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Validation Manager Jobs in Seattle, WA (NOW HIRING)

Actalent

Sr. Hardware Validation Engineer

Redmond, WA

$65 - $80/hr

Salaried Managed Service Top Skills Power supply testing Analog circuit testing PCB Troubleshooting and debug experience Experience writing test plans The Hardware Validation Engineer plays a key ...

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Protingent

Hardware R&D Validation Engineer

Bellevue, WA · On-site

$45 - $70/hr

Firmware & Environment Management: Flash and debug firmware (MCU/FPGA), manage Linux-based test ... Validation Tooling: Experience designing custom test fixtures or "bed-of-nails" setups to automate ...

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Validation Manager information

See Seattle, WA salary details

$54.1K

$120K

$182.7K

How much do validation manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for validation manager in Seattle, WA is $119,965.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,800.00 and $150,200.00 per year, depending on experience, location, and employer.

What is a validation manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

What are the key skills and qualifications needed to thrive as a validation manager, and why are they important?

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

How does a validation manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What is the difference between Validation Manager vs Quality Assurance Specialist?

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

More about Validation Manager jobs

What are the most commonly searched types of Validation jobs in Seattle, WA?

The most popular types of Validation jobs in Seattle, WA are:

What are popular job titles related to Validation Manager jobs in Seattle, WA?

For Validation Manager jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Validation Manager jobs in Seattle, WA look for?

The top searched job categories for Validation Manager jobs in Seattle, WA are:

What cities near Seattle, WA are hiring for Validation Manager jobs?

Cities near Seattle, WA with the most Validation Manager job openings:

Validation Manager jobs near you
Infographic showing various Validation Manager job openings in Seattle, WA as of August 2026, with employment types broken down into 83% Full Time, 15% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $120,033 per year, or $57.7 per hour.

Specialist, Quality Assurance Validation

Lyell Immunopharma

Bothell, WA • On-site

$96K - $120K/yr

Full-time

Re-posted 11 days ago

Job description

The Quality Assurance Specialist provides QA oversight for Facility, Equipment, Utility (FEU), and Computer System (CS) programs in a cell therapy manufacturing environment, with accountability for review, approval, escalation, and lifecycle compliance activities that support GMP readiness and sustained operational control.

This role serves as the Quality representative on cross-functional project teams and ensures Facility, Equipment, Utility, and Computer System activities are planned, executed, documented, and maintained in compliance with GMP requirements while supporting clinical and commercial operating timelines.

KEY ROLES AND RESPONSIBILITIES:Commissioning, Qualification, and Validation
  • Provide QA compliance oversight for Facility, Equipment, Utility, and Computer System qualification and validation projects.
  • Review and approve validation plans, User Requirement Specifications (URS), protocols (IQ/OQ/PQ), and summary reports for equipment and systems.
  • Maintain oversight of the qualified and validated state of Facility, Equipment, Utility , and computer systems through periodic review, requalification, deviation review, and change management.
  • Create and manage qualification and validation project schedules.
Facility, Equipment, and Utility Oversight
  • Support onboarding of new Facility, Equipment, and Utility assets by approving initial release requirements and defining quality expectations for lifecycle management.
  • Provide QA oversight for the calibration and maintenance programs to ensure ongoing GMP compliance and operational readiness.
  • Review and approve work plans including procedure, test points, tolerances, and acceptance criteria.
  • Review and approve asset removal, return-to-service activities, and associated quality documentation.
  • Review and approve on-demand work orders for unplanned events and repairs.
Quality Systems:
  • Review and approve Standard Operating Procedures related to Facility, Equipment, Utility, and Computer System operation and maintenance.
  • Review and approve change controls, deviations, and Corrective and Preventive Actions (CAPAs) related to Facility, Equipment, Utility , and Computer Systems.
KNOWLEDGE SKILLS AND ABILITIES:
  • Understanding of requirements and expectations for compliant Facility, Equipment, and Utility programs including commissioning/qualification, calibration, and maintenance.
  • Ability to work effectively both independently and cross-functionally.
  • Fast learner, adaptable, and has the desire and ability to work in a fast-paced, start-up environment.
  • Excellent communication, emotional intelligence and interpersonal skills.
  • Familiar with quality management systems (e.g. deviations, CAPAs, change management).
  • Curious and proactive mindset with a continuous improvement orientation.
REQUIRED EDUCATION AND EXPERIENCE:
  • Bachelor's degree in life sciences or a related technical discipline with a minimum of 5 years of experience in a GMP biopharmaceutical manufacturing environment or equivalent combination of relevant education, training, and experience,
PREFERRED EXPERIENCE:
  • Prior experience in a Quality Assurance oversight role for Facility, Equipment, and Utility qualification and management.
  • Experience with computer system validation.
  • Previous experience using Blue Mountain computerized maintenance management software.
  • Experience with cell therapy and/or lentiviral manufacturing operations.
  • Experience in commercial manufacturing and post-approval lifecycle management.
PHYSICAL REQUIREMENTS:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. While performing their duties, the employee must be able to do the following:

  • Stand and step over a gowning bench (12-24") and aseptically don head-to-toe non-sterile and sterile gowns.
SHIFT WORK, WEEKEND WORK AND HOLIDAY COVERAGE:

While this position is primarily Monday - Friday, occasional off-shift work, weekend work, and holiday work may be required due to the nature of our autologous cell therapies and the need to deliver life-saving treatments to our patients as timely as possible.

 
The salary range for this position is $96,000 to $120,000, annually, with the opportunity to earn an annual bonus. The salary range is an estimate, and the actual salary may vary based on Lyell's compensation practices and an applicant's qualifications and experience. Employees are also eligible to participate in Lyell's Equity Incentive Plan. 
At Lyell, we believe that highest performing teams include people from a wide variety of backgrounds and experiences who respectfully challenge each other. We are committed to building an open, diverse and inclusive culture for all employees.
Lyell is proud to be an equal opportunity employer and does not discriminate on the basis of race, color, citizenship status, national origin, ancestry, sex, sexual orientation, age, religion, creed, physical or mental disability, medical condition, marital status, veteran status or any other characteristics protected under applicable federal, state and local laws.
 
We've learned from experience that some of the best people don't always match our requirements perfectly - if you're interested and think you could fit, please don't hesitate to apply.

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