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Senior Scientist Bioassay - Site Based, Redmond, WA

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Job Id JOB ID-13850 Standort Redmond, Washington Veröffentlichungsdatum 03/25/2026 Job Kategorie Research & Development

Job Title: Senior Scientist Bioassay

Shifts: Day, Monday to Friday, core hours 8:00am till 5:30pm

About Us: this is who we are

At JustEvotec 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 Senior Scientist 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 Senior Scientist Bioassay at JustEvotec 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.

Just is seeking a highly motivated individual who desires a significant opportunity to improve worldwide access to biotherapeutics. The QC Senior Scientist will provide the QC analysis of in-process, drug substance and drug product samples in support of our GMP manufacturing operations at the Seattle and Redmond, WA GMP facilities. These efforts support GMP manufacturing activities for biotherapeutic products. 

What You’ll Do:

  • Perform routine/non-routine QC testing using Bioassay (Cell-based Potency ELISA; PCR; HCP; ProA) methods. 

  • Ensure timely and accurate completion of GMP documentation. 

  • Collaborate with Analytical Development to generate and approve protocols, reports, and other technical documents required for the qualification and transfer of Bioassay methods. 

  • Conduct laboratory investigations, deviations, OOS, change controls and CAPAs. 

  • Support equipment qualification (IQ, OQ, PQ). 

  • Support QC management in the timely review of data. 

  • Develop, revise, and review SOPs, methods and associated documents. 

  • Support all operations of the QC labs including the ordering supplies, maintaining laboratory equipment and lab spaces, , and logbook reviews. 

  • Support client audit/inspection readiness plans and interact with regulatory agencies during inspections on Bioassay related matters. 

  • Participate in daily and weekly operation meetings. 

  • Provide on-the-floor mentorship, training and technical leadership for less experienced staff as an individual contributor. 

Who You Are:

  • BS in Chemistry, Biochemistry, or related field with a minimum of five years of Quality Control experience in GMP biopharmaceutical or biotechnology industry. 

  • Extensive laboratory experience with either Bioassay (ELISA; PCR; HCP; ProA; cell -based potency) techniques. 

  • Experience with capillary electrophoresis or chromatography data systems. 

  • Knowledge of GMP regulations and experience with regulatory compliance inspections. 

  • Ability to adapt, work in a fast-paced environment, manage multiple projects and priorities at the same time. 

  • Excellent oral/written and interpersonal communication skills; and a knowledge of Microsoft Office Suite (Excel, Word, PowerPoint). 

  • Ability to work independently and with others to accomplish goals and priorities. 

  • Must possess effective time management skills, demonstrate initiative, resourcefulness and flexibility to work independently and as part of a team. 

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. This role is site based.

  • 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 JustEvotec Biologics.

Let your curiosity guide your career—#BeCurious and explore the endless possibilities at JustEvotec Biologics!

The base pay range for this position at commencement of employment is expected to be $92,400 to $126,500; this is a salary or hourly exempt or non-exempt role. 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, 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.

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Kulturelle Passung und Soft Skills sind wichtige Erfolgsfaktoren. Mit folgenden Eigenschaften passt du gut zu uns!

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