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Csv Validation Jobs in Oregon (NOW HIRING)

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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: $93/hr on W2 Schedule: Full-time, onsite Interview Process: Initial Teams interview followed by a ...

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Shimento, Inc.

CQV Validation Specialist

Bend, OR · On-site

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 ...

New

Staffing

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Validation Engineer 2

Bend, OR · On-site

$100 - $110/hr

CQV Validation Specialist Contractor, CSV/CQV Specialist Schedule: Full-time, onsite Interview Process : Initial Teams interview followed by a panel interview (Teams or onsite; onsite may be required)

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Sunrise Systems Inc

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Validation Engineer_26-04147

Bend, OR · On-site

$96 - $98/hr

Seeking a contractor-level CSV/CQV Specialist to support a high-priority backlog of qualification and validation activities within the CQV department. This role will provide validation support for ...

New

Natera

Comp. Sys Validation Spec

OR · On-site +1

Ensure validation state of software systems are maintained ... Act as subject matter expert for CSV compliance during internal and external audits * Perform audit ...

Syner-G

Sr. Validation Engineer

Hillsboro, OR · On-site

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

Syner-G

Sr. Validation Engineer

Hillsboro, OR · On-site

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

Syner-G

Sr. Validation Engineer

Hillsboro, OR · On-site

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

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How much do csv validation jobs pay per hour?

As of Aug 21, 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.

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

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

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

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

Csv Validation jobs near you
Infographic showing various Csv Validation job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, and 4% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $114,348 per year, or $55 per hour.

Senior CSV Engineer / MES Validation Lead

Adryan B.V

Bend, OR • On-site

$120 - $170/hr

Other

Posted 20 hours ago

Posted today

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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