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

Location: Seattle, WA | Department: Quality | Shift: Monday-Friday, 8am-5pm

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? #BeCurious with us and see where your curiosity can take you!

About the Role

We’re looking for a passionate and curious 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 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.

Just-Evotec Biologics is seeking a highly motivated QA Specialist that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be 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 lot release documentation for product disposition
• Ensure lot release deliverables are received from key stakeholders prior to Product 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

• Strong focus on "right the first time" and attention to detail
• Effective task/time management and organizational skills
• Capacity to develop solutions to technical issues of moderate scope
• Ability to organize, analyze/interpret, and effectively communicate individual results
• Motivated, self-starter with strong mechanical aptitude
• Good interpersonal, team, and communication skills
• Excellent oral and written communication skills

Qualifications

• Bachelor’s degree in biological or engineering science
• Minimum of 3 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: Professional courses, mentorship, and new projects to support continuous learning and development
• Flexible Work Environment: Site-based role with flexible work options to help balance professional and personal life
• Inclusive Culture: Commitment to building a diverse and inclusive environment where everyone’s voice is valued
• Innovative Projects: Opportunity to work on groundbreaking initiatives and cutting-edge technology
• Discretionary annual bonus
• Comprehensive benefits including Medical, Dental, and Vision
• 401k company match
• Flexible paid time off and paid holidays
• Wellness and transportation benefits

Pay

The base pay range for this position at commencement of employment is expected to be $90,000 to $100,000. Base salary, exempt, offered may vary depending on individual’s skills, experience, and competitive market value.