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Validation Engineer Ii Jobs (NOW HIRING)

Position Summary Validation Engineer II will be responsible for leading the commissioning, qualification, and validation (CQV) for a newly announced facility expansion for biologics that includes a ...

Validation Engineer

Raleigh, NC ยท On-site

$80K - $83K/yr

About the job Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Raleigh, NC The Level II Validation Engineer/Specialist reports directly to the ...

Perform validation activities for equipment, utilities, facilities, processes, and/or automation ... Collaborate with cross-functional teams (Manufacturing, Quality, Engineering, etc.) to support ...

Validation Engineer

Kenosha, WI ยท On-site

$50 - $55/hr

Work overnight 12-hour shifts on a 2-2-3 schedule. Requirements * Minimum 3 years of Validation Engineer experience required. * Minimum 5 years of experience preferred for Senior Validation Engineer ...

Serve as the Validation Engineering representative and technical subject matter expert (SME) on cross-functional and multi-site teams related to equipment, computerized systems, utilities, facility ...

Bachelor's degree in Engineering, Industrial Technology, Computer Science, or a related field * 0-2 ... Basic familiarity with validation terminology and concepts such as IQ, OQ, and PQ * Strong ...

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Validation Engineer Ii information

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How much do validation engineer ii jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for validation engineer ii 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 are the key skills and qualifications needed to thrive in the Validation Engineer Ii position, and why are they important?

To thrive as a Validation Engineer II, you need a strong background in engineering principles, quality assurance methodologies, and experience with validation protocols, typically supported by a bachelor's degree in engineering or a related field. Proficiency with industry-specific tools such as statistical analysis software, ERP systems, and knowledge of regulatory standards like GMP or ISO is highly valued, and certifications like ASQ are advantageous. Excellent problem-solving, attention to detail, and effective communication are key soft skills for this role. These competencies are essential to ensure products and processes meet rigorous compliance and quality standards, minimizing risks and ensuring project success.

What are the typical responsibilities of a Validation Engineer II?

A Validation Engineer II is responsible for planning, executing, and documenting validation activities for equipment, systems, and processes to ensure compliance with industry and regulatory standards. This includes developing and reviewing protocols, analyzing test data, troubleshooting issues, and supporting audits or inspections. You can expect to work closely with cross-functional teams such as quality assurance, manufacturing, and R&D to coordinate validation efforts and implement continuous improvements. The role offers opportunities to expand both technical expertise and project management skills, making it a strong stepping stone for career advancement in engineering and quality fields.

What is a Validation Engineer II job?

A Validation Engineer II is responsible for ensuring that processes, systems, and products meet regulatory and quality standards. They develop and execute validation protocols, perform testing, analyze data, and document results to maintain compliance with industry regulations. This role typically requires experience in validation methods, technical problem-solving, and collaboration with cross-functional teams. Validation Engineers II work in industries such as pharmaceuticals, medical devices, and manufacturing to ensure product reliability and safety.

More about Validation Engineer Ii jobs
What cities are hiring for Validation Engineer Ii jobs? Cities with the most Validation Engineer Ii job openings:
What are the most commonly searched types of Validation Engineer Ii jobs? The most popular types of Validation Engineer Ii jobs are:
Infographic showing various Validation Engineer Ii job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, 4% Part Time, and 4% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Validation Engineer II - Site Based, Redmond, WA

Validation Engineer II - Site Based, Redmond, WA

Just - Evotec Biologics, Inc.

Seattle, WA โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago


Job description

Job Title: Validation Engineer II

Location: Redmond, Seattle, WA

Shifts: Monday to Friday, 8:00am till 5:00pm

Some flexibility as may be required, as business needs to come in over the weekend.

About Us: this is who we are

At Just Evotec Biologic, 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: / your challenge, ...in our journey

We're looking for a passionate and curious Validation Engineer II 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.

As a Validation Engineer II at Just Evotec Biologic, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's a role where your curiosity will fuel both your personal growth and the success of the team.

The primary focus of this job is to support manufacturing and laboratory equipment, systems, facilities, and utilities commissioning, qualification and validation activities required in early phase manufacturing to late-stage programs into PPQ/ commercial biologics manufacturing. These responsibilities span all phases of the lifecycle from system implementation and qualification to cleaning and shipping validation. This role will also work cross functionally and collaborate with other teams on validation projects.

What You'll Do:

Execute FUSE commissioning and validation activities for early stage clinical manufacturing, late-stage molecule/ commercial manufacturing and/or PPQ campaign support.

Generate and review technical documentation including validation lifecycle documents, validation protocols and associated reports related to the equipment validation lifecycle.

In collaboration with cross functional teams, develop Validation Master Plans, provide process knowledge to support the validation execution and risk assessments.

Lead the development and implementation of templates and validation workflows.

Support the generation of governance policies and related SOPs for commissioning of FUSE.

Support validation deviation resolution including troubleshooting and root cause analysis

Support the periodic review of qualified/validated FUSE across JUST WA sites.

Support inspection readiness activities, Health Authority and Client audits, and support corrective actions based on audit findings

Who You Are:

Bachelor's degree in engineering science or related program with minimum 2 years relevant experience.

Proven experience in executing commissioning and validation activities of FUSE.

Understanding of GMP concepts and Quality systems necessary to execute validation activities.

Understanding of industry standards and best practices for a science and risk-based approach to qualification of systems, equipment, utilities, and/or facilities

Knowledge of process equipment, utilities, operations, and engineering principles

Experience in quality risk management

Must possess problem-solving and critical thinking skills

Good interpersonal, team, and collaborative 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

Proven knowledge of cGMP requirements and experience writing manufacturing technical documents

Experience leading technical projects and managing timelines with external collaborators and vendors

Candidate must possess a strong focus on quality and attention to detail as well as effective task/ time management organizational skills

Additional Preferred Qualifications:

Understanding of biologics manufacturing process and process automation (e.g. DeltaV)

Experience with single-use technologies and systems

Previous work experience with Complex Equipment, Distributed Control System (DCS), Building Automation Systems (BAS), PLC, SCADA, PI, and MES will be a plus

Working knowledge of utilities and facilities, computerized systems, analytical equipment, process validation and clean validation methodologies.

Significant contributor to multi-disciplinary teams at the functional level

Authority inspection or audit support involvement.

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.

  • Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based role.

  • 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 Biologic.

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

The base pay range for this position at commencement of employment is expected to be $79,800 to $109,250; Base salary offered may vary depending on the 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.