QC Scientist Sample Management - Site Based, Remond, WA
About The Position
We’re looking for a passionate and curious QC Scientist 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 QC Scientist at Just E votec 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. Position This role provides process support for the movement and control of QC samples and materials, including in-process, drug substance/product, characterization, retain, and stability samples processed through the QC laboratories at the Seattle and Redmond, WA GMP facilities. with s. This includes, but is not limited to, a focus on LIMS support, stability management, and compliance projects. These efforts support GMP manufacturing activities for biotherapeutic products.
Requirements
- BS in Chemistry, Biochemistry, or related field and with 3-5 years of Quality Control experience in GMP biopharmaceutical or biotechnology industry .
- Experience with LIMS process flow
- 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; and a knowledge of Microsoft Office Suite (Excel, Word, PowerPoint).
Responsibilities
- Ensure timely and accurate completion of GMP documentation.
- Collaborate with the QC team to generate and approve protocols, reports, and other technical documents required for stability methods.
- Collaborate with external vendors fto manange outsourced laboratory testing
- 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
- 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.
- 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 hear them.
- discretionary annual bonus
- comprehensive benefits to include Medical, Dental and Vision
- short-term and long-term disability
- company paid basic life insurance
- 401k company match
- generous paid time off and paid holiday
- wellness and transportation benefits
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
