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Computer Validation Jobs in New Hampshire (NOW HIRING)

Lonza

Computer Systems Validation Engineer

Portsmouth, NH · On-site

$85 - $110/hr

Computer Systems Validation Engineer United States, Portsmouth (New Hampshire) Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. The ...

JobRx, Inc.

Director, Validation

Bedford, NH · On-site

$120 - $160/hr

The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...

PCI Pharma Services

Director, Validation

Bedford, NH · On-site

The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...

PCI Pharma Services

Director, Validation

Bedford, NH · On-site

The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...

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All JobsComputer Validation JobsComputer Validation Jobs in New Hampshire

Computer Validation information

See New Hampshire salary details

$10

$52

$83

How much do computer validation jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for computer validation in New Hampshire is $52.83, according to ZipRecruiter salary data. Most workers in this role earn between $40.67 and $62.64 per hour, depending on experience, location, and employer.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

Is computer validation a good field?

Computer validation is a specialized field within quality assurance and regulatory compliance, focusing on ensuring that computerized systems meet industry standards such as 21 CFR Part 11. It often requires knowledge of validation protocols, testing, and documentation, and can offer stable employment opportunities in regulated industries like pharmaceuticals and biotech. The field values certifications and technical skills, making it suitable for professionals interested in compliance, quality systems, and technology validation.

What are popular job titles related to Computer Validation jobs in New Hampshire?

For Computer Validation jobs in New Hampshire, the most frequently searched job titles are:

What job categories do people searching Computer Validation jobs in New Hampshire look for?

The top searched job categories for Computer Validation jobs in New Hampshire are:

Computer Validation jobs near you
Infographic showing various Computer Validation job openings in New Hampshire as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $109,877 per year, or $52.8 per hour.

Computer Systems Validation Specialist

Lonza Group Ltd.

Portsmouth, NH • On-site

$90 - $130/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

Computer Systems Validation (CSV) Specialist Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families.

The Computer Systems Validation (CSV) Specialist helps to lead team members to assess new and changing computer systems to ensure compliance with company policies, procedures and industry guidance.

The CSV Specialist will risk assess systems, review change requests and test scripts, draft protocols and initiate and review GMP documentation revisions. This position also provides guidance to junior team members and will be involved as the QA CSV representative during small and large-scale projects.

What you will get:
  • A collaborative and inclusive work environment.
  • Opportunities for career growth and development.
  • Access to cutting-edge technologies and tools.
  • Competitive compensation and benefits package.
  • Supportive leadership and mentoring.
  • Commitment to ethical and sustainable practices.
  • Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:
  • Perform all aspects of QMS process’ – Change Control, Deviations, CAPAs.
  • Execute all responsibilities as CSV project lead for simple projects.
  • Oversee/perform all CSV qualification activities for DeltaV and Syncade systems.
  • Perform Validation Maintenance of computerized systems.
  • Review/Revise CSV SOPs.
  • Perform review of Engineering documents (P&IDs, SOPs, Specifications, Submittals, etc..)
  • Assist with audits and inspections.
What we are looking for:
  • Bachelor’s degree in computer science, engineering, or related field.
  • 3+ years experience in Computer Systems Validation and in a cGMP facility.
  • 1+ years with Programmable Logic Controllers (PLC), Controls Automation, Process Control Systems, SCADA Systems, Distributed Controls Systems (DCS), Building Alarm Systems (BAS), Building Management Systems (BMS), Manufacturing Execution Systems (MES) required, DeltaV is preferred.
  • Experience leading projects and managing CAPAs and deviations.
  • Background in biotech, pharma, or medical device industry.
  • Strong attention to detail and ability to meet deadlines.
  • Ability to work independently and on-site in Portsmouth NH.
About Lonza:

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values—Collaboration, Accountability, Excellence, Passion, and Integrity—reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table.

At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.

If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

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