Principal– SAP Computerized System Validation (CSV), Life Sciences- Business Consulting

Infosys Limited; Foster City (CA); On-site; USD 180,000 - 260,000; Full time

Benefits offered by this job

Medical Insurance

401(k) plan

Paid holidays

Job summary

Infosys Limited in Foster City, CA seeks a Principal SAP CSV Lead to drive validation activities for SAP ECC to S/4HANA transformations and implementations. You will define validation strategies, ensure regulatory compliance, and manage deliverables across QA and client teams.

The role requires deep knowledge of GxP, 21 CFR Part 11, GAMP 5, and SDLC validation with Lean/Agile practices. Collaboration with SAP teams across FI/CO, QM, MDG, and data migration is essential.

Qualifications

• Minimum 12+ years of professional Life Sciences experience in a consulting or industry role.
• Experience creating, reviewing and approving validation deliverables.
• Knowledge of risk management and quality requirements for IT projects.

Responsibilities

• Lead CSV activities for SAP ECC to SAP S/4HANA transformation programs and new SAP implementations.
• Develop and execute validation strategies, plans, protocols, and reports for GxP and non-GxP systems.
• Ensure compliance with 21 CFR Part 11, GxP, GAMP 5, and data integrity standards.
• Create, review, approve, and maintain VP, URS, FDS/DS, IQ/OQ/PQ, TRMs, VSRs and SOPs.

Skills

CSV Lead

SAP S/4HANA

GxP Compliance

Regulatory Knowledge

Risk Assessment

SDLC Validation

GAMP 5

Audit Readiness

Data Integrity

SAP S/4HANA Validation

Tools

Solution Manager

SAP GRC

MDG

SNP/ADM

CHARM

HPALM

Job description

Principal– SAP Computerized System Validation (CSV), Life Sciences- Business Consulting

We are looking for people who have demonstrated proven success in roles and through abilities in Computerized System Validation for ERP applications like ECC/SAP S/4 HANA, Cloud Validation, Risk management and Quality Management. The candidate will have to perform validation service activities related to ECC to SAP S/4 HANA transformation or SAP implementation program.

Key Responsibilities

1. Lead Computerized System Validation (CSV) Activities

• Own and drive CSV activities for SAP ECC to SAP S/4HANA transformation programs and new SAP implementations.
• Develop and execute validation strategies, plans, protocols, and reports for GxP and non-GxP systems.
• Ensure validation activities comply with regulatory and company quality requirements.

2. Develop Validation Strategy & Risk-Based Approach

• Define validation frameworks and lifecycle methodologies for SAP S/4HANA programs.
• Conduct system risk assessments and determine validation scope.
• Implement risk-based testing approaches aligned with GAMP 5 and industry best practices.

3. Ensure Regulatory Compliance

• Ensure compliance with 21 CFR Part 11, GxP Regulations, GAMP 5, Data Integrity requirements, Data Privacy regulations, Information Security standards and SOX IT controls.
• Support audit readiness and inspection preparedness.

4. Manage Validation Deliverables

• Create, review, approve, and maintain-Validation Plans (VP), User Requirements Specifications (URS), Functional & Design Specifications, Risk Assessments, IQ/OQ/PQ documents, Traceability Matrices, Validation Summary Reports (VSR) and SOPs and related quality documents.

5. Partner with Quality & Compliance Teams

• Collaborate with client Quality, Compliance, and Validation teams.
• Ensure systems comply with internal policies and health authority requirements.
• Recommend process improvements and updates to CSV procedures and SOPs.

6. Support SAP Implementation Workstreams

• Work closely with SAP functional and technical teams across modules such as: Finance (FI/CO), Supply Chain, Manufacturing, Procurement, Quality Management and Master Data Governance (MDG).
• Assess validation impact of system configuration, enhancements, interfaces, and data migration activities.

Basic Skills & Experience

• Minimum of 12+ years of professional experience in Life Sciences industry working for a consulting services organization and/or industry experience.
• Experience creating, reviewing and approving / acknowledging validation deliverables.
• Knowledge of risk management process and quality management requirements which assures that IT Projects meet Quality and Regulatory requirements.
• Understanding of key pharmaceutical compliance regulations like Computerized System Validation, 21 CFR Part 11, GxP, GAMP 5, SOX IT, Cloud, S4, Data Privacy, Data Integrity and Information Security.
• Develop and document the validation strategy and approach for the Software Development Lifecycle Activities (SDLC) for the global implementation of SAP S4 HANA, considering GxP & Non GxP elements and recommend for risk-based testing approach as required.
• Work with the Client Q&C to ensure system compliance with internal policies, procedures, guidelines, and applicable health authority regulations and provide improvements plan to streamline practices, and revise CSV related SOPs as necessary.
• Work with project management to build an integrated project plan inclusive of the required Computer System Validation (CSV) Lifecycle Deliverables, quality gates and summarization milestones.
• Knowledge on basic function on SAP workstreams/modules.
• Knowledge of various tools/applications used in SAP implementation program Like Solution Manager, CHARM, SAP GRC, DRC, SAP MDG, SAP Rise, Data migration tool (SNP, ADM etc.).
• Successful track record using Lean/Agile approaches to validate assets.
• Proven ability in handling multiple large projects, respond quickly to changing situations in complex environments.
• Ability to pursue and grow deep client relationships.
• Provide leadership in critical engagements and drive successful outcomes.
• Preferable IT background to understand larger impact of architecture / technical complexities on the program.
• Candidates authorized to work for any employer in US without employer-based visa sponsorship are welcome to apply. Infosys is unable to provide immigration sponsorship for this role at this time.

Location: Foster City, California

Required Skills & Experience

• Strong understanding of pharmaceutical compliance regulations and validation concepts.
• Experience of having led large S/4 HANA transformation programs from a Validation Lead perspective.
• Experience with Agile and Waterfall methodologies.
• Familiarity with tools like ServiceNow, JIRA, Veeva, HPALM.
• Ability to manage multiple projects and adapt to complex environments.
• IT background preferred to understand program complexities.
• Excellent communication and collaboration skills.

Benefits

Along with competitive pay, as a full-time Infosys employee you are also eligible for the following benefits:

• Medical/Dental/Vision/Life Insurance
• Long-term/Short-term Disability
• Health and Dependent Care Reimbursement Accounts
• Insurance (Accident, Critical Illness , Hospital Indemnity, Legal)
• 401(k) plan and contributions dependent on salary level
• Paid holidays plus Paid Time Off

About Us

Infosys Consulting is the global management and technology consulting practice of Infosys, a global leader in technology services and consulting. We combine the power of time-tested methodologies, people-driven innovation and disruptive technology to enable leaders of the world’s top brands pursue a path of smart transformation. Together with our clients, internal and external partners, we co-create and execute pragmatic strategies and solutions that transform organizations and define the future of business. Our dynamically growing consultancy offers our consultants:

• Ability to design and implement end-to-end solutions at scale
• A flat organization structure with direct access to our senior-most leaders
• An entrepreneurial environment full of bright, highly motivated consultants
• Opportunities for motivated consultants to impact local communities
• The ability to design your career and drive your professional learning and development
• A truly global culture

EEO

Infosys provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability.