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Full Time Computer System Validation Csv Jobs (NOW HIRING)

Alliance Biotech Solutions LLC

CSV Engineer

Raleigh, NC · On-site

The Senior Computer System Validation (CSV) Engineer is responsible for leading the validation of ... Benefits & Compensation • Industry competitive wage as a full-time employee • Flexible Paid ...

PSC Biotech

LabWare Specialist

Thousand Oaks, CA · On-site

$85K - $115K/yr

Validation & CSV Support * Support Computer System Validation (CSV) activities for LabWare implementations and enhancements. * Author and/or contribute to validation deliverables. * Ensure full ...

RESILIENCE

CSV Engineer III

West Chester, OH · On-site

Hands-on experience with automation and computer system validation (CSV). * Working knowledge of GxP regulations and validation standards for computerized systems, including 21 CFR Part 11, GAMP 5, ...

RESILIENCE

CSV Engineer III

West Chester, OH · On-site

Hands-on experience with automation and computer system validation (CSV). * Working knowledge of GxP regulations and validation standards for computerized systems, including 21 CFR Part 11, GAMP 5, ...

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How much do full time computer system validation csv jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for full time computer system validation csv in the United States is $51.80, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $64.42 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time Computer System Validation (CSV) professional, and why are they important?

To thrive as a Full Time Computer System Validation (CSV) professional, you need a solid background in computer science, life sciences, or engineering, along with expertise in regulatory compliance such as FDA or GxP requirements. Familiarity with validation protocols, risk management tools, documentation systems, and industry standards like 21 CFR Part 11 is essential. Attention to detail, problem-solving ability, and strong communication skills set high-performing CSV professionals apart. These skills ensure validated systems are reliable, compliant, and support patient safety in regulated environments.

What are some common challenges faced in a Full Time Computer System Validation (CSV) role, and how can they be addressed?

Professionals in Full Time CSV roles often encounter challenges such as keeping up with evolving regulatory requirements, managing cross-functional communication, and ensuring thorough documentation. Staying updated through continuous learning and training is vital to remain compliant with standards like FDA 21 CFR Part 11 or EU Annex 11. Collaborating closely with IT, QA, and business teams helps streamline validation processes, while developing clear protocols and checklists can improve documentation accuracy and audit readiness.

What is a Full Time Computer System Validation (CSV) specialist?

A Full Time Computer System Validation (CSV) specialist is a professional responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, comply with relevant regulatory requirements and function as intended. Their duties typically include planning, executing, and documenting validation activities for software and hardware systems. They work to ensure data integrity, patient safety, and product quality by validating that computer systems consistently produce accurate and reliable results. CSV specialists collaborate closely with IT, quality assurance, and business units to meet compliance standards such as FDA 21 CFR Part 11 or EU Annex 11. This role is crucial for companies subject to regulatory audits and inspections.
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Full Time Computer System Validation Csv jobs near you
Infographic showing various Full Time Computer System Validation Csv job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 75% Full Time, 13% Part Time, and 11% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $107,747 per year, or $51.8 per hour.
Computer Systems Validation Specialist III

Computer Systems Validation Specialist III

Lonza

Portsmouth, NH • On-site

Full-time

Retirement

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Computer Systems Validation Specialist III

Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.

The Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance. They conduct risk assessments, review change requests and test scripts, draft protocols, and oversee GMP documentation revisions. This role acts as the QA CSV representative for small and large-scale projects while providing technical guidance and mentorship to junior team members.

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.
  • 401(k) matching plan.
  • Supportive leadership and mentoring.
  • Commitment to ethical and sustainable practices.

Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

What you will do:

  • Perform all aspects of QMS process' – Change Control, Deviations,
  • CAPAs.
  • Perform Gap assessments to identify the gaps in processes and suggest remediation plans. Initiate the right Quality records (Deviations and CAPAs) to drive the remediation plan, as needed and execute all responsibilities as CSV project lead for projects.
  • Author/Review/Approve all end to end Computer system validation life-
  • cycle deliverables/activities.
  • Schedule qualification activities and personnel to meet business,
  • manufacturing, engineering and quality objectives.
  • Revise and maintain SOPs to ensure continuous improvement and
  • compliance to GROUP/CORP procedures.
  • Perform review of Engineering documents (P&IDs, SOPs, Specifications, Submittals, etc.).
  • Support Validation requests as a CSV SME, during Customer audits and inspections.

What we are looking for:

  • Bachelor's degree in computer science, engineering, or related field.
  • At least 3+ years of experience in computer systems validation.
  • 3+ years of Experience in working in a cGMP facility.
  • Experience with 21 CFR Part 11 and ISPE GAMP guidelines as they relate to Computer.
  • Systems Validation (especially for analytical computerized systems).
  • Works independently and in teams.
  • Background in biotech, pharma, or medical device industry.
  • 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 of 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.

Ready to shape the future of life sciences? Apply now.

Apply