This job posting is anticipated to close on Nov 11 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.
Description
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.
Job Function:
Legal & ComplianceJob Sub Function:
Product SecurityJob Category:
ProfessionalAll Job Posting Locations:
New Brunswick, New Jersey, United States of America, West Chester, Pennsylvania, United States of AmericaJob Description:
Job Overview
The Professional, Quality Steward is an individual contributor within the Product Security organization responsible for providing quality stewardship and oversight of cybersecurity activities across the medical device and connected-product lifecycle.
This role partners with Product Security, R&D, Systems Engineering, Software Engineering, Quality, and Regulatory Affairs to ensure cybersecurity activities are appropriately planned, documented, reviewed, and maintained in accordance with the Quality Management System (QMS), design controls, regulatory requirements, and Product Security processes.
The Quality Steward helps ensure cybersecurity deliverables and objective evidence are complete, consistent, traceable, and inspection-ready, supporting the development and maintenance of safe, secure, and compliant products.
Key Responsibilities
·
- Provide quality and compliance guidance for cybersecurity activities, including security planning, threat modeling, cybersecurity risk assessments, security requirements, testing, SBOMs, and vulnerability management.
- Serve as the Quality Steward for Product Security across assigned products, platforms, and programs throughout the product lifecycle.
- Review Product Security deliverables and objective evidence for completeness, traceability, consistency, and alignment with established QMS and cybersecurity processes.
- Ensure cybersecurity activities are appropriately integrated into design controls, product risk management, Design History Files, and lifecycle processes.
- Partner with Product Security, R&D, Quality, and Regulatory Affairs to identify and resolve cybersecurity documentation, process, and compliance gaps.
- Support cybersecurity content and evidence for regulatory submissions, audits, inspections, and responses to regulatory authorities.
- Provide quality stewardship for postmarket cybersecurity and vulnerability management, including risk assessments, remediation documentation, product changes, and coordinated vulnerability disclosure activities.
- Support governance of SBOMs and third-party/open-source software cybersecurity risk throughout the product lifecycle.
- Assess Product Security quality impacts associated with product changes, software releases, supplier changes, platform migrations, and lifecycle transitions.
- Support development and continuous improvement of Product Security procedures, work instructions, templates, metrics, and training.
- Monitor evolving medical-device cybersecurity regulations and standards and help translate requirements into practical Product Security and Quality System processes.
Qualifications
Education
- Bachelor’s degree in Engineering, Computer Science, Cybersecurity, Information Systems, Quality, Biomedical Engineering, or a related technical discipline.
- Advanced degree preferred.
Required Experience and Skills
- 4+ years of experience in medical-device Quality, software quality, design assurance, product security, cybersecurity compliance, systems engineering, or a related regulated product-development discipline.
- Experience with design controls, risk management, verification and validation, change control, and Quality Management Systems.
- Working knowledge of cybersecurity concepts including threat modeling, cybersecurity risk management, vulnerability management, security testing, and SBOMs.
- Experience reviewing technical documentation and objective evidence for completeness, traceability, and compliance.
- Strong communication and cross-functional collaboration skills.
Preferred
- Medical device, MedTech, digital health, or other regulated-product experience
- Knowledge of FDA medical-device cybersecurity expectations, ISO 14971, ISO 13485, IEC 62304, IEC 81001-5-1, and AAMI TIR57/TIR97.
- Experience reviewing cybersecurity deliverables such as threat models, cybersecurity risk assessments, security requirements, penetration-test reports, SBOMs, and vulnerability assessments.
- Experience supporting regulatory submissions, audits, inspections, or postmarket cybersecurity activities.
- Relevant certifications such as CQE, CSQE, RAC, CSSLP, CISSP, or CISA preferred.
Required Skills:
Preferred Skills:
AI Judgement Integration, Business Behavior, Compliance Management, Critical Thinking, Cybersecurity, Fraud Management, Legal Services, Problem Solving, Process Oriented, Risk Assessments, Security Architecture Design, Security Incident Response, Security Policies, Situational Awareness, Standard Operating Procedure (SOP), Technical Credibility, Technology Quotient, Training Delivery MethodsThe anticipated base pay range for this position is :
$81,000.00 - $131,100.00Additional 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
Additional information can be found through the link below.
Co-Ops and Intern Positions: Please use the following language:
Co-Ops/Interns are eligible to participate in Company sponsored employee medical benefits in accordance with the terms of the plan.
Co-Ops and Interns are eligible for the following sick time benefits: up to 40 hours per calendar year; for employees who reside in the State of Washington, up to 56 hours per calendar year.
Co-Ops and Interns are eligible to participate in the Company’s consolidated retirement plan (pension).
Positions Represented by CBA: Please use the following language:
This position is eligible for benefits to include medical, dental, vision and time off, as well as any others as provided for in the applicable Collective Bargaining Agreement
For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits
