Quality Specialist Raw Material Disposition – Quality Raw Materials (GMP)

Reports to: Sr. Director, Raw Materials

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.

About the Role

We are seeking a GMP-focused Quality Specialist Raw Material Disposition to support GMP 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 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.

Responsibilities

• Compile lot release documentation for Raw Material disposition.
• Ensure lot release deliverables are received from key stakeholders prior to Raw Material disposition.
• Support 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 Raw Material Disposition.
• Audit/inspection support for Raw Material Disposition as required.
• Partner with other QA peers to ensure consistency and efficiency within the QA department.
• Alert management of significant quality, compliance, supply, and safety risks.

Requirements

• Bachelor’s degree in biological or engineering science or equivalent work experience.
• 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.

Benefits

• Growth Opportunities: Professional courses, mentorship, and new projects to support continuous learning and development.
• Flexible Work Environment: Flexible work options to help balance professional and personal life (site-based role in Redmond).
• Inclusive Culture: A diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
• Innovative Projects: Opportunity to work on groundbreaking initiatives and cutting-edge technology.
• A Place for Big Ideas: An atmosphere where creative ideas are welcomed and explored.

Pay

The base pay range for this exempt position at commencement of employment is expected to be $87,000 to $95,000. Base salary offered may vary depending on individual’s skills, experience, and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits (Medical, Dental, and Vision), short-term and long-term disability, company-paid basic life insurance, 401k company match, flexible work options, generous paid time off and paid holidays, wellness, and transportation benefits.

Schedule

Day Shift, Monday-Friday, Core Hours 8:00am-5:30pm (Onsite in Redmond).