Quality Specialist Raw Material Disposition – Quality Raw Materials (GMP)
Evotec
August 15, 2026
On-site
Redmond, WA
Operations
The Role
We are seeking a GMP focused Quality Specialist Raw Material Disposition to support GMP operations for late stage and commercial biologics manufacturing, ensuring the quality, consistency, and regulatory compliance of raw materials across Seattle and Redmond GMP facilities.
What You’ll Do (GMP Heavy 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 meetings 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.
- Provide 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.
Who You Are (Qualifications)
- Bachelor’s degree in biological or engineering science or equivalent work experience.
- Minimum 5 years relevant experience in biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment.
- Ability to collaborate and communicate cross-functionally.
- Proven attention to detail.
Application Instructions
- Apply today.
We are seeking a GMP focused Quality Specialist Raw Material Disposition to support GMP operations for late stage and commercial biologics manufacturing, ensuring the quality, consistency, and regulatory compliance of raw materials across Seattle and Redmond GMP facilities.
What You’ll Do (GMP Heavy 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 meetings 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.
- Provide 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.
Who You Are (Qualifications)
- Bachelor’s degree in biological or engineering science or equivalent work experience.
- Minimum 5 years relevant experience in biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment.
- Ability to collaborate and communicate cross-functionally.
- Proven attention to detail.
Application Instructions
- Apply today.