Developing Others, Econometric Models, Inclusive Leadership, ISO 9001, Leadership, Operational Excellence, Performance Measurement, Quality Control (QC), Quality Control Testing, Quality Standards, Standard Operating Procedure (SOP), Strategic Thinking, Team Management, 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
Holiday pay (13 days)
Parental leave
Where you'll work
Jacksonville, FLOn-siteOpen in Maps (opens in a new tab)
More jobs in Jacksonville, FLWorking conditions
Job Function
Quality
Job Sub Function
Quality Control
Job Category
People Leader
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
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 9% above the US median for Quality Control roles at this level.
This roleEmployer provided
Manager roles in the US35 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $96,000 | — | $155,250 |
| All US (middle half) | $103,250 | $115,500 | $139,000 |
This role: Johnson & Johnson's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, November 11, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 265 open Quality Control 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 7 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance5
- Lab testing and methods5
- Documentation and SOPs3
- Investigations and CAPA3
- Validation and qualification3
- Collaboration and leadership3
- Quality systems and risk1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Control work in medical devices, led by the two this posting names, each linked to the agency or standards body that publishes it.
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and AnswersNamed in the posting
- ISOISO 9001(official source, opens in a new tab)Quality management systems requirementsNamed 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 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on medical devices
- ISOISO 10993-1(official source, opens in a new tab)Biological evaluation of medical devices within a risk management process
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- 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
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ASTMASTM F1980(official source, opens in a new tab)Accelerated aging of sterile barrier systems and medical devices
- ISOISO 11135(official source, opens in a new tab)Ethylene oxide sterilization of health care products
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 Supv Quality Control at Johnson & Johnson
Applications close November 24. $96K–$155K a year, employer provided.


