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Evotec

Quality Engineer - Site based either Redmond or Seattle, WA

Job Posted 13 Days Ago Posted 13 Days Ago
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In-Office
2 Locations
77K-126K Annually
Mid level
In-Office
2 Locations
77K-126K Annually
Mid level
As a Quality Engineer at Just Evotec Biologics, you'll ensure GxP compliance in biopharmaceutical manufacturing, manage quality systems, and oversee equipment validation.
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Job Description

Job Title: Quality Engineer, QEV      

Location: Redmond, WA or Seattle, WA site based role

Department: Manufacturing

Reports To: Sr. Manager QEV

About Us: this is who we are

At Just Evotec Biologics, 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 Quality Engineer, QEV 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 Quality Engineer, QEV at Just Evotec Biologics, 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:

  • Apply knowledge of technical & validation standards/requirements and industry guidance to influence the interpretation of governing requirements as it relates to Quality Systems & Validation.

  • Understand JEB equipment management program to ensure manufacturing equipment is in a state of control, including reviewing and approving equipment calibration and preventative maintenance documents.

  • Provide Quality oversight and approval of the installation, qualification/validation, operation and maintenance of GxP equipment, and computerized systems, including infrastructure qualification.

  • Mentor functional groups in qualification/validation technical aspects, and compliance requirements.

  • Partner with both internal/external collaborators, vendors, and regulatory agencies to anticipate and resolve quality issues as well as maintain GxP compliance.

  • Perform risk assessments and data integrity evaluations in support of validation/qualification activities.

  • Travel to JEB sites as required. Onsite support at Redmond or the Seattle facility depending on site needs.

Who You Are:

  • Bachelor’s degree in biological sciences, chemistry, biochemistry, engineering, computer science or related life science field.

  • 4+ years relevant experience in a biopharmaceutical cGMP manufacturing or similar environment. 

  • Knowledge of Risk Management, Data Integrity, Industry guidelines, US & EU regulatory requirements.

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 Just Evotec Biologics

Let your curiosity guide your career—#BeCUREious and explore the endless possibilities at Just Evotec Biologics!

The base pay range for this position at commencement of employment is expected to be $77,000 to $126,000; 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.

Top Skills

Cgmp
Computerized Systems
Data Integrity
Quality Systems
Risk Management
Us & Eu Regulatory Requirements
Validation Standards

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