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Computer System Validation Jobs in Collegeville, PA

GSK

Senior Validation Engineer

King Of Prussia, PA · On-site

Development of procedures, practices, and policies related to computer system validation. Monitor and update the Validation Master Plan to ensure that it complies with appropriate regulatory ...

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Computer System Validation information

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$10

$53

$85

How much do computer system validation jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for computer system validation in Collegeville, PA is $53.80, according to ZipRecruiter salary data. Most workers in this role earn between $41.44 and $63.80 per hour, depending on experience, location, and employer.

What is a computer system validation?

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 computer system validation, 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 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.

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 offers opportunities for professionals with skills in validation protocols, regulatory requirements, and tools like GxP and 21 CFR Part 11. The field provides steady employment, career growth, and the chance to work on critical quality assurance processes.

What are popular job titles related to Computer System Validation jobs in Collegeville, PA?

For Computer System Validation jobs in Collegeville, PA, the most frequently searched job titles are:

What cities near Collegeville, PA are hiring for Computer System Validation jobs?

Cities near Collegeville, PA with the most Computer System Validation job openings:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in Collegeville, PA as of August 2026, with employment types broken down into 70% Full Time, 6% Part Time, and 24% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $111,900 per year, or $53.8 per hour.

Senior Clinical Computer System Validation Engineer

ICON

Blue Bell, PA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.

Job description

Senior Clinical Computer System Validation Engineer
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are seeking an experienced CSV Quality Consultant to support a strategic software integration program within a regulated pharmaceutical environment.
The consultant will provide quality and validation expertise throughout the lifecycle of computerized systems, ensuring compliance with GxP requirements, data integrity principles, and company quality standards.
What You Will Do:
You will take ownership of software development and engineering deliverables, applying your expertise to complex challenges.
Key responsibilities include:
  • Support the validation lifecycle of computerized systems in accordance with GAMP 5, CSA, and internal quality procedures.
  • Provide quality oversight for software implementation, integration, and data migration activities.
  • Develop and review validation deliverables, validation plans, risk assessments, requirements traceability matrices, test protocols, summary reports, and change controls.
  • Ensure migration and integration activities maintain data integrity, traceability, and regulatory compliance.
  • Partner with business, IT, data, and quality stakeholders to support project delivery and inspection readiness.
  • Review vendor documentation and assess supplier validation approaches.
  • Lead or support computerized system retirement and decommissioning activities, including archival, data retention, and preservation of validation evidence.
  • Identify compliance risks and recommend pragmatic, risk-based solutions.

Your Profile:
  • Bachelor's degree in Life Sciences, Computer Science, Engineering, Information Technology, or a related discipline.
  • Minimum 10 years of experience in Computerized System Validation (CSV) within the pharmaceutical, biotechnology, or medical device industry.
  • Strong knowledge of GxP, GAMP 5, CSA, 21 CFR Part 11, Annex 11, and data integrity principles (ALCOA+).
  • Proven experience supporting system implementations, integrations, and data migration projects.
  • Experience with system decommissioning, archival, and record retention requirements.
  • Excellent stakeholder management, communication, and problem-solving skills.
  • Demonstrated ability to work in cross-functional and global project teams.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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