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Computer System Validation Remote Jobs in Newtown, PA

Deloitte

System Test and Validation Lead

Princeton, NJ · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... This compensation range is specific to a remote role and takes into account the wide range of ...

Deloitte

System Test and Validation Lead

Princeton, NJ · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... This compensation range is specific to a remote role and takes into account the wide range of ...

Deloitte

System Test and Validation Lead

Princeton, NJ · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent ... This compensation range is specific to a remote role and takes into account the wide range of ...

CEI

Workday HRIS Specialist

Philadelphia, PA · Remote

$38/hr

Remote We are seeking a Workday HRIS Specialist to join the HR Systems & Technology team. This ... Perform system audits, data validations, and data integrity reviews. * Support Workday releases ...

Ivy Rehab Network

HRIS Analyst

Philadelphia, PA · On-site +1

Develop and validate reports, dashboards, audits, and data quality reviews that support operations ... Bachelor's degree in Human Resources, Information Systems, Business Administration, Computer ...

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Computer System Validation Remote information

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How much do computer system validation remote jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for computer system validation remote in Newtown, PA is $50.84, according to ZipRecruiter salary data. Most workers in this role earn between $39.13 and $60.29 per hour, depending on experience, location, and employer.

What is computer system validation (CSV) in a remote job context?

Computer system validation (CSV) is a process used to ensure that IT systems and software used in regulated industries (such as pharmaceuticals or healthcare) work as intended and comply with relevant regulations. In a remote job context, CSV professionals perform validation tasks, documentation, and system testing from an offsite location, often collaborating with teams via digital tools. This remote work typically involves reviewing validation protocols, writing reports, and ensuring compliance with standards like FDA 21 CFR Part 11, all while leveraging secure online platforms to communicate and manage documentation.

What are the key skills and qualifications needed to thrive as a computer system validation (CSV) professional working remotely?

To excel as a Computer System Validation Remote professional, you need a solid understanding of regulatory compliance (such as FDA 21 CFR Part 11), risk management, and validation lifecycle processes, often supported by a degree in computer science, engineering, or a related field. Familiarity with validation software, quality management systems (QMS), and documentation tools is typically required, along with certifications like GAMP or Six Sigma being advantageous. Strong attention to detail, analytical thinking, and effective remote communication are crucial soft skills for this role. These competencies ensure validated systems meet compliance standards, minimize risks, and support seamless collaboration in a regulated, distributed environment.

What are some common challenges faced by computer system validation professionals working remotely, and how can they be addressed?

Remote Computer System Validation (CSV) professionals often encounter challenges such as coordinating validation activities across distributed teams and ensuring secure access to sensitive documentation. Effective communication and use of collaborative tools are crucial for managing documentation reviews, test execution, and issue resolution. Establishing clear validation protocols and regular virtual check-ins with cross-functional teams can help maintain compliance and project momentum. Additionally, leveraging secure cloud-based validation platforms can streamline approvals and maintain data integrity while working remotely.

What is the difference between Computer System Validation Remote vs Computer System Validation on-site?

AspectComputer System Validation RemoteComputer System Validation on-site
Work EnvironmentPerforms validation tasks remotely, often from home or a different location from the client site.Works directly at the client or company site, conducting validation activities in person.
Required CredentialsTypically requires certifications like GxP, 21 CFR Part 11, and validation experience, applicable in both settings.Same certifications as remote roles, with additional familiarity with on-site equipment and facilities.
Industry UsageCommon in industries like pharmaceuticals and biotech where remote oversight is feasible.Traditional in regulated industries requiring on-site validation activities.

Both roles require similar certifications and industry knowledge, but the main difference lies in the work environment—remote versus on-site. Remote validation offers flexibility, while on-site validation involves direct interaction at the facility.

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

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

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

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

Computer System Validation Remote jobs near you
Infographic showing various Computer System Validation Remote job openings in Newtown, PA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $105,757 per year, or $50.8 per hour.

Senior Clinical Computer System Validation Engineer

Blue Bell, PA • On-site, Remote

ICON
See more jobs at ICONexternal

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired 3 days ago. 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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