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Csv Validation Jobs in Oregon (NOW HIRING)

CQV Validation Specialist / CSV/CQV Specialist Location: Bend, OR (Onsite) Duration: 6-9 Month Contract Interview Process: Initial Teams interview followed by a panel interview (Teams or onsite ...

Validation Engineer 2 CSV/CQV Specialist Location: 1201 NW Wall Street, Bend, OR 97703 Work Model: Full-Time, Onsite Contract Duration: 69 Months (Potential for Extension or Full-Time Conversion) Pay ...

Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and process validation. * Extensive experience generating protocols for automated production systems, with ...

Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and process validation. * Extensive experience generating protocols for automated production systems, with ...

Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and process validation. * Extensive experience generating protocols for automated production systems, with ...

JIRA Engineer

OR · On-site +1

$49.50 - $64.75/hr

Experience with data export, import, and validation process. * Familiar with tools or techniques for migrating data between platforms (e.g., Migration Assistant, CSV imports, API usage). * Experience ...

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Csv Validation information

See Oregon salary details

$23

$54

$82

How much do csv validation jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for csv validation in Oregon is $54.98, according to ZipRecruiter salary data. Most workers in this role earn between $41.68 and $66.83 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.

Infographic showing various Csv Validation job openings in Oregon as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $114,348 per year, or $55 per hour.

CSV Engineer - Bend, Oregon, USA

Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL)

Bend, OR • On-site

Full-time

Posted 9 days ago


Job description

AMTSOL is seeking a CSV/CQV Specialist to support high-priority qualification and validation activities within a cGMP environment. The role focuses on the qualification of analytical instruments, computerized systems and GMP equipment, and on driving inspection-ready validation documentation and backlog remediation.

Key Responsibilities

  • Support IQ/OQ/PQ for analytical instruments, computerized systems and GMP equipment.
  • Develop and execute validation documentation, including URS, risk assessments, protocols, test scripts, traceability matrices and reports.
  • Support CSV, data integrity, 21 CFR Part 11, EU Annex 11 and GMP compliance.
  • Partner with QC, QA, Engineering, Automation, Instrumentation and system owners.
  • Manage deviations, CAPAs, change controls and validation backlog activities.
  • Use Kneat for validation documentation, workflows and approvals.
  • Help drive inspection-ready documentation and backlog remediation.

Requirements

  • 3–5+ years’ experience in CQV/CSV within pharmaceutical, biotech or regulated industries.
  • Bachelor’s degree in Engineering, Life Sciences, Chemistry, Biology or a related field preferred.
  • Strong GMP / CQV / CSV background.
  • Analytical laboratory instrument qualification experience.
  • Hands-on equipment qualification experience.
  • Kneat experience strongly preferred.
  • Excellent technical writing and documentation skills.
  • Able to manage multiple priorities in a fast-paced environment.