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Computer System Validation Jobs in Pennsylvania (NOW HIRING)

$93K - $175K/yr

Write test plans and testing scripts in support of Computer System Validation (CSV) team * Ensure systems meet GxP, FDA 21 CFR Part 11, and other regulatory requirements as required based on ...

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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 ...

Support and execute computerized system validation activities throughout the entire system ... Bachelor's degree in Information Technology, Computer Science, Life Sciences, Engineering, or a ...

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Computer System Validation information

See Pennsylvania salary details

$10

$54

$86

How much do computer system validation jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for computer system validation in Pennsylvania is $54.45, according to ZipRecruiter salary data. Most workers in this role earn between $41.92 and $64.57 per hour, depending on experience, location, and employer.

What are some typical challenges faced in Computer System Validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

What is a Computer System Validation job?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What is the work of computer system validation?

Computer System Validation (CSV) is the process of ensuring that computer systems used in regulated environments function correctly and comply with industry standards. It involves documenting and testing software, hardware, and related processes to verify they meet specified requirements, often using validation protocols and tools. CSV is essential in industries like pharmaceuticals and healthcare to ensure data integrity and regulatory compliance.

What degree is best for cis jobs?

For Computer System Validation (CSV) roles, a bachelor's degree in computer science, information technology, life sciences, or engineering is typically preferred. Relevant certifications such as GxP or validation-specific training can enhance job prospects, and strong knowledge of regulatory requirements like FDA or EMA guidelines is beneficial.

What is the salary of SoC validation engineer?

The salary of a SoC validation engineer typically ranges from $80,000 to $130,000 annually, depending on experience, location, and company size. Professionals in this role often have skills in hardware description languages and verification tools, which can influence compensation.
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:
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What job categories do people searching Computer System Validation jobs in Pennsylvania look for? The top searched job categories for Computer System Validation jobs in Pennsylvania are:
What cities in Pennsylvania are hiring for Computer System Validation jobs? Cities in Pennsylvania with the most Computer System Validation job openings:
Infographic showing various Computer System Validation job openings in Pennsylvania as of July 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 78% Physical, 5% Hybrid, and 17% Remote job distribution, with an average salary of $113,254 per year, or $54.4 per hour.
Automation Validation Engineer

Automation Validation Engineer

JSat Automation

Blue Bell, PA • On-site

Full-time

Re-posted 26 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.