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Computer System Validation Manager Jobs (NOW HIRING)

Synectics Inc

Validation Engineer

Devens, MA · On-site

$41.71 - $52.90/hr

Can work independently and manage multiple validation activities simultaneously. * QC lab equipment validation experience required * Need both Computer system validation experience and Equipment ...

SOKOL GxP Services

Validation Engineer

Devens, MA · On-site

... computer system validation scripts using ALM or paper-based methods. * Own change controls related to qualification of QC instruments and associated software. * Update the asset management database ...

CAI

Computer Systems Validation Engineer

Rockville, MD · On-site

$75K - $106K/yr

We provide commissioning, qualification, validation, startup, project management, and other ... System & Industry Expertise Support CSV activities across various platforms including MES, DCS ...

SOKOL GxP Services

Validation Engineer

Devens, MA

... computer system validation scripts using ALM or paper-based methods. * Own change controls related to qualification of QC instruments and associated software. * Update the asset management database ...

CAI

Computer Systems Validation Engineer

Indianapolis, IN · On-site

$75K - $106K/yr

We provide commissioning, qualification, validation, startup, project management, and other ... System & Industry Expertise Support CSV activities across various platforms including MES, DCS ...

Micron

System Validation Technician

Boise, ID · On-site

Associate degree (AAS) in Electronics, Computer Science, IT, or a related field (or equivalent ... At least 1 year of experience using ticketing or workflow management tools (e.g., Jira, ServiceNow ...

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Computer System Validation Manager information

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$47.5K

$105.4K

$160.5K

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

As of Jun 25, 2026, the average yearly pay for computer system validation manager in the United States is $105,415.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $132,000.00 per year, depending on experience, location, and employer.

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 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 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.

More about Computer System Validation Manager jobs
What cities are hiring for Computer System Validation Manager jobs? Cities with the most Computer System Validation Manager job openings:
What are the most commonly searched types of Computer System Validation jobs? The most popular types of Computer System Validation jobs are:
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Computer System Validation Manager jobs near you
Infographic showing various Computer System Validation Manager job openings in the United States as of June 2026, with employment types broken down into 96% Full Time, 1% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $105,415 per year, or $50.7 per hour.
Validation Manager

Validation Manager

Thermo Fisher Scientific

Greenville, NC

Full-time

Posted 4 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 402 frontline employees who took The Breakroom Quiz

187th of 520 rated manufacturers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale...

About the Business
Join our Pharma Services Group (PSG)—a global leader providing integrated drug development and manufacturing solutions to pharmaceutical and biotech companies. Our Greenville, North Carolina site specializes in sterile and oral solid dose (OSD) manufacturing.

Discover Impactful Work
The Validation Manager (C&Q) will lead commissioning and qualification activities across the site, ensuring successful execution of capital projects and operational readiness.

A Day in the Life

  • Lead ~6 direct reports and ~25 contractors
  • Manage commissioning & qualification (C&Q) activities
  • Review and approve capital project requests
  • Allocate resources and manage workload across projects
  • Support equipment implementation and startup
  • Mentor team members and develop co-op pipeline
  • Collaborate cross-functionally across site functions

Keys to Success

Education

  • Bachelor’s degree in Engineering, Science, Chemistry, Biology, or related technical discipline

Experience

  • 6+ years of experience in commissioning, qualification, and/or validation within pharmaceutical or regulated manufacturing environments
  • Minimum 3+ years of leadership experience, including managing engineers and/or contractor teams
  • Hands-on experience supporting capital projects, including commissioning and qualification of new equipment and systems in a Steriles Manufacturing facility
  • Experience reviewing and approving technical project plans, validation strategies, and execution approaches
  • Proven ability to manage highly effective teams (FTEs + contractors) and a complex portfolio of concurrent projects
  • Experience collaborating cross-functionally with quality, process engineering, automation, facilities, maintenance, and operations
  • Experience supporting or developing early talent/co-op programs preferred

Knowledge, Skills, Abilities

  • Strong understanding of cGMP’s and C&Q processes
  • Project and resource management skills
  • Strong leadership and organizational capability

Competencies
Leadership, Project Management, Collaboration, Accountability, Operational Excellence

What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

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