Validation Engineer III, Cleaning & Shipping

Job Title: Validation Engineer III, Cleaning & Shipping
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.
As a Validation Engineer III, you’ll play a key role in developing and executing validation strategies supporting late-phase and commercial biologics manufacturing, with a primary focus on cleaning validation. As part of our collaborative global Validation team, you’ll partner across Operations, Logistics, Quality, Tech Transfer, Process Development, Engineering, and external vendors to develop and execute compliant, science- and risk-based validation programs.
You’ll have the opportunity to take ownership of complex validation activities, lead investigations and problem-solving efforts, and contribute to validation strategies that support our growing biologics manufacturing network. The role may also support commissioning, qualification, and validation activities for manufacturing and laboratory equipment, facilities, utilities, and systems as business needs require.
What You’ll Do:
Lead the development and execution of phase-appropriate validation deliverables supporting global CQV strategies, with a focus on cleaning and shipping validation.
Develop validation strategies and programs, including Validation Master Plans (VMPs) and supporting documentation.
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, root cause analysis, and development of appropriate corrective actions.
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: 7+ years
Strong technical expertise in cleaning validation within a GMP pharmaceutical or biologics manufacturing environment.
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
Experience leading major validation projects or programs
Working knowledge of process validation, utilities and facilities and analytical equipment/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.