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Computer System Validation Manager Jobs in Springfield, MA

Marriott

Operations Supervisor

Windsor, CT · On-site

POSITION SUMMARY Complete designated cashier and closing reports in the computer system. Review ... Report accidents, injuries, and unsafe work conditions to manager; complete safety training and ...

Gallagher Fluid Seals Inc

Warehouse

East Longmeadow, MA · On-site

$19 - $25/hr

Make stock adjustments on company computer system after investigation and communication to manager of large discrepancies. * Perform all other duties assigned Requirements: * Willingness to ...

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Computer System Validation Manager information

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$47.3K

$105K

$159.9K

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

As of Jun 1, 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 May 2026, with employment types broken down into 24% Full Time, 68% Part Time, and 8% Contract. Highlights an 85% Physical, and 15% Remote job distribution, with an average salary of $105,046 per year, or $50.5 per hour.

Senior Computer Systems Validation (CSV) Specialist

Karl Storz GmbH & Co. KG

Charlton, MA

Other

Posted 5 days ago

Job description

Senior Computer Systems Validation (CSV) Specialist

Location: Charlton, MA or Goleta (Santa Barbara), CA

Join a global leader in medical technology and help shape the future of digital quality and compliance. KARL STORZ is a family-owned, innovationdriven organization known for advancing minimally invasive surgery and delivering worldclass endoscopy solutions for more than 80 years. With a strong culture of collaboration, integrity, and continuous improvement, KARL STORZ North America offers the opportunity to make a meaningful impact in healthcare while growing your career in a supportive, peoplefirst environment.

 

About the Role

We are seeking a Senior Computer Systems Validation (CSV) Specialist to lead and manage nondevice software validation activities across our U.S. manufacturing and distribution sites. In this highly visible role, you will collaborate with global teams, ensure compliance with regulatory requirements, and drive bestinclass validation practices that support our Quality Management System and operational excellence.

 

What You'll Do

  • Lead and manage the global CSV process for U.S. sites, partnering with crossfunctional and international teams.
  • Evaluate, audit, and guide software validation activities to ensure compliance with FDA, ISO, and internal standards.
  • Develop, review, and oversee validation lifecycle documentation, including plans, protocols, risk assessments, and reports.
  • Analyze validation data, identify gaps, and support investigations and corrective actions.
  • Manage vendors and consultants providing CSV services.
  • Maintain validation tracking databases and contribute to process improvement initiatives.
  • Represent CSV and IT during audits and regulatory inspections.

 

What You Bring

 

Required:

  • 7+ years of CSV experience, including 5+ years in a regulated industry (medical device, aerospace, automotive, etc.).
  • Associate degree in Applied Science or equivalent experience/certifications.
  • Strong knowledge of ISO 13485, FDA 21 CFR 820, and 21 CFR Part 11.
  • Expertise in software validation standards, technical writing, and documentation control.
  • Experience managing validation projects and collaborating across technical and business teams.
  • Exceptional organizational, communication, and technical writing skills.
  • Ability to manage multiple complex projects independently.
  • Ability to travel up to 10%

 

Preferred:

  • Bachelor's degree in software engineering, computer science, IT, or related field.

 

Why KARL STORZ

  • Work for a respected global medical technology leader with a strong commitment to quality and innovation.
  • Join a collaborative culture that values professional growth, continuous learning, and crossfunctional teamwork.
  • Contribute to solutions that directly support patient care and healthcare advancement.
  • Enjoy competitive benefits, stability, and the opportunity to influence global processes.

 

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