Lead, Computer System Validation T&DQ
$94k - $151.8kJohnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at
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:
QualityJob Sub Function:
Customer/Commercial QualityJob Category:
ProfessionalAll Job Posting Locations:
Horsham Pennsylvania United States of America Raritan New Jersey United States of AmericaJob Description:
Technology & Digital Quality (T&DQ) is a comprehensive organization within J&J that focuses on ensuring the highest standards of quality & compliance. It encompasses a Quality Operations division that handles Computer System Validation (CSV) QMS Management and Commercial Quality Shared Services including specialized support for Transportation Operations and Temperature Control. Additionally it includes a Transformation Office dedicated to steering strategic imperatives and enhancing the Quality & Compliance organizations strategy through initiatives like Data Strategy Automated Product Release and Digitalization of Quality Management Systems. The group further comprises a Data & Digital Strategy function tasked with developing and executing a holistic digital and data strategy to improve quality and compliance covering areas such as Data Foundations AI/ML & IoT technologies Quality & Compliance Innovation and Digital Assets validation. To facilitate the deployment of these strategic initiatives the group employs two Deployment Offices for the MedTech and MedTech segments and maintains a global presence through three regional leaders managing operations in Asia Pacific (ASPAC) Europe Middle East Africa (EMEA) and the Americas.
Within Technology & Digital Quality the IM Deployment office drives targeted strategic transformation and quality operations (CSV) initiatives aligned with the Innovative Medicine (IM) segment strategic priorities.
The Lead Complaints / Adverse Events is responsible for guiding and managing the team throughout the building and execution of quality into enterprise wide systems tools services and infrastructure through the end-to-end lifecycle (design develop implement maintain retire).
- Ensure that all J&J quality standards and global regulatory requirements are met
- Ensure building and execution activities involve early quality involvement in design and development integrating quality into work products implementing controls within applications/solutions and leveraging automation when feasible
- Own the quality approach for systems and hold teams accountable for delivering an end-to-end support model
- Provide technical and procedural expertise/guidance to project teams aligning with internal and external stakeholders
- Plan allocate tasks and resources execute coordinate and maintain validation activities for GxP systems/applications
- Support internal audits and Health Authority regulatory inspections
- Approve SDLC validation documentation deliverables including release of system implementations/changes for production
- Attend project team meetings offering T&DQ quality and compliance guidance and support
- Collaborate with globally diverse teams in an inclusive environment
- Promote an environment fostering the companys credo and the value of a diverse workforce
- Serve as a trusted partner across the Technology & Digital Quality organization fostering strong collaboration skills at the project team level internally and externally
Major Duties /Approximate Percentage of Time
Tasks/Duties/Responsibilities
70% - Building and Execution of Quality into Infrastructure
- Ensures/promotes early involvement of T&DQ in the design and development of applications and infrastructure to ensure automated and preventive controls are built in
- Owns and manages the end-to-end quality process and strategies for building and execution of applications and supporting infrastructure
- Ensures that all Quality Operations related projects go through the Intake process
- Provides strategic direction and operational support to the individual project teams
- Contributes to the creation of strategies for the qualification and validation of new and emerging technologies
- Provides compliance guidance and support to the project teams to ensure successful delivery of the project end-to-end
- Ensures a high degree of inspection readiness in support of health authority inspections audits (internal and external) and periodic review of applications and infrastructure in scope of the T&DQ portfolio
- Participates in audits approves audit non-conformity action plans and approves closure of internal audit findings
- Assists with incident management/CAPA and NC for the systems supported
- Manages the execution of technology quality tasks according to the project plan goals and timelines
- Supports the allocation of resources by accurately communicating availability
- Responsible for managing resources (both internal and external) and ensuring availability for ongoing and upcoming initiatives/projects
- Reviews and approves validation deliverables such as but not limited to Compliance Plans User Requirements/User Stories System Tests User Acceptance Tests Traceability Matrices and Compliance Reports including final release and approval for production use
- Proactively monitors systems and processes to ensure compliance with standard operating procedures and industry best practices
- Works with manager in developing monitoring and managing project costs schedules resources and quality of work product
- Assists or drives status meetings to communicate and address project risks or issues
- Works collaboratively with project teams to keep them informed of project status including any barriers
20% - Stakeholder Management
- Partners with project teams to assess and implement compliant solutions to meet their business needs
- Builds and maintains trusting collaborative relationships and partnerships with internal and external stakeholders which help accomplish key business objectives and helps others to do the same
- Provides partnership insight and direction to cross-functional business leaders and stakeholders regarding T&DQ policies solutions and initiatives
- Communicates proactively with stakeholders to set expectations on the feasibility and timeframe for the delivery of solutions and highlight the risk when quality standards are not met
10%- People Management
- Provides quality guidance and support to project and/or base business support teams
- Utilizes expert knowledge regarding risk management practices and leads and mentors the team with critical thinking and risk-based approaches to carry out validation of computerized systems and infrastructure
- Responsible for the management of consultants and outside service providers assigned to support T&DQ in project teams
- Works with T&DQ leadership to nurture future leaders and create opportunities to grow
- Mentors talent and helps them grow in their careers
Performs other work-related duties as assigned
100% Total
Other Duties:
Develop and maintain an effective working partnership with senior management
Collaborate with other leaders and staff within IM Deployment Office and Quality Operations group to ensure each function is executed in an efficient manner
Ensure timely reports of status and metrics as required by the IM Deployment Office organization
Ensure timely completion of assigned training and expense reports
Required Knowledge Skills and Abilities :
Leadership Competencies
- Demonstrated leadership capabilities fostering diversity and inclusion
- Strong skills in interdependent partnering and influencing
- Experience managing and leading global technology programs along with FTEs/consultant teams across multiple geographies
- Ability to facilitate and communicate key messages and presentations to various cross-functional groups to gain support
- Influence upwards and peers to ensure compliance and regulatory requirements are met
- Make the complex clear and easily understood by others
- Must have the ability to make decisions by seeking out and maintaining trusting and collaborative relationships to meet business needs and demands
Professional Competencies
- Superior written and oral communication skills
- Must have the ability to perform work with a high degree of independence in terms of self-management of a large variety of tasks and initiatives regarding quality and validation
- Solutions oriented striving for new ways to accomplish goals and pragmatic advising ensuring compliance in a cost-effective and risk-based manner
- Must have the ability to work effectively in a highly matrixed team environment
- Ability to manage multiple and competing projects is required
- Works effectively in a virtual team environment
Core Technical Competencies
- Gives input and ensures adoption for how quality will be designed into and maintained within a technology solution
- Understands data integrity needed throughout the lifecycle of a technology solution
- Understands traditional and emerging methods and theory of quality including but not limited to TQM principles Continuous Improvement Cost of Quality Quality 4.0 and Industry 4.0
- Defines strategy for testing according to the risk assessment
- Experience in Testing Management tools like HPALM and JIRA Xray
- Implements elements of an effective quality management system to the organization and its technology solution
- Aware of cybersecurity and privacy principles and implications for quality and risk management activities
- Applies best practices for security role design and segregation of duties within and across technology solutions
- Understands how to prepare an organization and business stakeholders for audits and inspections
- Able to apply digitization tools and techniques to automate simplify digitize and enhance software development and validation processes
- Understands and applies best practices for architecting effective data solutions and frameworks that enable high quality data
- Knowledge of SDLC Quality Management process and Computerized System Validation/Computerized System Assurance principles
- Thorough knowledge of cGMP regulations related to CSV including 21 CFR Part 11 Part 210 Part 211 and Part 820 is required
- Working knowledge of other Global Regulations like EU Annex 11 SOX HCC Security & Privacy ISO is preferred
- Working knowledge of PMO SDLC GAMP 5 and ITIL frameworks is highly desirable
- Knowledge of Software Quality Assurance and Software Quality Engineering is highly desirable
- Knowledge of the following technologies and methodologies highly desirable: Agile SAFe CI/CD RPA Cloud Storage and Computing IoT Data & Analytics AI Intelligent Automation Blockchain Kubernetes XaaS SaMD.
- Project management and organizational skills are required
Degrees and Years of Experience
- A bachelors degree in computer science Information Systems Business Administration or another related field required. Solid relevant experience may be substituted when appropriate additional certifications a plus
- 6 years of progressive experience in the pharmaceutical/medical device/biotech industry with direct experience in Computerized System Validation activities is required
- Experience in large scale end-to-end Validation programs like LIMS CAPA MES PLM SAP LMS Complaints Handling and Change Control is preferred
- Experience authoring or approving validation protocols non-conformities Change Requests SOPs Validation Plans and Reports is required
- Proficiency using the following tools is highly desirable: JIRA HPALM Xray Jenkins Selenium
- Direct experience working in a software development environment using Agile SAFe CI/CD or similar is desirable
Preferred Qualifications:
Preferred Minimum Education : Bachelors or Equivalent
Preferred Area of Study: Technology-related
Preferred Related Industry Experience: Life Sciences Industry Experience
Preferred Knowledge Skills and Abilities :
Certified Software Quality Engineer (CSQE) Certified Quality Engineer (CQE) Certified Quality Auditor (CQA) Project Management Professional (PMP) or similar.
Required Skills:
Preferred Skills:
The anticipated base pay range for this position is :
$94000.00 - $151800.00Additional Description for Pay Transparency:
Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Companys 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: -- ...Purple Drive Computer System Validation (CSV) Consultant Share Raritan, NJ Overview: Role Descriptions: • Demonstratable experience... ...21 CFR Part 11 implementation in Pharma industries. • Leading the Tech Writer team for preparing the test cases. • Co-...Computer
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