QA Associate - Quality Assurance - Site Based, Swing Shifts - Starting 12noon.

About 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. As a QA Associate 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.

Responsibilities

• 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.

Requirements

• 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: 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, Redmond, WA.
• 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.

Pay

The base pay range for this non-exempt position at commencement of employment is expected to be $78,000-$82,000. Base salary offered may vary depending on individual's skills,