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Director Validation Jobs in Oregon (NOW HIRING)

Medline

Sr Engineer Software Validation

Redmond, OR · On-site

$101K - $152K/yr

Direct experience operating in a medical device QMS environment, including FDA 21 CFR Part 820, ISO 13485, ISO 14971, General Principals of Software Validation, Electronic Records/Signatures.

Medline

Sr Engineer Software Validation

Redmond, OR · On-site

$101K - $152K/yr

Direct experience operating in a medical device QMS environment, including FDA 21 CFR Part 820, ISO 13485, ISO 14971, General Principals of Software Validation, Electronic Records/Signatures.

Medline

Sr Engineer Software Validation

Redmond, OR · On-site

$101K - $152K/yr

Direct experience operating in a medical device QMS environment, including FDA 21 CFR Part 820, ISO 13485, ISO 14971, General Principals of Software Validation, Electronic Records/Signatures.

Natera

OR

$79K - $108K/yr

We are seeking a Director, Clinical Science to architect trial strategies and protocol execution ... This clinical leadership role shapes the data validation pipeline for our cell-free DNA (cfDNA ...

University Of Oregon

Medical Director

Eugene, OR

$245K - $260K/yr

Medical Director Apply now Job no: 536756 Work type: Officer of Administration Location: Eugene, OR ... date of employment Valid Drug Enforcement Administration certification for prescription of ...

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Director Validation information

What are the typical daily responsibilities of a Director Validation in a regulated industry?

A Director Validation typically oversees the planning, execution, and review of validation projects to ensure compliance with regulatory requirements. Daily responsibilities include leading teams, reviewing validation protocols and reports, coordinating with quality, engineering, and regulatory departments, and addressing any deviations or issues that arise during validation activities. The role may also involve direct communication with regulatory agencies during audits and inspections. This ensures products or processes meet the highest standards of quality and regulatory compliance, ultimately supporting the company’s overall operational success.

What does a Director of Validation do?

A Director of Validation oversees the validation processes in industries like pharmaceuticals, biotechnology, or medical devices to ensure compliance with regulatory standards. They develop and implement validation strategies for equipment, processes, and systems, ensuring they meet quality and safety requirements. This role involves managing validation teams, coordinating with regulatory bodies, and maintaining documentation to support audits and inspections. The Director also ensures adherence to industry guidelines such as FDA, EMA, or ISO standards.

What are the key skills and qualifications needed to thrive in the Director Validation position, and why are they important?

To thrive as a Director Validation, you need extensive experience in validation processes, regulatory compliance, quality assurance, and a relevant scientific or engineering degree. Familiarity with industry standards, validation lifecycle management software, and certifications such as Six Sigma or PMP are highly valued. Strong leadership, strategic thinking, and excellent communication skills help to drive complex projects and foster cross-functional collaboration. These skills are vital to ensuring validated processes meet regulatory standards and support organizational goals efficiently.

What are the most commonly searched types of Validation jobs in Oregon? The most popular types of Validation jobs in Oregon are:
What are popular job titles related to Director Validation jobs in Oregon? For Director Validation jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Director Validation jobs in Oregon look for? The top searched job categories for Director Validation jobs in Oregon are:
Director Validation jobs near you
Infographic showing various Director Validation job openings in Oregon as of July 2026, with employment types broken down into 1% As Needed, 86% Full Time, 10% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.
Senior Validation Engineer

Senior Validation Engineer

Intellectt INC

Portland, OR • On-site

Contractor

Posted 29 days ago

Job description

Hello, 
I Hope you are doing great. 

This is Mahaboob from Intellectt INC; we’ve got an important Senior Validation Engineer - Oregon with one of our prestigious clients. Interested candidates can please send your updated resume at mahaboob.m@intellectt.com

Title: Senior Validation Engineer
Location: Oregon

Summary: Seeking a Senior Validation Engineer with strong GMP experience to support QC equipment validation and Computer System Validation (CSV) activities.
Key Responsibilities:

  • Author & execute URS, IQ/OQ/PQ, risk & data integrity assessments
  • Support CSV (ValGenesis preferred)
  • Manage full lifecycle of QC equipment (qualification to requalification)
  • Support analytical method transfers & vendor coordination
  • Ensure compliance with GMP & ALCOA+

Requirements:

  • 5+ years validation experience in GMP environment
  • Hands-on with HPLC, GC, bioassay systems
  • Strong CQV, QC Equipment & CSV experience

Thanks & Regards,
Mahaboob M
Technical Recruiter
Intellectt Inc 
mahaboob.m@intellectt.com
Direct: 732-276-1830
Desk number: 732 412 6999- Ext: 355