New · posted Oct 14
Johnson & Johnson · Medical Devices
Quality Operations Technician
- Irving, TX
- On-site
- Full-time
- Associate & Specialist
Closes Oct 21, 2026 · 8 days left
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.
You will be responsible for
- Supports v Quality Operation functions including: CAPA/NC initiatives, Quality “presence” on the manufacturing floors, and proactive GDP and Data Integrity.
- Assist with data collection for quality metrics, quality improvement initiatives, CAPAs, NCs, or Quality Systems.
- Conduct failure investigations and root cause analysis.
- Perform data searches and transactions within MES, JDE, and EtQ.
- Partner with QEs and business partners (and other NC “owners”) providing support with NC process, investigations, and/or corrective actions.
- Actively influence the team and other fellow workers as role model for Collaboration and Teamwork
- Provide BOP, Internal audit and external audit support.
- Read and interpret drawings, QCIC's and test methods and perform the tasks defined therein.
- Develop, prepare and report technical information to identify, segregate and disposition product through the nonconforming system.
- Support periodic review activities related to Quality Operations.
- Backup support for finished good release trace activities.
- Support quality improvement related projects
- Demonstrate independent understanding and application of core GMP fundamentals, including but not limited to: Data Integrity (DI), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDPs).
· 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
We are searching for the best talent for Quality Operations Technician.
What you need
EXPERIENCE AND EDUCATION*
· High School Education or GED is required.
· Minimum of two (2) years of experience is required.
SECTION 4: REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS*
- Professional certifications (CQAI, CQA or others) are desired.
- Green Belt Certification preferred.
- Project deployement experience is a plus.
- Previous experience in non-conformance investigations and root cause analysis desired.
- Attention to detail and robust documentation practices are required.
- Must be able to communicate training procedures, specifications, and procedures
- Must be able to work both independently and within cross-functional groups.
- Proficiency in ETQ, JDE, MES, MS Word and Excel is desired.
- Computer experience utilizing such programs as JDE, MS Word and MS Excel, Minitab for project initiatives and problem solving.
- Ability to interpret a variety of instructions furnished in written, oral diagram, or schedule form.
- Medical Device manufacturing experience is preferred.
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, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.
Preferred Skillsnice to have
Good Document Practice (GDP), Quality Operations
Where you'll work
Irving, TXOn-siteOpen in Maps (opens in a new tab)
More jobs in Irving, TXWorking conditions
Job Function
Quality
Job Sub Function
Quality Control
Job Category
Business Enablement/Support
All Job Posting Locations
Irving, Texas, United States of America
From the posting
About Johnson & Johnson
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
Purpose: Responsible for conducting technical quality assurance inspections, quality issue resolution, product containment, and supporting quality improvements for production processes and standards.
Equal opportunity, accessibility and legal noticesJohnson & Johnson's statements, word for word
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 14, 2026
Salary intelligence
How the pay compares
Associate & Specialist roles in Texas5 roles publishing pay
Associate & Specialist roles in the US105 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| Texas (middle half) | $73,000 | $73,000 | $78,500 |
| All US (middle half) | $67,500 | $80,000 | $99,000 |
Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 14, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 574 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 37 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs6
- Investigations and CAPA5
- Data and digital systems4
- Collaboration and leadership4
- GMP and compliance3
- Lab testing and methods1
- Quality systems and risk1
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.
Company hiring pulse
Johnson & Johnson on Regulatory Jobs
- 36
- Open roles
- 36
- Distinct roles
- 15
- Locations
By discipline
- Quality24 67%
- Regulatory7 19%
- Compliance & Safety5 14%
By level
- Senior & Principal11 31%
- Manager9 25%
- Director8 22%
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Quality Operations Technician at Johnson & Johnson
Applications close October 21.