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

About Us

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. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you!

About the Role

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.

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

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

Benefits

• Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
• Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. This role is site-based in Redmond, WA, with visits to our Seattle, WA site.
• Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
• Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
• A Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.
• Comprehensive Benefits: Discretionary annual bonus, medical, dental, and vision coverage, 401k company match, flexible paid time off, paid holidays, wellness, and transportation benefits.

Pay

The base pay range for this position at commencement of employment is expected to be $77,000 to $117,000. Base salary, exempt, offered may vary depending on individual’s skills, experience, and competitive market value.