Quality Senior Specialist, Raw Material Disposition - Site Based, Redmond and Seattle, WA
Evotec
6 hours ago
On-site
Redmond, WA
Operations
What You’ll Do (GMP Heavy 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.
Who You Are (Qualifications & Competencies) — 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.
Base pay range (salary exempt): $92,400 to $126,500. Additional total rewards include 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 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.
Who You Are (Qualifications & Competencies) — 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.
Base pay range (salary exempt): $92,400 to $126,500. Additional total rewards include 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.