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Computer System Validation Jobs in Manchester, NH

System Engineer

Raymond, NH · On-site

$71 - $97.90/hr

Qualifications * Bachelor's degree in Electrical Engineering, Computer Science, Software ... Valid driver's license required. Compensation & Benefits The base range for this position in the ...

Partner closely with our US validation partners, some of our most important partnerships. Ensure ... Bachelor's or master's degree in Mechanical Engineering, Computer Science, or related technical ...

Bachelor's degree in Electrical Engineering, Computer Science, Software Engineering, Automation ... Valid driver's license required. #LI-Onsite #LI-KK2 About Symbotic Symbotic is an automation ...

Whatyou'llneed * Bachelor's degree in Electrical Engineering, Computer Science, Software ... Valid driver's licenserequired. #LI-Onsite #LI-KK2 About Symbotic Symbotic is an automation ...

Fully self-reliant networked personal computer user; solid Microsoft Office skills and the ability ... Must Possess of a valid driver's license and/or access to transportation for use in local and ...

Fully self-reliant networked personal computer user; solid Microsoft Office skills and the ability ... Must Possess of a valid driver's license and/or access to transportation for use in local and ...

... department's computer system • Must be able to develop a thorough knowledge of interviewing techniques and personnel matters • Must possess a valid driver's license HOW TO APPLY If you are ...

Showing results 21-40

Computer System Validation information

See Manchester, NH salary details

$10

$52

$83

How much do computer system validation jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for computer system validation in Manchester, NH is $52.98, according to ZipRecruiter salary data. Most workers in this role earn between $40.82 and $62.84 per hour, depending on experience, location, and employer.

What is a computer system validation?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in computer system validation, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in computer system validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It offers opportunities for professionals with skills in validation protocols, regulatory requirements, and tools like GxP and 21 CFR Part 11. The field provides steady employment, career growth, and the chance to work on critical quality assurance processes.

What are the most commonly searched types of Computer System Validation jobs in Manchester, NH?

The most popular types of Computer System Validation jobs in Manchester, NH are:

What are popular job titles related to Computer System Validation jobs in Manchester, NH?

For Computer System Validation jobs in Manchester, NH, the most frequently searched job titles are:

What job categories do people searching Computer System Validation jobs in Manchester, NH look for?

The top searched job categories for Computer System Validation jobs in Manchester, NH are:

Infographic showing various Computer System Validation job openings in Manchester, NH as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, and 5% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $110,196 per year, or $53 per hour.

Verification & Validation Test Engineer

DEKA

Manchester, NH • On-site

Full-time

Re-posted 21 days ago


Job description

DEKA Research & Development, located in Manchester, NH, is seeking a Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a direct impact on the success of our projects. It will be a great opportunity to work on some amazing projects that make a positive impact on the world. Do you want to make a difference with your work? At DEKA you can!
How you will make an impact as a Verification & Validation Test Engineer:
  • Writing test plans, test procedures and other activities involving performance, durability, and reliability assessments
  • Understand device design and core technologies in order to inform test method development
  • Determining test coverage for revisions to design
  • Creating and evaluating test fixtures needed for product design verification
  • Contributing to design failure investigations that may impact Risk Assessment, Hazard Analysis, and FTAs
  • Participating and contributing toward regulatory and agency submissions
  • Authoring Quality Plans, Test Summaries, and other documents

What you need to be successful Verification & Validation Test Engineer:
  • BS in Biomedical, Mechanical, Electrical and/or Robotics/ Automation Engineering
  • 3+ years' experience testing electro-mechanical devices (medical devices preferred)
  • Must have laboratory/ wet lab skills and experience
  • Must have fluid system handling experience
  • Leadership and/or mentoring experience
  • Knowledge and deep understanding of engineering fundamentals
  • Capability to create and clearly explain team objectives and write procedures for others to follow
  • Demonstrated problem solving ability and techniques
  • Ability to work as part of an interdisciplinary team
  • Self-motivated and able to self-prioritize
  • Must have excellent verbal and written communication skills

Preferred skills and experience:
  • Knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience
  • Experience with research, development, and product testing
  • Experience writing procedures for others to follow
  • Experience with data and failure analysis
  • Broad measurement instrument knowledge

About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.