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Validation / CSV Specialist

Las Piedras, PR · On-site

We are seeking a Validation / CSV Specialist to support validation activities within a regulated pharmaceutical manufacturing environment in Las Piedras, Puerto Rico . The ideal candidate will have ...

ASK Consulting

CSV/CQV Validation Specialist

Bend, OR · On-site

Description Job Title CSV/CQV Validation Specialist Location Bend, OR Position Description Client is seeking a contractor-level CSV/CQV Specialist to support a high-priority backlog of qualification ...

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How much do csv validation jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for csv validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What is a csv validation?

A CSV Validation job involves verifying the accuracy, consistency, and integrity of data within CSV files. This role ensures that the data conforms to predefined formats, standards, and business rules. It often includes checking for missing values, incorrect data types, and formatting errors to prevent issues in data processing. Professionals in this role may use scripts, validation tools, or manual reviews to ensure data quality and compliance.

What are the typical daily responsibilities of a csv validation professional?

CSV (Computer System Validation) Validation professionals are responsible for planning, executing, and documenting validation activities for computerized systems used in regulated industries like pharmaceuticals and biotechnology. Their daily tasks include reviewing system requirements, developing validation protocols, conducting risk assessments, performing validation testing, and documenting results in accordance with regulatory standards. They regularly collaborate with IT, quality assurance, and business stakeholders to ensure systems are compliant and audit-ready. Staying organized and detail-oriented is crucial, as each step must be carefully documented and verified for compliance. This role is dynamic and requires balancing technical tasks with frequent cross-functional communication.

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

To excel in CSV Validation, a strong background in life sciences, engineering, or a related technical discipline is essential, along with knowledge of computer system validation regulations and best practices. Familiarity with FDA 21 CFR Part 11, GAMP guidelines, and validation software tools is highly valued, and certifications such as PMP or CISA can be beneficial. Attention to detail, analytical thinking, and effective communication skills help professionals manage documentation and collaborate with cross-functional teams. These abilities ensure that systems in regulated environments are compliant, reliable, and meet industry standards for quality and data integrity.

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Csv Validation jobs near you
Infographic showing various Csv Validation job openings in the United States as of September 2026, with employment types broken down into 91% Full Time, 4% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Lead Engineer - Analytical Equipment Validation

Portsmouth, NH • On-site

Lonza
Biotechnology Research and Development • 10K+ employees
Learn more about Lonzaexternal

$104K - $137K/yr

Full-time

Retirement

Re-posted 14 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

Job description

Lead Engineer - Analytical Equipment Validation
Location: On-site, Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
The focus of the Computer Systems Validation (CSV)Lead Engineer role is to identify or create industry best practices and implement these within the framework of existing GAMP regulations. Responsibilities of the CSV Lead Engineer will include risk assessing systems, reviewing change requests and test scripts, drafting protocols and initiating and reviewing GMP documentation revisions as well as ownership of department procedures. The position provides guidance 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.
  • 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:
  • Lead collaboration between internal teams and CSV to prioritize and complete activities on time.
  • Maintain knowledge of Lonza policies, 21 CFR Part 11, Data Integrity, ICH Q7A, and GAMP principles.
  • Perform QMS processes (Change Control, Deviation, CAPA) and validation maintenance of computerized systems.
  • Participate in audits and inspections as a Subject Matter Expert.
  • Own, revise and maintain CSV SOPs.
  • Support qualification activities and documentation for CSV validation in line with regulatory guidelines.
  • Function as CSV SME in inspections and Audits,

What we are looking for:
  • Bachelor's Degree is required (preferably in Computer Science/Software Engineering).
  • 5-10 years' of Computer Systems Validation experience.
  • Experience with 21 CFR Part 11 and ISPE GAMP guidelines as they relate to Computer Systems Validation .
  • Strong written and oral communication skills.
  • Strong organizational and time management skills.

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.

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About Lonza

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Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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