Senior Manager, QA Disposition, Site Based, Redmond, WA

Cyprotex • Redmond, WA

3d • Onsite

About The Position

We’re looking for a passionate and curious Senior Manager, QA to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a Senior Manager, QA at Just Evotec Biologics , you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.

Requirements

• Bachelor’s degree in a biological or engineering discipline with 8+ years of relevant industry experience.
• Minimum of 3 years of people management experience.
• Demonstrated experience building and sustaining Quality infrastructure in a growing organization.
• Strong critical thinking skills with deep understanding of biologics regulatory requirements, risk management principles, and science‑based decision making.
• Expertise in Quality Assurance tools, concepts, and methodologies.
• Proficiency with Microsoft Office and electronic quality systems (eQMS), including CMMS, and SAP.
• Strong competencies in communication (written and verbal), attention to detail, data management and analysis, sound judgment, decision‑making, and team leadership.

Responsibilities

• Product and Material Disposition Lead the QA Disposition group to ensure compliant and efficient disposition of materials and products.
• Perform QA disposition of Cell Banks and DS batches manufactured at Just‑Evotec Biologics.
• Perform QA disposition of Cell Banks and DP batches manufactured at contracted CMOs.
• Execute raw material disposition to support manufacturing schedules and supply continuity.
• Manage QA communication and disposition workflows with CDMO client partners.
• Logistics and Material Movement Oversee DS/DP shipments to CMOs for fill/finish operations.
• Support shipment of DS/DP vials for labeling, stability studies, or other testing needs.
• Quality System Oversight Support internal and client audits of the Quality Management System.
• Implement and maintain process performance and product quality monitoring programs.
• Guide team members and cross‑functional partners through the development and maturation of Quality Assurance programs.
• Implement phase‑appropriate quality programs that balance scientific flexibility with compliance expectations.
• Identify, escalate, and communicate significant quality, compliance, supply, or safety risks to senior leadership.
• Identify and escalate compliance risks within the disposition function.
• Participate in the strategic development and continuous improvement of Quality Systems.
• Compile, analyze, and report team KPIs; lead process improvement initiatives within the disposition area.

Benefits

• Growth Opportunities
• Flexible Work Environment
• Inclusive Culture
• Innovative Projects
• A Place for Big Ideas
• discretionary annual bonus
• comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, generous paid time off and paid holiday, wellness and transportation benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 1-10 employees