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Computer System Validation Manager Jobs in Pennsylvania

The Secant Group

Validation Specialist II

Telford, PA

... Management System. This involves writing, reviewing, approving and executing software validation ... Minimum bachelor's degree in science or engineering. BS in a software or computer related degree ...

New

Innovcentric LLC

CSV Lead

King Of Prussia, PA · On-site

$65/hr

King of Prussia, PA Mode (TP/FTE) TP Mandatory Skills Computer System Validation, Computed system assurance, GAMP,GxP risk assessments,Change Management JD 12+ years' Experience in Validating systems ...

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Computer System Validation Manager information

See Pennsylvania salary details

$47.6K

$105.7K

$160.9K

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

As of Jun 24, 2026, the average yearly pay for computer system validation manager in Pennsylvania is $105,668.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,700.00 and $132,300.00 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.

What are the most commonly searched types of Computer System Validation jobs in Pennsylvania? The most popular types of Computer System Validation jobs in Pennsylvania are:
What are popular job titles related to Computer System Validation Manager jobs in Pennsylvania? For Computer System Validation Manager jobs in Pennsylvania, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Manager jobs in Pennsylvania look for? The top searched job categories for Computer System Validation Manager jobs in Pennsylvania are:
What cities in Pennsylvania are hiring for Computer System Validation Manager jobs? Cities in Pennsylvania 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 Pennsylvania as of June 2026, with employment types broken down into 2% Locum Tenens, 5% As Needed, 69% Full Time, 9% Part Time, 12% Contract, and 3% Nights. Highlights an 89% Physical, 5% Hybrid, and 6% Remote job distribution, with an average salary of $105,668 per year, or $50.8 per hour.
Automation Validation Engineer

Automation Validation Engineer

JSat Automation

Blue Bell, PA • On-site

Full-time

Posted 5 days ago

Job description


JSat Automation is hiring an Automation Validation Engineer for their Blue Bell Office. This position is up cowith up to 40% travel to client sites.
This Engineer will be responsible for the following
  • Design and develop manufacturing control systems in support of process operations.
  • Interact with client personnel to identify and analyze continuous improvement through automation upgrades.
  • Develop validation documents per FDA cGMP and GAMP standards, functional specifications, design specifications and requirements trace matrices.
  • Design, program, test and validate process control automation systems.
  • Prepare and execute validation protocols (AIQ, IQ, OQ) for 21 CFR Part 11 compliance per FDA requirements
  • Manage, document, and implement these upgrades through changes control procedures.
  • Execute capital projects including but not limited to:
  • Control system software development
  • Control system hardware design
  • Network design
  • MES system implementation
  • Recipe management
  • User requirement specification development
  • Process equipment installations.
  • SOP development and training on Automation Systems.
  • Troubleshoot, analyze, and resolve field control system issues.
  • Develop, review, and / or execute automation qualification and validation protocols.
  • Design, develop, and implement technical solutions by establishing integration strategies, configuring and programming PLCs, DCSs as well as design, build, install and integrate automation control system hardware, panels and field devices.
  • Up to 40% travel to client sites

Requirements
  • We require a minimum BS Degree in Engineering (Computer Science, Electronics, Electrical, Chemical, etc.) or equivalent with 0 to 7 months experience in process industry.
  • Experience in Control Systems (Emerson DeltaV, Allen Bradley, Foxboro, Siemens, Honeywell). Experience with SCADA, MES, and database systems, or computer system validation are considered a plus.

Apply