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Computer System Validation Manager Jobs in Springfield, MA

Cadence Inc

Validation Engineer II

Suffield, CT · On-site

$83K - $105K/yr

Conduct risk assessments and manage change controls. * Ensure regulatory compliance. (GMP, GLP, CSV ... Monitor system performance and lead requalification activities. * Qualify suppliers and vendors.

Dead River Company

Service Dispatcher

Northampton, MA · On-site

$24 - $37/hr

Information is received, input into the computer system, and service scheduled. * Schedules technicians for routine tune-ups and maintenance work as time allows. Service manager may be consulted to ...

Dead River Company

Service Dispatcher

Northampton, MA

$24 - $37/hr

Information is received, input into the computer system, and service scheduled. * Schedules technicians for routine tune-ups and maintenance work as time allows. Service manager may be consulted to ...

Dead River Company

Service Dispatcher

Northampton, MA

$24 - $37/hr

Information is received, input into the computer system, and service scheduled. * Schedules technicians for routine tune-ups and maintenance work as time allows. Service manager may be consulted to ...

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All JobsComputer System Validation JobsComputer System Validation Manager JobsComputer System Validation Manager Jobs in Springfield, MA

Computer System Validation Manager information

See Springfield, MA salary details

$47.3K

$105K

$159.9K

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

As of Jul 15, 2026, the average yearly pay for computer system validation manager in Springfield, MA is $105,046.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,200.00 and $131,500.00 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.

What are the most commonly searched types of Computer System Validation jobs in Springfield, MA? The most popular types of Computer System Validation jobs in Springfield, MA are:
What are popular job titles related to Computer System Validation Manager jobs in Springfield, MA? For Computer System Validation Manager jobs in Springfield, MA, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Manager jobs in Springfield, MA look for? The top searched job categories for Computer System Validation Manager jobs in Springfield, MA are:
What cities near Springfield, MA are hiring for Computer System Validation Manager jobs? Cities near Springfield, MA 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 Springfield, MA as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 82% Physical, 1% Hybrid, and 17% Remote job distribution, with an average salary of $105,046 per year, or $50.5 per hour.

Validation Engineer

Stark Pharma Solutions Inc

Springfield, MA • On-site

Contractor

Posted 20 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Validation Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Validation Engineer
Location: Massachusetts
Duration: Long Term

Position Overview

We are seeking an experienced Validation Engineer to support qualification and validation activities within a pharmaceutical manufacturing environment. This role will focus on equipment qualification, process validation, cleaning validation, computerized system validation, documentation review, and compliance with FDA and cGMP requirements. The ideal candidate will work closely with Manufacturing, Engineering, Quality Assurance, and Regulatory teams to ensure validated systems remain compliant and inspection-ready.

Key Responsibilities

• Develop, execute, and review validation protocols and reports, including IQ, OQ, PQ, and requalification activities.
• Support equipment, utility, facility, process, and cleaning validation programs.
• Prepare and maintain validation documentation in accordance with cGMP and regulatory requirements.
• Coordinate validation activities with Manufacturing, Engineering, Quality Assurance, and project teams.
• Perform risk assessments and gap analyses to identify validation and compliance requirements.
• Investigate validation deviations, implement corrective actions, and support CAPA activities.
• Ensure validation lifecycle activities comply with FDA regulations, 21 CFR Part 210/211, and industry standards.
• Support commissioning and qualification activities for new equipment, facilities, and manufacturing processes.
• Participate in audits, inspections, and validation-related regulatory submissions.
• Contribute to continuous improvement initiatives to enhance validation processes and compliance.

Required Qualifications

• Bachelor's Degree in Engineering, Pharmaceutical Sciences, Biotechnology, Chemistry, Life Sciences, or a related technical discipline.
• 3–7+ years of Validation Engineering experience within pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
• Strong experience with equipment qualification (IQ/OQ/PQ), process validation, and validation lifecycle management.
• Knowledge of cGMP regulations, FDA requirements, data integrity principles, and validation industry standards.
• Experience supporting cleaning validation, computerized system validation (CSV), or utility validation is preferred.
• Familiarity with risk assessments, deviation investigations, CAPA, and change control processes.
• Strong technical writing, documentation, analytical, and problem-solving skills.
• Ability to manage multiple validation projects and work effectively in a cross-functional environment.
• Experience supporting regulatory inspections and audit readiness activities is highly preferred.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/