QC Associate Scientist - Site based, day shifts, Redmond, WA -

Job Title: QC Associate Scientist - Analytical 

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 QC Associate 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 QC Associate Scientist 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.

This role provides the QC analysis of raw materials, 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.

Shifts: Day - Wednesday to Saturday - 4 x 10 hours, 8:00 till 18:00

What You’ll Do:

• Collaborate with cross-functional teams to explore new possibilities and solutions.

• Bring fresh perspectives that challenge the status quo.

• Perform routine/non-routine QC testing using chromatographic and physiochemical 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 analytical methods.

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

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

• Create, maintain, and revise SOPs, methods and associated documents.

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

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

• Participate in daily and weekly operation meetings.

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.

• BS in Chemistry, Biochemistry, or related field. No more than 3 years experience required for this entry level role.

• Laboratory Experience with either HPLC / UPLC chromatography systems or capillary electrophoresis techniques.

• High attention to detail and organized.

• Experience with Microsoft Office apps (Word, Excel, PowerPoint).

• Experience in a cGMP environment.

• Familiarity with capillary electrophoresis or chromatography data systems.

• Experience with ELISA based methods.

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.

• Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.

• Innovat