QA Associate - Site Based, Redmond, WA

Job Title QA Associate Location Redmond, WA (onsite) Shift Details Days, Mon to Fri, 8‑hour shifts ending 16:00, with ad‑hoc days for business requirements. 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! The Role We’re looking for a passionate and curious QA Associate 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. The QA Associate role is responsible for the execution of day‑to‑day QA responsibilities for GMP manufacturing. This role works collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. What You’ll Do Review executed Manufacturing Batch Records. Participate in compliance walkthrough of the Manufacturing floor and other assigned areas. Partner with Manufacturing to ensure compliance in Manufacturing operations. Review and approve Master Batch Records and other supporting documents. Execute process performance and product quality monitoring programs. Alert senior management of potential deviations or compliance risks. Initiate and review all quality events of eQMS (Deviations, Change Control, CAPA, Risk Assessment, Management Review, Complaint Investigation, Product Quality Review etc.) to assure compliance with regulatory and Just‑Evotec Global Quality Management Systems (G‑QMS) requirements. Support QA QMS in internal and external client audits and regulatory inspections (including but not limited to SME for QMS processes and individual records). Monitor effectiveness for QMS through trending, analysis, and metrics; report to top management and G‑QMS on the performance of the KPIs and identify opportunities for continuous improvement. Act as the QA representative on cross‑functional product teams to integrate stability activities with project milestones. Qualifications & Experience Bachelor’s degree in biological sciences, chemistry, biochemistry, engineering, or related life science field. Minimum of 2 years relevant experience in a biopharmaceutical/pharmaceutical cGMP manufacturing or similar environment. Strong attention to detail. Ability to collaborate and communicate cross‑functionally. Benefits Growth opportunities: continuous learning and development. Flexible work environment: flexible work options to help you balance your professional and personal life. This is a site‑based role in Redmond, WA. Inclusive culture: diverse and inclusive environment where everyone’s voice is valued. Innovative projects: work on groundbreaking initiatives and cutting‑edge technology. A place for big ideas. Compensation The base pay range for this salaried non‑exempt position at commencement of employment is expected to be $78,000 to $82,000; base salary offered may vary depending on an individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits (Medical, Dental, Vision), short‑term and long‑term disability, company‑paid basic life insurance, 401(k) company match, flexible work, generous paid time off and holiday, wellness and transportation benefits. EEO Statement 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