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Job Function:
QualityJob Sub Function:
Quality SystemsJob Category:
ProfessionalAll Job Posting Locations:
Beerse, Antwerp, Belgium, Cork, Cork, Ireland, Fuji, Shizuoka-Ken, Japan, Geel, Antwerp, Belgium, Ghent, East Flanders, Belgium, Latina, Italy, Leiden, Netherlands, Raritan, New Jersey, United States of America, Schaffhausen, Switzerland, Wilson, North Carolina, United States of America, Xian, Shaanxi, ChinaJob Description:
The IM Computer System Validation (CSV) Quality Lead is responsible for assessing, implementing, and continuously improving the IM strategy for computer system validation and the use of embedded AI technology supporting GxP-regulated activities. This role ensures oversight that all IM systems are validated and maintained in a validated state and are NOT using prohibited AI technology throughout their lifecycle, in alignment with global regulatory requirements (e.g., EU GMP Annex 11, FDA 21 CFR Part 11, Annex 22) and J&J quality standards.
The role inventories all IM systems, embedding the collection as an integral of the QMS. It provides direction, oversight, and strategic direction across IM and platforms, ensuring consistent application of risk-based validation approaches, proper AI technology usage, robust data integrity practices (ALCOA+), and lifecycle management of computerized systems.
This position may be based at any of the listed locations or another relevant J&J IM Supply Chain site.
Key Responsibilities:
The Sr. Manager - IM Computer System Validation Quality Lead is accountable and responsible for;
- Acting as IM Quality single point of contact for CSV, ensuring appropriate and timely communication of significant/critical quality and compliance issues linking to Computer System Validation and making recommendations for improvements to relevant senior level stakeholders.
- IM CSV Strategy & Governance
- Onboards and supports the J&J enterprise CSV framework in IM aligned with regulatory expectations and internal quality systems,
- Deploys standards for lifecycle validation, risk-based approaches, and system classification across IM,
- Ensure consistent interpretation and application of Annex 11 requirements across sites,
- Drive harmonization of CSV practices across IM and business units.
- Lifecycle Validation Oversight of all IM GxP-relevant computerized systems
- Validated prior to use,
- Maintained in a validated state throughout their lifecycle,
- Properly retired/decommissioned,
- Oversee validation activities across IM system lifecycle (planning → design → testing → release → maintenance),
- Define and monitor KPIs for validation effectiveness and compliance.
- Data Integrity & Compliance
- Ensure implementation of data integrity principles (ALCOA+) across all systems and processes,
- Ensure compliance with J&J CSV and Data Integrity standards.
- Risk-Based Validation & QRM
- Define and enforce risk-based validation approaches using Quality Risk Management (QRM),
- Ensure appropriate validation effort proportional to system criticality and GxP impact,
- Oversee system risk assessments and mitigation strategies in IM.
- IM System Lifecycle & Technical Compliance
- Guides and oversees System Development Lifecycle (SDLC) / System Lifecycle Management (SLCM) activities (incl. system periodic review activities and follow-ups).
- Supplier & Third-Party Oversight
- Onboards and supports the J&J enterprise process for supplier assessment and CSV deliverables,
- Oversees qualification and monitoring of IM system providers.
- Organizational Leadership & Capability Building
- Lead a global network of CSV leads / site SMEs,
- Provides training for IM CSV roles,
- Provide expert guidance to IM projects, digital initiatives, and innovation programs,
- Promote a culture of compliance, quality, and continuous improvement.
- Continuous Improvement & Innovation
- Supports J&J enterprise teams to drive modernization of validation approaches (e.g., CSA, automation, digitization, AI),
- Identify opportunities to streamline validation while maintaining compliance,
- Align IM CSV strategy with digital transformation initiatives.
- Training
- Develop and deploy fit for purpose CSV training in IM.
The candidate will interface with various stakeholders not limited to Quality Assurance / Quality Systems / IT / Digital & Technology organizations / Manufacturing / QC Analytical Instrument Qualification / Engineering / Data Integrity & Compliance.
Qualifications
- A minimum of University/Bachelor’s degree in Life Sciences, Engineering, Computer Science, or related field. Master’s degree is preferred.
- Extensive experience in CSV within a GxP-regulated environment.
- Proven knowledge of applicable Data Integrity regulations (Annex 11 / 21 CFR Part 11) is required. Working experience within an FDA/EMA GMP (Pharmaceutical) regulated environment is required. Familiarity with ISO requirements.
- Generally requires 10+ combined years of experience in Manufacturing, Quality Assurance, Quality Control, in vaccines/pharmaceutical industry. Solid understanding of the business environment inside a quality organization, across various roles (e.g., quality operations, quality control, quality systems, etc.) is preferred.
- Proven leadership experience in global or cross-site roles.
- Working knowledge of Quality systems such as: Risk Management, Investigation/CAPA, Change Control, Document Management, Management Review process, etc. required.
- Quality mindset and ability to enable Critical & Design Thinking.
- Project Management skills and experiences. Knowledge of Project methodologies and process excellence.
- Strong communication (verbal, written, and presentation) and interpersonal skills, self-awareness and adaptability required.
- Strong facilitation skills and ability to build respectful and productive partnership relationships with peers. Independent thinking. Pragmatism. Ability to zoom-in and out.
- Working experience in navigating and dealing effectively within a matrix organization, managing complexity, engaging and collaborating with multi-disciplined teams across boundaries including remote team members.
- Results oriented with strong track record of success in delivering on objectives. Sense of urgency and ability to zoom-in / zoom out.
Required Skills:
Preferred Skills:
Analytical Reasoning, Analytics Dashboards, Compliance Management, Data Gathering and Analysis, Data Quality, Incident Management, Organizing, Performance Measurement, Quality Control (QC), Quality Management Systems (QMS), Quality Services, Quality Standards, Risk Management, Standard Operating Procedure (SOP), System Integration, Systems Analysis, Tactical Planning, Technical Credibility
The anticipated base pay range for this position is:
€96 000,00 - €165 025,00Benefits:
In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.
*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.
Skills Required
- University or Bachelor's degree in Life Sciences, Engineering, Computer Science, or a related field
- Extensive experience in computer system validation within a GxP-regulated environment
- Knowledge of Data Integrity regulations, including EU GMP Annex 11 and FDA 21 CFR Part 11
- Work experience in an FDA/EMA GMP pharmaceutical-regulated environment
- 10+ combined years of experience in manufacturing, Quality Assurance, or Quality Control within the vaccines or pharmaceutical industry
- Proven leadership experience in global or cross-site roles
- Working knowledge of quality systems, including risk management, investigations/CAPA, change control, document management, and management review
- Project management skills and experience with project methodologies and process excellence
- Strong verbal, written, presentation, facilitation, and interpersonal communication skills
- Experience working effectively in a matrix organization with multidisciplinary and remote teams
- Master's degree
- Familiarity with ISO requirements
Johnson & Johnson Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Johnson & Johnson and has not been reviewed or approved by Johnson & Johnson.
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Healthcare Strength — Healthcare coverage is characterized as comprehensive across medical, dental, and vision, with added supports like onsite clinics, fitness centers, and Employee Assistance resources. Mental-health services and wellbeing reimbursements are also described as meaningful components of the overall package.
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Retirement Support — Retirement offerings are portrayed as a major differentiator, combining a 401(k) with employer matching and an employer-funded pension plan. Stock options and other long-term financial supports are also positioned as part of the broader rewards mix.
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Parental & Family Support — Family-related benefits are presented as notably strong, including paid parental leave for all new parents and additional leave types for caregiving and bereavement. Financial assistance for adoption, fertility treatment, and surrogacy is highlighted as a significant support.
Johnson & Johnson Insights
What We Do
Profound Change Requires Boldness. Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years. The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world. Social Media Community Guidelines: http://www.jnj.com/social-media-community-guidelines







