New · posted Oct 25
Johnson & Johnson · Medical Devices
Technology Manager, Quality Systems Analyst
- Raynham, MA
- Hybrid
- 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.
DePuy Synthes is recruiting for a Technology Mgr, Quality Systems, Analyst , located in Raynham, MA or West Chester, PA or New Brunswick, NJ or Palm Beach Gardens, FL or Warsaw, IN.
The Technology Manager, Quality Systems, Analyst leads the technology capability supporting DePuy Synthes enterprise quality systems within the Supply Chain Technology function, Quality sub-function. This role manages a team of individual contributors and/or supervisors and is accountable for effective performance management, capability building, and career development. The Manager develops tactical and operational plans for the quality systems portfolio, owns and executes the product roadmap across complaint handling, CAPA, nonconformance, document management, training, and audit platforms, and prioritizes and maintains the backlog balancing the requirements of Quality, Regulatory, Manufacturing, and Technology stakeholders. Operating in a regulated MedTech environment, the role ensures all platform changes meet GxP, 21 CFR Part 11, and data integrity requirements while driving analytics, automation, and continuous improvement across the quality technology landscape.
What you need
Education
Required: Bachelor's degree in Computer Science, Information Systems, Engineering, Life Sciences, Quality, Industrial Engineering or a related discipline.
Preferred: Master's degree in Information Systems, Engineering, or Business Administration.
Required:
8 years of progressive experience delivering and supporting enterprise quality systems or regulated business applications in a manufacturing or MedTech environment.
Minimum 2 years of experience leading teams, with demonstrated ability to manage performance, develop talent, and deliver results through others.
Deep hands-on experience with enterprise quality management systems (e.g., Veeva Vault QMS, TrackWise, ETQ, Sparta, or equivalent) across complaint, CAPA, nonconformance, and document control processes.
Strong working knowledge of GxP, 21 CFR Part 11, computer system validation, and data integrity (ALCOA+) requirements.
Proven experience owning a product roadmap and backlog for a regulated platform portfolio.
Experience defining quality metrics, analytics, and executive reporting from quality system data.
Experience integrating quality systems with ERP (SAP), PLM, and manufacturing systems.
Experience managing vendors, system integrators, or managed service partners against defined SLAs.
Strong stakeholder management and communication skills, with proven ability to influence Quality and Regulatory leadership.
Preferred:
MedTech or medical device experience; familiarity with ISO 13485, EU MDR, and FDA QSR/QMSR requirements.
Experience leading quality systems migration, consolidation, or stand-up within a divestiture, carve-out, or standalone entity.
Experience applying Generative AI / LLM-enabled tooling to complaint triage, document review, or quality record analysis, with appropriate validation controls.
Familiarity with Agile/Scrum delivery and backlog-driven product management in a regulated context.
Proficiency with reporting and visualization tools (Power BI, Tableau) and SQL for quality analytics.
Exposure to intelligent automation platforms (RPA, workflow automation) applied to quality operations.
Experience supporting regulatory inspections and external audits as a technology representative.
Familiarity with cloud platforms (Azure, AWS) and validated cloud application management.
Other:
Travel: Up to 20% domestic travel expected across DePuy Synthes manufacturing and office sites.
Language: English proficiency required.
Certifications: Lean/Six Sigma, ASQ CQE/CQA, ITIL v4 Foundation, PMP, or relevant quality systems platform certification preferred.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.
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
Analytical Reasoning, Consulting, Cost Management, Developing Others, Human-Computer Interaction (HCI), Inclusive Leadership, Leadership, People Performance Management, Performance Measurement, Product Development, Product Strategies, Project Management Methodology (PMM), Research and Development, Resource Management, Software Development Management, Strategic Supply Chain Management, Team Management
What you'll do
Develops tactical and operational plans to achieve quality systems technology goals, and communicates plans to managers, supervisors, and individual contributors.
Develops, owns, and executes the product roadmap for the enterprise quality systems portfolio, aligning platform capability to Quality and Regulatory strategy.
Prioritizes and maintains the backlog for assigned quality platforms, balancing the requirements of Quality process owners, Regulatory, Manufacturing, and Technology stakeholders.
Leads the product functional design process based on an intimate knowledge of quality system users, regulated processes, and platform technology.
Directs configuration, enhancement, and support of validated quality platforms covering complaint handling, CAPA, nonconformance, deviations, change control, document management, training records, and audit management.
Oversees analytics and reporting capability across quality data — defining metrics, dashboards, and trend analysis that give Quality leadership visibility into record aging, cycle time, and compliance posture.
Ensures all platform changes follow computer system validation, change control, and documentation requirements consistent with GxP, 21 CFR Part 11, and data integrity (ALCOA+) expectations.
Directs integration of quality systems with ERP (SAP), PLM, manufacturing execution, and post-market surveillance systems.
Identifies and delivers automation and AI-enabled improvement opportunities across quality processes, ensuring appropriate validation and human-in-the-loop controls.
Manages vendor and managed service partner relationships, including scope definition, quality of deliverables, and SLA performance.
Serves as the technology point of contact for internal, external, and regulatory audits and inspections, coordinating evidence, validation documentation, and remediation.
Assesses the quality systems implications of technology change — including platform migrations, ERP implementations, and separation/carve-out activity — and defines requirements ahead of cutover.
Anticipates bottlenecks, provides escalation management, and builds consensus by understanding stakeholder requirements and constraints.
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
Pension and 401(k) savings plan
Long-term incentive program
Vacation (120 hours per year)
Sick time (40 hours per year)
13 paid holidays per year
Parental leave (480 hours)
Where you'll work
Raynham, MAHybridOpen in Maps (opens in a new tab)
More jobs in Raynham, MAWorking conditions
Job Function
Technology Product & Platform Management
Job Sub Function
Technical Product Management
Job Category
People Leader
All Job Posting Locations
Raynham, Massachusetts, 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
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.
The following link to general company benefits information MUST also be included in the posting: Please use the following language:
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 26, 2026
Salary intelligence
How the pay compares
This role's midpoint is 9% below the US median for Quality Assurance roles at this level.
This roleEmployer provided
Manager roles in Massachusetts19 roles publishing pay
Manager roles in the US112 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $102,000 | — | $177,100 |
| Massachusetts (middle half) | $117,000 | $137,500 | $153,000 |
| All US (middle half) | $130,875 | $153,000 | $167,625 |
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 26, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 921 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 46 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Quality systems and risk16
- Collaboration and leadership10
- Data and digital systems9
- GMP and compliance7
- Documentation and SOPs7
- Validation and qualification7
- Investigations and CAPA4
- Regulatory submissions2
- Lab testing and methods1
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
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- 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
Company hiring pulse
Johnson & Johnson on Regulatory Jobs
- 36
- Open roles
- 35
- Distinct roles
- 18
- Locations
By discipline
- Quality23 64%
- Regulatory12 33%
- Compliance & Safety1 3%
By level
- Associate & Specialist13 36%
- Senior & Principal12 33%
- Manager7 19%
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Technology Manager, Quality Systems Analyst at Johnson & Johnson
Applications close October 30. $102K–$177K a year, employer provided.