QA Specialist - Lot Disposition, Site Based, Redmond, WA

QA Specialist (GMP)

What You’ll Do
- Compile lot release documentation for product disposition
- Ensure lot release deliverables are received from key stakeholders prior to product disposition
- Facilitate weekly lot disposition meetings (QA, Manufacturing, QC, etc.)
- Review Deviations, OOS, and Change Control records to ensure no impact to product
- Partner with QA peers to ensure consistency and efficiency
- Alert senior management of significant quality, compliance, supply, and safety risks

Who You Are / Skills
- Strong focus on “right the first time” and attention to detail
- Effective task/time management and organizational skills
- Ability to develop solutions to technical issues of moderate scope
- Ability to organize, analyze/interpret, and communicate individual results
- Motivated self-starter with strong mechanical aptitude
- Strong interpersonal, teamwork, and communication skills

Qualifications
- Bachelor’s degree in biological or engineering science
- Minimum 3 years relevant experience in biopharmaceutical/Pharmaceutical cGMP manufacturing (or similar)
- Ability to collaborate and communicate cross-functionally
- Proven attention to detail

Compensation & Benefits
- Base pay range: $90,000–$100,000 (exempt); may vary with skills/experience/market
- Discretionary annual bonus; Medical, Dental, Vision; 401k match; flexible paid time off and paid holiday; wellness and transportation benefits

Application Instructions
- Take the leap and apply today.