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Computer System Validation Manager Jobs in Philadelphia, PA

Valspec

CSV Lead

Philadelphia, PA

$103K - $136K/yr

... CSV (Computer System Validation) Lead to support automation and digital systems validation on a major greenfield pharmaceutical manufacturing program. What You'll Do * Manage CSV execution and ...

QED Systems, Inc.

Computer Engineer

Philadelphia, PA · On-site

$112K - $132K/yr

Bachelor of Science Degree in Electrical Engineering or Computer Engineering is required. * 0-5 ... control systems in an industrial environment * Must have a valid US passport or the ability to ...

QED Systems, Inc.

Computer Engineer

Philadelphia, PA · On-site

$112K - $132K/yr

Bachelor of Science Degree in Electrical Engineering or Computer Engineering is required. * 0-5 ... control systems in an industrial environment * Must have a valid US passport or the ability to ...

Johnson & Johnson

Global UDI

West Chester, PA · On-site

Experience with UDI databases, labeling systems, or enterprise data management platforms. * Familiarity with computer system validation (CSV) and digital quality controls. * Experience supporting ...

Jj

Global UDI

West Chester, PA · On-site

Experience with UDI databases, labeling systems, or enterprise data management platforms. * Familiarity with computer system validation (CSV) and digital quality controls. * Experience supporting ...

Pharmaron

Software Validation Senior Associate

Exton, PA · On-site

$75K - $85K/yr

What We're Looking ForBachelor's degree in Computer Science, Engineering, Life Sciences, or a ... Knowledge of software implementation, system upgrades, and change management processes.Computerized ...

CYNET SYSTEMS

Lab Support Engineer

West Point, PA · On-site

$41 - $46/hr

Good knowledge of Computer System Validation. * Good understanding of laboratory instruments and ... Manage end to end lab system lifecycle including implementation, validation, maintenance, and ...

Pharmaron

IT Lab Systems Specialist

Exton, PA · On-site

$75K - $95K/yr

... system implementation, validation, lifecycle management, backup and recovery processes, and ... Computer Science, or a related discipline 5-7 years of IT experience within GMP, GLP, or other ...

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All JobsComputer System Validation JobsComputer System Validation Manager JobsComputer System Validation Manager Jobs in Philadelphia, PA

Computer System Validation Manager information

See Philadelphia, PA salary details

$47.9K

$106.4K

$162K

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

As of Sep 15, 2026, the average yearly pay for computer system validation manager in Philadelphia, PA is $106,373.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,200.00 and $133,200.00 per year, depending on experience, location, and employer.

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 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 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 popular job titles related to Computer System Validation Manager jobs in Philadelphia, PA?

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

What job categories do people searching Computer System Validation Manager jobs in Philadelphia, PA look for?

The top searched job categories for Computer System Validation Manager jobs in Philadelphia, PA are:

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

Cities near Philadelphia, PA 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 Philadelphia, PA as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $106,373 per year, or $51.1 per hour.

Laboratory IT Associate

King Of Prussia, PA • On-site

Prism Biotech
See more jobs at Prism Biotechexternal

Full-time

Re-posted 21 days ago

Job description

This role will serve as a business representative for laboratory IT systems and will be responsible for mentoring laboratory personnel on the use of electronic lab systems as well as supporting internal and external audits as a laboratory IT system subject matter expert.
Key Objectives/Deliverables:
  • Performs or supports Laboratory with the validation of laboratory equipment and software systems.
  • Supports the establishment and maintenance of the validated state of software-based computerized systems in use in the laboratory.
  • Act as business owner and contact SME for QC laboratory IT systems.
  • Responsible for collecting data and authoring periodic review documents for laboratory information systems.
  • Provide oversight and support continuous improvement of quality systems as they relate to laboratory informatics.
  • Apply knowledge of quality principles, cGMP, and laboratory systems towards the development and execution of local procedures, training courses, and practices.
  • Assist in improvement of quality systems by creating or revising worksheets, developing, or updating laboratory execution system documentation, updating laboratory methods, and maintaining other lab documentation systems.
  • Responsible for method management in the QC Laboratory, specific to scripted or coded methods.
  • Supports and/or leads investigations, CAPA and change control initiatives.
  • Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
  • Ability to work in a lab environment including wearing appropriate PPE and other safety related equipment or considerations.
Requirements (Education, Experience, Training):
  • Bachelor’s degree in a computer science, life science, or applied science with at least five (5) years of demonstrated relevant experience in a GMP lab.
Preferred attributes but not required:
  • Experience with computer systems including Microsoft Office suite, laboratory information management systems.
  • Investigation and deviation management experience.
  • Demonstrated proficiency in computer system validation.
  • Experience with compliance requirements and regulatory expectations.
  • Demonstrated accuracy and proficiency in analytical skills.
  • Strong oral and written communication skills and demonstrated through documentation and presentation skills.
  • Demonstrated strong interpersonal interaction skills.

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