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Validation Engineer Iii Jobs (NOW HIRING)

Validation Engineer III Location: Redmond, WA Reports to: Director, Validation About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward ...

Validation Engineer III Location: Redmond, WA Reports to: Director, Validation About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward ...

Validation Engineer III Location: Redmond, WA Reports to: Director, Validation About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward ...

Validation Engineer III Location: Redmond, WA Reports to: Director, Validation About Us: At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward ...

Validation Engineer III Location: San Diego, CA Duration: 7 Month Assignment Validation Engineer- Contract Abbott Rapid Diagnostics (formerly Alere) is part of Abbott's Diagnostics family of ...

... 3+ years of significant engineering and/or operational experience. * Experience in the development of commissioning, qualification, validation and risk management deliverables including ...

... 3+ years of significant engineering and/or operational experience. * Experience in the development of commissioning, qualification, validation and risk management deliverables including ...

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Validation Engineer Iii information

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How much do validation engineer iii jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for validation engineer iii in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What is the difference between Validation Engineer Iii vs Validation Engineer Ii?

AspectValidation Engineer IiiValidation Engineer Ii
Required CertificationsGMP, GxP, or industry-specific validation certificationsGMP, GxP, or industry-specific validation certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingPharmaceutical, biotech, or medical device manufacturing
Experience LevelAdvanced, with 3+ years of validation experienceIntermediate, with 1-3 years of validation experience
Job ResponsibilitiesLeading validation projects, complex troubleshooting, mentoringSupporting validation activities, executing protocols

The Validation Engineer Iii typically has more experience and handles complex validation projects, often leading initiatives and mentoring junior staff. In contrast, Validation Engineer Ii focuses on supporting validation tasks and executing protocols under supervision. Both roles are common in regulated industries like pharmaceuticals and biotech, with the Iii level requiring more expertise and responsibility.

What are the key skills and qualifications needed to thrive as a Validation Engineer III, and why are they important?

To excel as a Validation Engineer III, you need a strong background in engineering or life sciences, extensive knowledge of validation protocols, and experience in regulated industries such as pharmaceuticals or medical devices. Familiarity with technical tools like validation lifecycle management software, statistical analysis packages, and regulatory standards (e.g., FDA, GMP) is typically required, along with relevant certifications such as Six Sigma or CQE. Critical thinking, attention to detail, and effective communication are crucial soft skills for documenting processes and collaborating with cross-functional teams. These competencies ensure compliance, product quality, and the successful execution of complex validation projects.

What are Validation Engineer III roles and responsibilities?

A Validation Engineer III is responsible for ensuring that products, processes, and systems meet regulatory and company standards for quality and safety. This role typically involves planning and executing validation tests, writing protocols and reports, analyzing data, and troubleshooting validation issues. Validation Engineer IIIs often lead validation projects, mentor junior staff, and work closely with cross-functional teams in industries like pharmaceuticals, biotechnology, or manufacturing. They ensure compliance with regulatory requirements such as FDA, GMP, or ISO standards. Strong analytical, documentation, and project management skills are important for success in this position.

What are some common challenges faced by a Validation Engineer III, and how can they be addressed?

As a Validation Engineer III, one common challenge is coordinating among cross-functional teams such as manufacturing, quality, and regulatory departments to ensure validation activities meet strict compliance standards and timelines. Managing multiple projects simultaneously while adhering to evolving regulatory requirements can also be demanding. Strong project management, effective communication, and staying updated on industry guidelines help address these challenges and ensure successful validation outcomes.
More about Validation Engineer Iii jobs
What states have the most Validation Engineer Iii jobs? States with the most job openings for Validation Engineer Iii jobs include:

Validation Engineer III

Evotec

Redmond, WA โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago


Job description

Job Title: Validation Engineer III

Location: Redmond, WA

Reports to: Director, Validation

About Us:

At Just-Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged, it's celebrated.

Are you someone who asks questions, seeks answers, and isn't afraid to go deeper?#BeCureious with us and see where your curiosity can take you!

The Role:

We're looking for a passionate and curious Validation Engineer III to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.

Just-Evotec is seeking a highly motivated Validation Engineer III that desires a significant opportunity to improve worldwide access to biotherapeutics. A few focus areas of this job include to strategize, implement and support cleaning, shipping and process validation activities required for late phase and commercial biologics manufacturing as part of a fast-paced and collaborative global validation team. Manufacturing and laboratory equipment, systems, facilities, and utilities commissioning, qualification and validation activities maybe supported as part of this role as required.

What You'll Do:

  • Lead the generation of key deliverables in a phase appropriate compliance manner as part of global CQV strategy for F&U, Equipment, QC/Analytical, Cleaning and Shipping
  • Document a strategy for validations programs including the generation of validation master plans
  • Liaise with the equipment, operations, logistics, qc, tech transfer, process development teams and third-party contractors, as applicable, to define and identify and perform cycle development, qualification and validation activities
  • Author validation documentation including, but not limited to, risk and gap assessments, cycle development protocols / reports / procedures,qualification/validation protocols and reports, and validation discrepancies.
  • Lead validation discrepancy resolution including troubleshooting and root cause analysis
  • Support the development of the qualification and validation programs at Just including the transition from paper based to digital validation software to configure globally scalable end to end paperless solutions to manage the validation lifecycle
  • Develop and strategize compliant and novel ways to comply with regulatory requirements
  • Support inspection readiness activities, Health Authority and Client audits, and support corrective actions based on audit findings
  • Lead CQV activities across global expansion sites

Who You Are:

  • Bachelor's degree in engineering science or related program with the following years in relevant experience:Validation Engineer III - 7+ years
  • Understanding of industry standards and best practices for a science and risk-based approach to qualification of systems and processes
  • Working knowledge of US FDA CFRs and European EMA, including ICH regulations
  • Experience with quality risk management
  • Experience authoring, reviewing, and approving validation documentation
  • Knowledge of process equipment, utilities, operations, and engineering principles
  • Must possess a strong focus on quality and attention to detail
  • Must possess problem-solving and critical thinking skills
  • Motivated, self-starter with strong mechanical aptitude
  • Ability to work both independently and collaboratively across multiple disciplines in a fast-paced and dynamic environment
  • Excellent interpersonal, team, and communication skills are a must
  • High level oral and written communication skills are a must
  • Possess effective task/time management organizational skills

Additional Qualifications:

  • Applies knowledge and expertise to solve complex technical problems
  • Significant contributor to multi-disciplinary teams at the functional level
  • Led a team or large validation projects
  • Working knowledge of shipping and cleaning
  • Working knowledge of process validation
  • Working knowledge of utilities and facilities
  • Working knowledge of computerized system
  • Working knowledge of analytical equipment and systems

Why Join Us:

  • Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow.
  • Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged.
  • Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
  • A Place for Big Ideas: We don't just talk about thinking outside the box-we throw the box away. If you've got ideas, we want to hear them.

Are You Still Curious?

If you've read this far, then chances are you've got a curious mind-just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you and how it will shape the future of Just-Evotec.

Let your curiosity guide your career #BeCurious and explore the endless possibilities at Evotec!

The base pay range for this position at commencement of employment is expected to be $115,000 to $126,500; Base salary offered may vary depending on individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.

Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.