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Computer System Validation Manager Jobs in California

Socket.dev

AMS Validation Manager

San Diego, CA · On-site

$180 - $240/hr

DESCRIPTION We are seeking an experienced, hands-on manager to lead the AMS Silicon Validation team ... robotic test systems, machine learning, and data analytics applied to silicon validation.

Apple

AMS Validation Manager

San Diego, CA · On-site

$225K - $338K/yr

... systems, data analytics, and engineering productivity. - Manage multiple concurrent silicon ... Preferred Qualifications Experience validating advanced mixed-signal or high-speed interfaces, such ...

Apple Inc.

AMS Validation Manager

San Diego, CA · On-site

$226 - $338/hr

... systems, data analytics, and engineering productivity. * - Manage multiple concurrent silicon ... Experience validating advanced mixed‑signal or high‑speed interfaces, such as, SerDes, PCIe ...

CoolPlacesToWork

Ams Validation Manager

San Diego, CA · On-site

$140 - $210/hr

... systems, machine learning, and data analytics applied to silicon validation. • Demonstrated ... management experience leading validation or mixed-signal engineering teams. • Strong hands-on ...

JSat Automation

Validation Engineer

Glendale, CA · On-site

MES system implementation * Recipe management * User requirement specification development ... Experience with SCADA, MES, and database systems, or computer system validation are considered a ...

ARES Corporation

Computer System Analyst

Lompoc, CA · On-site

$130K - $139K/yr

ARES is seeking computer system analyst and IT system engineer / architect candidates to support ... analysis, risk management, data modeling, and others. * Experience with digital engineering ...

Apple

AMS Validation Manager

San Diego, CA · On-site

We are seeking an experienced, hands-on manager to lead the AMS Silicon Validation team in San ... robotic test systems, machine learning, and data analytics applied to silicon validation.

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All JobsComputer System Validation JobsComputer System Validation Manager JobsComputer System Validation Manager Jobs in California

Computer System Validation Manager information

See California salary details

$46.9K

$104K

$158.4K

How much do computer system validation manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for computer system validation manager in California is $104,035.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $130,300.00 per year, depending on experience, location, and employer.

What does a computer system validation manager do?

A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.

What are the key skills and qualifications needed to thrive as a computer system validation manager, and why are they important?

To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.

What are some common challenges a computer system validation manager faces during system implementation projects?

A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.

What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?

AspectComputer System Validation ManagerComputer System Validation Specialist
CertificationsGAMP, CQE, CSQEGAMP, CQE, CSQE
Work EnvironmentManagement, oversight, strategic planningExecution, testing, documentation
Industry UsagePharmaceutical, biotech, regulated industriesPharmaceutical, biotech, regulated industries
Primary FocusLeading validation projects, team coordinationPerforming validation activities, testing

The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.

What are the most commonly searched types of Computer System Validation jobs in California?

The most popular types of Computer System Validation jobs in California are:

What are popular job titles related to Computer System Validation Manager jobs in California?

For Computer System Validation Manager jobs in California, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Manager jobs in California look for?

The top searched job categories for Computer System Validation Manager jobs in California are:

What cities in California are hiring for Computer System Validation Manager jobs?

Cities in California with the most Computer System Validation Manager job openings:

Computer System Validation Manager jobs near you
Infographic showing various Computer System Validation Manager job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $104,035 per year, or $50 per hour.

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

Infosys

Foster City, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Infosys rating

7.0

Company rating: 7.0 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

153rd of 226 rated it services

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 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.
Principal Consultant - SAP S/4HANA Validation Lead (Life Sciences)
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
• Provide leadership in critical engagements and drive successful outcomes
  • 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.
EEO/About Us
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.

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