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Computer System Validation Manager Jobs in Texas

Spruce Infotech

Validation Expert

Fort Worth, TX · On-site

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.

Graphcore

Hardware Validation Manager

Austin, TX · On-site

It is developing hardware, software and systems infrastructure that will unlock the next generation ... Job Summary We are seeking an experienced Hardware Validation Manager to lead the validation of ...

Graphcore

Hardware Validation Manager

Austin, TX

It is developing hardware, software and systems infrastructure that will unlock the next generation ... Job Summary We are seeking an experienced Hardware Validation Manager to lead the validation of ...

Inteldot

MES Specialist

San Juan, TX

Exposure to system validation and CSV (Computer System Validation) processes * Familiarity with ISA-95 integration concepts * Strong communication skills and ability to work in cross-functional teams

Inteldot

MES Specialist

San Juan, TX · On-site

Exposure to system validation and CSV (Computer System Validation) processes * Familiarity with ISA-95 integration concepts * Strong communication skills and ability to work in cross-functional teams

Pacer Group

Non-Product Validation Engineer

Plano, TX · On-site

$33/hr

... systems used in our quality management system processes comply with ISO 13485 standards and ... Bachelor's degree in Engineering, Computer Science, or related technical field * Minimum 5 years of ...

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Computer System Validation Manager information

See Texas salary details

$44.3K

$98.2K

$149.5K

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

As of May 30, 2026, the average yearly pay for computer system validation manager in Texas is $98,211.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,400.00 and $123,000.00 per year, depending on experience, location, and employer.

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 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 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.

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Computer System Validation Manager jobs near you

Computer System Validation-Pharmaceutical

PharmEng Technology

Fort Worth, TX • On-site

Other

Posted 26 days ago

Job description

Title: Computer Validation Specialist-PQM Location: Fort Worth, TX Company: PharmEng Technology Inc. PharmEng Technology is a full service consulting firm that serves the pharmaceutical, medical devices and biotechnology industries in North America and internationally. Since 1997, the company has provided industry recognized consulting services assisting clients in the rapid commercialization of new product from drug discovery, strategic planning to process scale up.

PharmEng has immediate opening for candidates with experience in Process Validation Engineer. Essential Functions and Responsibilities Proficient in Validation and Qualification aspects of systems. If required, creates and documents Validation Plan, Quality Plan, IQ Report, OQ Report, and Validation Summary Reports.

Drive continuous improvement of the quality system to meet and sustain compliance with internal and external regulatory requirements Conduct Quality reviews to evaluate if processes and deliverables fulfill the requirements for quality, to uncover errors or deficiencies in processes and deliverables, and to identify strengths and opportunities for improvement Follow up resolution of identified quality exposures and escalation to line management if critical situations are not resolved in due course Contribute to business decisions in the decisions in the definition and assessment of IT requirements Support the development and delivery of training in quality matters Drive and facilitate create of relevant of system SOPs. Prepare and follow internal authority inspections. Prepare, or review and approve major system documentation to ensure consistency with quality standards and quality deliverables.

Coordination documentation, testing and change management activities to ensure compliance with business and regulatory needs Develop PQM resources for projects and services and monitor their performance to ensure adherence with agreed quality systems. Forecast demand and plan for IT PQM related to projects, provide task estimating and ICE roadmap to PMs, monitor and manage project risk and compliance Ownership IT CAPA and CCR Process for the responsible functional areas. Minimum Qualifications: Bachelor's of Science and a minimum of 5 years experience in IT in pharmaceutical industry with expert knowledge of current regulations Ability to interact with all levels of the organization Influence and leadership capability, and credibility within the business Strong organization skills Strong written and verbal communication skills Excellent written and spoken English Thank you for your interest in our organization.

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