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Csv Engineer Jobs in Oregon (NOW HIRING)

ASK Consulting

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CSV/CQV Validation Specialist (cur_1_129769@curatelyai.net)

Bend, OR · On-site

$93/hr

CSV/CQV Validation Specialist Location: Bend, OR (Onsite) Duration: 6-9 Month Contract Pay rate ... Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and ...

Staffing

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Validation Engineer 2

Bend, OR · On-site

$100 - $110/hr

Validation Engineer 2 Location: Bend OR 97703 United States Duration: 6-9 Months Job Summary ... CQV Validation Specialist Contractor, CSV/CQV Specialist Schedule: Full-time, onsite Interview ...

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Sunrise Systems Inc

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Validation Engineer_26-04147

Bend, OR · On-site

$96 - $98/hr

Validation Engineer Location: Bend, OR (Onsite) Duration: 6-9 Month Contract Position Summary ... Seeking a contractor-level CSV/CQV Specialist to support a high-priority backlog of qualification ...

Syner-G

Sr. Validation Engineer

Hillsboro, OR

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 ...

Natera

Comp. Sys Validation Spec

OR · On-site +1

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 ...

Shimento, Inc.

CQV Validation Specialist

Bend, OR · On-site

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 ...

New

Syner-G

Sr. Validation Engineer

Hillsboro, OR

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 ...

Syner-G

Sr. Validation Engineer

Hillsboro, OR · On-site

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 ...

Dynamic Solutions Technology LLC

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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$38.1K

$105.2K

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How much do csv engineer jobs pay per year?

As of Aug 22, 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:

What are popular job titles related to Csv Engineer jobs in Oregon?

For Csv Engineer jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Csv Engineer jobs in Oregon look for?

The top searched job categories for Csv Engineer jobs in Oregon are:

Csv Engineer jobs near you
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.

Senior CSV Engineer / MES Validation Lead

Adryan B.V

Bend, OR • On-site

$120 - $170/hr

Other

Posted yesterday

New

Job description

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 manufacturing environment.

The Opportunity

Adryan is looking for an experienced Senior Computer System Validation (CSV) Engineer / MES Validation Lead to support a pharmaceutical manufacturing site in Oregon. The successful candidate will take ownership of CSV activities with a strong focus on MES and related manufacturing systems, working closely with Manufacturing, Automation, Engineering, IT/OT and Quality.

Ideally someone who understands how an MES operates in a pharmaceutical manufacturing environment, can translate manufacturing processes into validated system requirements, and can drive the MES validation lifecycle from requirements through testing, release and change control.

Key Responsibilities
  • Lead and execute CSV activities for MES and associated manufacturing systems.
  • Own or lead the MES validation workstream, including planning, risk assessment, documentation, testing and release.
  • Develop and review Validation Plans, URS, functional/design specifications, risk assessments, traceability matrices, IQ/OQ/PQ protocols, test scripts and Validation Summary Reports.
  • Support implementation, configuration, upgrade, expansion and lifecycle management of MES solutions.
  • Translate manufacturing processes, electronic batch records and GMP requirements into MES system and validation requirements.
  • Apply risk-based validation in accordance with GAMP 5 and modern CSA principles where appropriae.
  • Ensure compliance with 21 CFR Part 11, EU GMP Annex 11 and Data Integrity / ALCOA+ expectations.
  • Assess changes to MES and connected systems through formal change control and validation impact assessment.
  • Support deviations, investigations, CAPAs, troubleshooting and inspection readiness related to computerized systems.
  • Validate interfaces between MES and systems such as ERP, LIMS, DCS, SCADA, PLC.
  • Coordinate effectively across Manufacturing, Automation, IT/OT, Engineering and Quality and drive validation activities to agreed milestones.
Required Experience
  • 7+ years of CSV experience in pharmaceutical, biotechnology or another regulated life-sciences environment.
  • Strong, demonstrable hands-on MES validation experience is essential.
  • Experience leading or independently owning an MES/CSV workstream.
  • Strong knowledge of GAMP 5, 21 CFR Part 11, EU GMP Annex 11, Data Integrity and risk-based validation.
  • Experience across the full computerized system lifecycle: requirements, design review, testing, qualification, release, change control and periodic review.
  • Experience working directly within a GMP manufacturing environment.
  • Ability to communicate effectively with Manufacturing, Automation, IT/OT, Engineering and QA stakeholders.
  • Strong documentation, troubleshooting and stakeholder-management skills.
  • Ability to work independently and deliver in a fast-paced project environment.
Highly Preferred
  • Experience with Werum / Körber PAS-X, Rockwell PharmaSuite, Siemens Opcenter or another enterprise MES platform.
  • MES integration with ERP, LIMS, DCS, SCADA, PLC or historian systems.
  • Electronic Batch Records (EBR/eBR), recipe management and master batch record configuration.
  • MES equipment integration, automation interfaces, data migration and system interfaces.
  • CSA / risk-based assurance approaches and validation of manufacturing automation systems.
  • Experience in Oral Solid Dosage, drug product, small-molecule manufacturing, spray drying or related pharmaceutical operations.
  • Experience in greenfield, expansion or major system implementation projects.
About Adryan

Adryan is an international engineering and quality consultancy dedicated to the pharmaceutical and biotechnology industry. We support leading life-sciences organizations across Europe and the United States with specialized expertise in Commissioning & Qualification, Computer System Validation, Quality & Compliance, Engineering and Project Management.

For this assignment we are looking for a senior professional who can make an immediate impact, strengthen our delivery in Oregon and become an important part of our growing US project organization.

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