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

Location: Seattle, WA Department: Quality Shift: Monday-Friday, 8am-5pm About Us: this is who we are At Just Evotec Biologic ., 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! The Role: / your challenge, …in our journey 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 Biologic ., 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 forthe execution of day-to-day QA responsibilities for GMP manufacturing, along with building and enhancingthe qualityassurance systems.The role incumbent works both independently and collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance withcGMPsand internal procedures. What You’ll Do: Compile lot release documentation for productdisposition Ensure lot release deliverables are received from key stakeholders prior to Productdisposition Facilitate weekly lot disposition meeting with QA, Manufacturing, QC,etc Review Deviations, OOS, and Change control records to ensure no impacttoProduct 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. Who You Are: Candidate must possess strong focus on right the first time and attention to detail Possess effective task/time management 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 are a must 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 Why Join Us: 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 is a site based role. 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 see them. Are You Still Curious? 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. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision and 401k company match, flexible paid time off and paid holiday, wellness and transportation benefits. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status. #J-18808-Ljbffr Evotec