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

Evotec•Redmond, WA

9d•$92,400 - $126,500•Onsite

About The Position

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. 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.

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

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.