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Job Title: Quality Senior Specialist Raw Material Disposition - Quality Control (GMP) Shifts: Day Shift, Monday-Friday, Core Hours 8:00am-5:30pm Location: Redmond / Seattle, WA (Onsite) About Us: Who We Are At Just Evotec Biologics, curiosity fuels everything we do. We challenge assumptions, explore new ideas, and push the boundaries of what's possible in biologics development and manufacturing. As we prepare for Process License Inspections (PLI) and transition toward commercial readiness, we're building a team that thrives on scientific rigor, operational excellence, and a deep commitment to quality. If you're someone who asks bold questions, seeks meaningful answers, and isn't afraid to dive deep into complex problems-your curiosity belongs here. #BeCurious with us. The Role: Your Challenge in Our Commercialization Journey We are seeking a GMP focused Quality Senior Specialist Raw Material Disposition to support QC operations for late stage and commercial biologics manufacturing. In this role, you will be a key contributor to ensuring the quality, consistency, and regulatory compliance of raw materials across our Seattle and Redmond GMP facilities. You will play a critical role in supplier and material onboarding, audit, complaint, and disposition activities in accordance with approved procedures-all essential to our path toward commercialization. This is a role for someone who is both scientifically sharp and operationally disciplined, who can think creatively while executing flawlessly in a regulated environment. The Quality Senior Specialist Raw Material Disposition will ensure compliance of all suppliers and raw materials dispositioned 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 (GMP Heavy Responsibilities) Compile lot release documentation for Product and Raw Material disposition. Ensure lot release deliverables are received from key stakeholders prior to Product and Raw Material disposition. Facilitate weekly lot disposition meeting with QA, Manufacturing, QC, etc. Review Deviations, OOS, and Change control records to ensure no impact to Product. Lead process improvements within Lot and Raw Material Disposition. Audit/inspection support for Lot and Raw Material Disposition as required. Partners with other QA peers to ensure consistency and efficiency within the QA department. Alert senior management of significant quality, compliance, supply, and safety risks. Who You Are (Qualifications & Competencies) Requirements Bachelor's degree in biological or engineering science Minimum of 5 years relevant experience in a biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment. Ability to collaborate and communicate cross-functionally. Proven attention to detail 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 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 $92,400 to $126,500; this is a salary 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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