QC Associate Scientist - Raw Materials - Site Based, Redmond, WA at Evotec

Redmond, Washington, United States -

Full Time

Start Date

Immediate

Expiry Date

14 Mar, 26

Salary

83000.0

Posted On

14 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

QC Testing, Cell-Based Assays, ELISA, qPCR, GMP Documentation, Collaboration, Laboratory Investigations, SOPs, Microsoft Office, Attention to Detail, Organizational Skills

Industry

Biotechnology Research

Description

Job Title: QC Associate Scientist - Raw Materials Shifts: Days, Monday to Friday, 8:00am/8:30am till 5:00pm/5:30pm, Some flexibility required for business needs. 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 - Raw Materials 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 - Raw Materials 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. Position The role provides the inspection, sampling, and QC analysis of raw materials and supplies in support of our GMP manufacturing operations. What You’ll Do: Perform routine/non-routine QC testing using by techniques such as cell-based assays, ELISA, and qPCR. Ensure timely and accurate completion of GMP documentation. Collaborate with Supply Chain, Supplier Quality, Materials Management, and external contract laboratories to qualify and release raw materials. 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: Bachelor’s degree in chemistry or related science with 0-3 years experience in related field (GMP experience preferred). Knowledge of current instrumentation and procedures used in an analytical laboratory. High attention to detail and organized. Experience with Microsoft Office apps (Word, Excel, PowerPoint). 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 Redmond. 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—#BeCurious and explore the endless possibilities at Just Evotec Biologics! The base pay range for this position at commencement of employment is expected to be $78,000 to $83,000; 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. Just – Evotec Biologics, wholly owned by Evotec SE, is a first-to-industry biologics platform that leverages AI/ML technologies and world-leading molecular design, cell line development, process intensification and continuous manufacturing strategies to advance biotherapeutics from discovery through clinical stages to commercial launch. The Just – Evotec Biologics team combines deep industry experience in the fields of data, protein, process, and manufacturing sciences including automation with highly integrated and flexible capabilities to break through the scientific and economic barriers associated with the development of protein therapeutics. Our focus is to accelerate and expand access to biotherapeutics through scientific and technological innovation for our proprietary projects and on behalf of our partners. Learn more at www.just-evotecbiologics.com.

Responsibilities

The role involves inspection, sampling, and QC analysis of raw materials to support GMP manufacturing operations. Responsibilities include performing routine and non-routine QC testing, ensuring GMP documentation accuracy, and collaborating with various teams.