1

Computer System Validation Manager Jobs in Tracy, CA

Clayton NC Position Summary The Grifols Therapeutics Manager of Manufacturing Digital Systems, is ... Strong experience with data integrity principles, computer system validation (CSV), and GxP ...

... manager. Use of at least five of the following: Java, ETL, PeopleSoft, Business Systems Analysis, Software Automation Test Suite, Data Modeling Analysis, Software Architecture, Oracle, DB2, and Agile ...

... manager. Use of at least five of the following: Java, ETL, PeopleSoft, Business Systems Analysis, Software Automation Test Suite, Data Modeling Analysis, Software Architecture, Oracle, DB2, and Agile ...

Lead Control System Engineer

Ripon, CA · On-site

$98K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... management systems, and distributed control environments ... Perform code development, testing, validation, and documentation for automation and control systems.

Lead Control System Engineer

Ripon, CA · Remote

$98K - $120K/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... management systems, and distributed control environments ... Perform code development, testing, validation, and documentation for automation and control systems.

Lead Control System Engineer

Ripon, CA · On-site

$98 - $120/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Perform code development, testing, and validation for automation systems * Coordinate and execute ... Bachelor's degree (4-year) in Electrical Engineering, Mechanical Engineering, Computer Engineering ...

New

Product Validation Engineer

Livermore, CA · Hybrid

  • Medical

  • Retirement

... the Manager of Validation but may also receive direction and guidance from senior engineers. IN THIS ROLE YOU WILL * Utilize program targets, system requirements and various control documents to ...

... the Manager of Validation but may also receive direction and guidance from senior engineers. IN THIS ROLE YOU WILL * Utilize program targets, system requirements and various control documents to ...

Product Validation Engineer

Livermore, CA · On-site

  • Medical

  • Retirement

... the Manager of Validation but may also receive direction and guidance from senior engineers. IN THIS ROLE YOU WILL * Utilize program targets, system requirements and various control documents to ...

Product Validation Engineer

Livermore, CA · On-site

  • Medical

  • Retirement

... the Manager of Validation but may also receive direction and guidance from senior engineers. IN THIS ROLE YOU WILL * Utilize program targets, system requirements and various control documents to ...

Store Assistant Manager

Livermore, CA

$18.25 - $24.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

Store Assistant Manager

Livermore, CA · On-site

$18.25 - $24.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... computer system and POS register system. • Assist Store Manager in the selection and hiring of qualified candidates. • Be flexible and occasionally perform work outside your specific role.

Parts Manager

Livermore, CA

$6 - $12K/mo

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Accurately price parts and accessories using the proper pricing source and keep the computer system ... Valid driver license in the state that you will work and a good driving record. We are an equal ...

Parts Manager

Livermore, CA · On-site

$6 - $12K/mo

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Accurately price parts and accessories using the proper pricing source and keep the computer system ... Valid driver license in the state that you will work and a good driving record. We are an equal ...

Parts Manager

Livermore, CA · On-site

$6 - $12K/mo

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Accurately price parts and accessories using the proper pricing source and keep the computer system ... Valid driver license in the state that you will work and a good driving record. We are an equal ...

Parts Manager

Livermore, CA · On-site

$6 - $12K/mo

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Accurately price parts and accessories using the proper pricing source and keep the computer system ... Valid driver license in the state that you will work and a good driving record. We are an equal ...

Quality System Manager

Dublin, CA · On-site

$132K - $165K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Quality Systems Manager is responsible for developing, implementing, and maintaining the ... Oversee validation activities from quality system's perspective at the SSC level. Do you qualify?

next page

Showing results 1-20

Computer System Validation Manager information

See Tracy, CA salary details

$51.1K

$113.5K

$172.8K

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

As of Aug 19, 2026, the average yearly pay for computer system validation manager in Tracy, CA is $113,478.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,200.00 and $142,100.00 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 popular job titles related to Computer System Validation Manager jobs in Tracy, CA?

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

What job categories do people searching Computer System Validation Manager jobs in Tracy, CA look for?

The top searched job categories for Computer System Validation Manager jobs in Tracy, CA are:

What cities near Tracy, CA are hiring for Computer System Validation Manager jobs?

Cities near Tracy, CA with the most Computer System Validation Manager job openings:

Infographic showing various Computer System Validation Manager job openings in Tracy, CA as of August 2026, with employment types broken down into 77% Full Time, 6% Part Time, and 17% Contract. Highlights an 83% In-person, 6% Hybrid, and 11% Remote job distribution, with an average salary of $113,478 per year, or $54.6 per hour.

Sr. Quality Associate II/III, QC, Quality Computer System Validation

Grifols

Clayton, CA

Full-time

Re-posted 7 days ago


Grifols rating

6.5

Company rating: 6.5 out of 10

Based on 277 frontline employees who took The Breakroom Quiz

78th of 86 rated pharmaceutical


Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Schedule: First Shift

Sr. Quality Associate I/II:

Position Summary:

This role is responsible for the implementation, maintenance, and continuous improvement of the Laboratory Information Management System (LIMS) used within the Grifols Therapeutics Quality Control (QC) department, referred to internally as the Laboratory Electronic System (LES). The LES supports the transition toward a fully paperless laboratory by electronically capturing all elements of the QC testing process across multiple highcomplexity assays.

Key Responsibilities:

  • Lead the design, configuration, and ongoing management of the LES, including defining required data elements and establishing appropriate input parameters.
  • Oversee validation activities associated with system updates, enhancements, and change implementations.
  • Serve as a member of the QC computer validation team, ensuring compliance with regulatory and internal validation standards.
  • Support additional computerized systems within the QC environment, including software validation oversight and custom field configuration.
  • Act as a technical resource for troubleshooting and resolving issues related to electronic laboratory systems.
  • Manage and document change controls related to software and system modifications.

Qualifications:

  • Experience with electronic laboratory systems and computerized system validation.
  • Working knowledge of QC laboratory test methods and workflows.
  • Demonstrated experience with change control processes and software/computer validation activities.
  • Strong analytical, documentation, and problemsolving skills.

Education and Experience Requirements by Level:

Quality Associate III,  QC   -  BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 3 yrs of relevant experience or an equivalent combination of education and experience.  Experience managing, projects, teams, etc. is recommended

Sr. Quality Associate I,  QC -   BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 5 yrs of relevant experience or an equivalent combination of education and experience.  Experience managing, projects, teams, etc. is recommended

Sr. Quality Associate II,  QC   - BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 6 yrs of relevant experience or an equivalent combination of education and experience.  Experience managing, projects, teams, etc. is recommended.

Equivalency: Depending on the area of assignment, directly related experience-or a combination of related education, experience, and competencies-may be considered in place of the stated requirements. For example, if a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

Third Party Agency and Recruiter Notice:

Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

Grifols 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.  We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton 

Learn more about Grifols


What Grifols employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Grifols logo

About Grifols

Sourced by ZipRecruiter

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Los Angeles, CA, US

Year founded

2013