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

Cyprotex•Redmond, WA

22h•$77,000 - $117,000•Onsite

About The Position

At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated. We’re looking for a passionate and curious Senior QA Specialist, 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 QA Specialist 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. This role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing, along with building and enhancing the quality assurance systems. The role incumbent works both independently and collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. The responsibilities of the employee is based on the assigned QA organization as outlined below.

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.

Responsibilities

Compile release documentation for Product & Raw Material disposition
Ensure release deliverables are received from key stakeholders prior to Product & 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
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.