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Csv Validation Jobs (NOW HIRING)

Valspec

Validation Engineer (CSV)

Seattle, WA

Lead Validation Engineer (CSV / DeltaV) Valspec | Seattle, WA Full-Time | Hybrid Client Site Support About Valspec Valspec, part of the Proconex family of companies, is a leading provider of Computer ...

Valspec

Validation Engineer (CSV)

Redmond, WA · On-site

Lead Validation Engineer (CSV / DeltaV) Valspec | Seattle, WA Full-Time | Hybrid Client Site Support About Valspec Valspec, part of the Proconex family of companies, is a leading provider of Computer ...

Validation & Engineering Group, Inc

PR

Computer System Validation (CSV) Specialist Project summary: * Validate and support the Electronic Batch Record / EVRS implementation so it meets 21 CFR Part 11, EU GMP Annex 11, GxP, and company ...

Lonza

WI · On-site

$80 - $120/hr

As the Computer System Validation (CSV) Expert you will report directly to the local CSV manager and be the domain expert responsible for implementing Computer System Validations at our site in ...

Adryan B.V

$120 - $170/hr

We are looking for a senior CSV professional with strong, hands-on Manufacturing Execution System (MES) validation experience who can independently lead an MES validation workstream in a GMP ...

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Csv Validation information

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How much do csv validation jobs pay per hour?

As of Aug 22, 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 August 2026, with employment types broken down into 1% As Needed, 90% Full Time, 4% Part Time, and 5% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Bloomington CQV/CSV Validation Engineers

Verista, Inc.

Bloomington, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago

Job description

Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Join Our Team: Validation Engineers Wanted in Bloomington, IN!
Are you a skilled Validation Engineer with a passion for ensuring quality in the pharmaceutical industry? Verista is actively seeking talented professionals to join our team in the vibrant Bloomington, IN area!
Who We're Looking For:
  • Experience: 3+ years in validation engineering within pharmaceuticals or biotech.
  • Skills: Expertise in equipment qualification, Delta V, Upstream/Downstream process validation, GMP compliance, CIP/SIP, HVAC, or Utilities.
  • Location: Based in or willing to relocate to Bloomington, IN.
  • Passion: Dedicated to delivering high-quality solutions that ensure patient safety and regulatory compliance.
What We Offer:
  • Exciting projects with leading pharmaceutical companies.
  • Competitive compensation and benefits based on proven experience.
  • Opportunities for professional growth and development.
  • A collaborative, innovative work environment in the heart of the Research Triangle.

Ready to make an impact? Apply for more details. Let's shape the future of pharmaceuticals together!
#PharmaJobs #ValidationEngineer #Bloomington #Hiring #ExpertsDeliveringSolutions
Benefits
Why Choose Verista?
  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com

Apply