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Computer System Validation Jobs in Pennsylvania (NOW HIRING)

Compli

CSV Lead/ Computer System Validation Lead

Marietta, PA · On-site

$96K - $127K/yr

CSV Lead/ Computer System Validation Lead Location : Marietta, PA Compli, LLC was founded in 2001 to provide Commissioning, Validation and Regulatory Support Services to the Life Sciences industry.

Ztek Consulting

Lab System Validation

West Point, PA · On-site

o Experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. o Experience of CSV Validation in any one of the Lab systems is must. o Should worked in ...

Valspec

Equipment Validation Engineer

Royersford, PA · On-site

The ideal candidate has experience leading the equipment CQV efforts of a team that also includes computer system validation engineers and specialists. Key Responsibilities: * Lead and execute CQV ...

Novocure

Digital Systems Validation Lead

Wayne, PA · On-site

$116K - $130K/yr

Master's degree preferred * 8+ years of experience in computer system validation within regulated industries such as healthcare, pharmaceutical, medical device, or life sciences * Strong knowledge of ...

Novocure

Digital Systems Validation Lead

Wayne, PA · Hybrid

$116K - $130K/yr

Master's degree preferred * 8+ years of experience in computer system validation within regulated industries such as healthcare, pharmaceutical, medical device, or life sciences * Strong knowledge of ...

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How much do computer system validation jobs pay per hour?

As of Jun 24, 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 is the salary of computer system validation?

The salary for a Computer System Validation specialist typically ranges from $70,000 to $120,000 annually, depending on experience, location, and industry. Certifications such as GAMP or CSV training can influence earning potential, and roles often require knowledge of regulatory standards like FDA or ISO.

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 compliance with regulations such as FDA or GMP.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It often requires knowledge of regulatory guidelines, validation protocols, and tools like GxP and 21 CFR Part 11. The field offers steady demand, opportunities for certification, and roles in quality assurance and compliance management.

Is CSV a skill?

In the context of Computer System Validation, CSV refers to Computer System Validation itself, which is a process rather than a skill. However, skills related to CSV include understanding validation protocols, regulatory requirements, and proficiency with validation tools and documentation. These skills are essential for professionals performing CSV tasks in regulated industries like pharmaceuticals and biotech.
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Computer System Validation jobs near you
CSV Lead - Computer System Validation

CSV Lead - Computer System Validation

Centstone

Lancaster, PA • On-site

Full-time

Posted 12 days ago

Job description

Job Title: CSV Lead – Computer System Validation
Location: Lancaster, PA
Experience: 1O–20 Years
Job Type: Long-Term Contract
Work Model: Onsite

Job Summary:
Seeking an experienced CSV Lead to support Computer System Validation activities for a newly constructed Sterile Drug Product Clinical Manufacturing facility. The role involves leading CSV strategy, validation documentation, and execution activities in a GMP-regulated pharmaceutical environment.

Key Skills:

  • Computer System Validation (CSV)

  • AVEVA System Platform & PI Historian

  • Allen Bradley & Siemens PLC

  • SCADA, HMI, OIT Platforms

  • Operational Technology (OT)

  • Instrumentation & Control Systems

  • Alarm Management Systems

  • Robotic Isolators & Lyophilization

  • Autoclave & Equipment Wash Systems

  • Kneat Experience Preferred

Requirements:

  • 10–20 years of CSV experience in Pharma/Biotech

  • Strong GMP/GxP validation knowledge

  • Ability to work independently in fast-paced project environment

  • Excellent communication and deviation management skills

Thanks 

Adarsh Mallik

CENTSTONE LLC

adarsh.mallik@centstone.com

Centstone logo

About Centstone

Sourced by ZipRecruiter

In the dynamic landscape of today’s business environment, flexibility is key. At Centstone, we understand the unique demands of your industry and offer tailored Contract Hiring solutions to empower your organization with the right talent when you need it most.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Hazlet, NJ, US

Year founded

2022

Social media

Facebook

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