QA Senior Specialist - Site Based, Redmond, WA - Swing Shifts from 12noon

About the role

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! The Role: / Your challenge, …in our journey We’re looking for a passionate and curious QA Senior 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 Senior 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.

Responsibilities

• Review executed Manufacturing processing Batch Records.
• Lead compliance walkthroughs of Manufacturing and other assigned areas.
• Monitor corrections as appropriate.
• Lead the training of new or junior staff.
• Partner with Manufacturing to ensure compliance in Manufacturing operations.
• Triage Manufacturing events and support event investigations.
• Review and approve Master Batch Records, Process Technical Design, and other related documents.
• Support internal and client audits.
• Present as subject matter expert during audits.
• Execute process performance and product quality monitoring programs.
• Identify potential compliance issues.
• Alert senior management of significant quality, compliance, supply, or 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.

Skills

• Ability to collaborate and communicate cross-functionally.
• Proven attention to detail

Benefits

• Growth Opportunities: continuous learning and development, professional courses, mentorship, new projects.
• Flexible Work Environment: flexible work options to help balance professional and personal life.
• Inclusive Culture: diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
• Innovative Projects: chance to work on groundbreaking initiatives and cutting‑edge technology.
• A Place for Big Ideas: encouragement to think outside the box and share ideas.
• Discretionary annual bonus.
• Comprehensive benefits including Medical, Dental and Vision, short‑term and long‑term disability, company paid basic life insurance, 401k company match.
• Flexible work, generous paid time off and paid holiday.
• Wellness and transportation benefits.

Pay

The base pay range for this position at commencement of employment is expected to be $110,000 to $126,400; base salary offered may vary depending on individual’s skills, experience and competitive market value.

Schedule

Swing Shifts, Wednesday through Saturday, 12:00 PM to 10:00 PM.