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Csv Engineer Jobs in Oregon (NOW HIRING)

Validation Engineer 2

Bend, OR · On-site

$70.92 - $99.29/hr

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 ...

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and ...

Computer System Validation Specialist will work the Natera Software Engineering team to ensure ... Act as subject matter expert for CSV compliance during internal and external audits * Perform audit ...

Bachelor''s Degree in Engineering, Life Sciences, Chemistry, Biology, or a related scientific discipline preferred. Experience * Minimum 3-5 years of CQV and/or CSV experience within pharmaceutical ...

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and ...

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and ...

JIRA Engineer

OR · On-site +1

$49.50 - $64.75/hr

Dynamic Solutions Technology, LLC (DST) is seeking a full time JIRA Engineer to lead a migration ... CSV imports, API usage). * Experience migrating and supporting Jira plugins (e.g., Jira Workflow ...

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Showing results 1-20

Csv Engineer information

See Oregon salary details

$38.1K

$105.2K

$145.5K

How much do csv engineer jobs pay per year?

As of Aug 30, 2026, the average yearly pay for csv engineer in Oregon is $105,214.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,500.00 and $123,300.00 per year, depending on experience, location, and employer.

What is a CSV engineer?

A CSV (Computer System Validation) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, comply with regulatory requirements. They develop validation protocols, perform testing, document results, and ensure adherence to industry standards like FDA 21 CFR Part 11 and GAMP 5. Their goal is to confirm that software and hardware systems function correctly, maintain data integrity, and meet compliance requirements.

What are the key skills and qualifications needed to thrive as a CSV engineer?

To thrive as a CSV Engineer (Computer System Validation Engineer), you need a solid understanding of validation principles, regulatory compliance (such as FDA 21 CFR Part 11), and a relevant degree in life sciences, engineering, or information technology. Familiarity with validation lifecycle documentation, risk assessment tools, and industry-standard systems like SAP, LIMS, and TrackWise is highly valued, as are certifications such as GAMP or Six Sigma. Strong attention to detail, analytical thinking, and excellent communication skills help CSV Engineers collaborate efficiently with cross-functional teams and ensure thorough documentation. These skills are crucial to guarantee that computerized systems in regulated industries meet compliance requirements, supporting product quality and patient safety.

What are the common challenges faced by a CSV engineer in the pharmaceutical or medical device industry?

CSV Engineers in the pharmaceutical or medical device industry often face the challenge of keeping up with evolving regulatory requirements and ensuring all computerized systems remain compliant throughout their lifecycle. Managing comprehensive documentation, coordinating with multiple departments, and troubleshooting complex system changes can add to the workload. Successful CSV Engineers are proactive about staying informed of regulatory updates, are highly organized, and collaborate closely with Quality Assurance, IT, and operations teams. This dynamic environment offers the opportunity to learn continuously, develop expertise in validation best practices, and advance into leadership or specialized quality roles.

How much do CSV engineers make?

CSV engineers typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and industry. They often work with data processing tools and scripting languages like Python or SQL to manage and analyze CSV data efficiently.

How to become a CSV engineer?

To become a CSV engineer, you should develop strong skills in data management, scripting languages like Python or SQL, and familiarity with CSV file formats. Earning relevant certifications or degrees in data science, computer science, or related fields can also enhance your qualifications, along with experience working with data processing tools and environments.

What are the most commonly searched types of Csv Engineer jobs in Oregon?

The most popular types of Csv Engineer jobs in Oregon are:

Infographic showing various Csv Engineer job openings in Oregon as of August 2026, with employment types broken down into 100% Full Time. Highlights an 71% In-person, and 29% Remote job distribution, with an average salary of $105,214 per year, or $50.6 per hour.

CSV Engineer - Bend, Oregon, USA

Bend, OR • On-site

Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL)

Full-time

Posted 7 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.