EvotecEV

Validation Engineer III

Evotec is a leading biotechnology company focused on drug discovery and development, striving for innovative solutions to meet patient healthcare needs.

Evotec

Employee count: 1001-5000

Salary: 92k-127k USD

United States only

Job Title: Validation Engineer III

Location: Redmond
Department: Manufacturing
Reports To: Dir, Validation

About Us: this is who we are

At 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: Your challenge…in our journey

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 Validation Engineer III at Evotec, 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.

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:

  • A curious problem-solver with a passion for learning and growing in a dynamic environment.

  • Someone who is not satisfied with “just good enough” and is always looking to improve, adapt, and innovate.

  • A natural collaborator who loves sharing ideas and learning from others.

  • Comfortable with ambiguity and thrives in environments where curiosity and experimentation are encouraged.

  • Excellent communicator, both verbally and in writing, able to share complex ideas in a simple, relatable way.

  • A self-starter who takes initiative, owns your projects, and actively seeks out new challenges.

  • 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, process validation, utilities and facilities and analytical equipment and systems

Education and Qualification Requirements

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

  • Ability to work both independently and collaboratively across multiple disciplines in a fast-paced and dynamic environment

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, whether that means working remotely or choosing a hybrid model.

  • 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 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 $92,400 to $126,500; 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 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.

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.

About the job

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Job type

Full Time

Experience level

Senior

Salary

Salary: 92k-127k USD

Location requirements

Hiring timezones

United States +/- 0 hours

About Evotec

Learn more about Evotec and their company culture.

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Evotec is a global biotechnology company committed to advancing drug discovery and development together with our partners for medicines that matter. We strive to align patients’ healthcare needs with the industry’s demand for efficient R&D. Through scientific collaboration and partnerships, our goal is to innovate and transform lives. Our approach is designed to provide high-value pipeline co-creation partnerships and CRO/CDMO services that prioritize the quality and efficiency of R&D programs.

Our expertise covers various therapeutic areas and modalities with a strong emphasis on small molecules and biotherapeutics. We pride ourselves on collaborating closely with our partners, acting as 'drug hunters' in an effort to advance scientific research. Utilizing our industrialized, AI-powered proprietary R&D platforms, such as PanOmics and iPSC technologies, we drive better understanding of diseases and their relevance to human studies. Additionally, we deploy AI and continuous manufacturing technologies to ensure improved access to high-quality biotherapeutics, thereby enhancing the overall R&D pipeline.

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