Quality Senior Specialist, Raw Material Disposition - Site Based, Redmond and Seattle, WA
Evotec
July 01, 2026
On-site
Redmond, WA
Operations
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 meetings 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.
- Provide 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/Requirements:
- Bachelor’s degree in biological or engineering science.
- Minimum 5 years relevant experience in biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment.
- Ability to collaborate and communicate cross-functionally.
- Proven attention to detail.
Benefits (as stated): discretionary annual bonus; Medical, Dental, Vision; short-term and long-term disability; company paid basic life insurance; 401k company match; paid time off and paid holiday; wellness and transportation benefits.
Application instructions:
- Apply today.
- 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 meetings 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.
- Provide 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/Requirements:
- Bachelor’s degree in biological or engineering science.
- Minimum 5 years relevant experience in biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment.
- Ability to collaborate and communicate cross-functionally.
- Proven attention to detail.
Benefits (as stated): discretionary annual bonus; Medical, Dental, Vision; short-term and long-term disability; company paid basic life insurance; 401k company match; paid time off and paid holiday; wellness and transportation benefits.
Application instructions:
- Apply today.