QC Analytical Scientist -Site based, Redmond, WA

Just Evotec Biologics • Redmond, WA

115d • $83,000 - $90,325

About The Position

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! In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a scientist 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. This role provides the QC analysis of raw materials, in-process, drug substance and drug product samples in support of our GMP manufacturing operations at the GMP facilities. These efforts support GMP manufacturing activities for biotherapeutic products.

Requirements

• BS in Chemistry, Biochemistry, or related field.
• 3 years + of Quality Control experience in GMP biopharmaceutical or biotechnology industry.
• Laboratory Experience with either HPLC / UPLC chromatography systems or capillary electrophoresis techniques.
• Familiarity with capillary electrophoresis or chromatography data systems.
• Knowledge of GMP regulations and experience with regulatory compliance inspections.
• Ability to adapt, work in a fast-paced environment, manage multiple projects and priorities at the same time.
• Excellent oral/written and interpersonal communication skills.
• Knowledge of Microsoft Office Suite (Excel, Word, PowerPoint).

Responsibilities

• Dive deep into investigations, method validations and analytical separation methods, always looking for ways to improve and innovate.
• Collaborate with cross-functional teams to explore new possibilities and solutions.
• Bring fresh perspectives to routine testing, qualification, and validations that challenge the status quo.
• Regularly share findings, ideas, and solutions in both team settings and presentations.
• Keep up with the latest trends and developments in biotechnology and pharmaceuticals and use knowledge to inspire and lead.
• Ensure that curiosity-driven questions and exploration lead to measurable, impactful results.
• Perform routine/non-routine QC testing using chromatographic and physiochemical methods.
• Ensure timely and accurate completion of GMP documentation.
• Collaborate with Analytical Development to generate and approve protocols, reports, and other technical documents required for the qualification and transfer of analytical methods.
• Conduct laboratory investigations, deviations, OOS, change controls and CAPAs.
• Support equipment qualification (IQ, OQ, PQ).
• Create, maintain, and revise SOPs, methods and associated documents.
• Support all operations of the QC labs including the ordering supplies and maintaining laboratory equipment and lab spaces.
• Support client audit/inspection readiness plans and interact with regulatory agencies during inspections on analytical related matters.
• Participate in daily and weekly operation meetings.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Warehousing and Storage
• Education Level: Bachelor's degree