Quality Senior Specialist, Raw Material Disposition - Site Based, Redmond and Seattle, WA

Job Title Quality Senior Specialist Raw Material Disposition – Quality Control (GMP) Location Redmond / Seattle, WA (Onsite) Shift Day Shift, Monday–Friday, Core Hours 8:00am–5:30pm About Us 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. Role Overview 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. 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. Partner with other QA peers to ensure consistency and efficiency within the QA department. Alert senior management of significant quality, compliance, supply, and safety risks. Qualifications and Competencies 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. Salary 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. Equal Opportunity Employer 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. #J-18808-Ljbffr Evotec WD