Quality Control Associate I

Job Description

Job Description

WHO WE ARE

Parse Biosciences is a global life sciences company whose mission is to accelerate progress in human health and scientific research. Empowering researchers to perform single cell sequencing with unprecedented scale and ease, our pioneering approach has enabled groundbreaking discoveries in cancer treatment, tissue repair, stem cell therapy, kidney and liver disease, brain development, and the immune system.

Founded based on a transformative technology invented at the University of Washington, Parse has raised over $100 million and is used by over 3,000 labs across the world. Our growing portfolio of products includes Evercode Whole Transcriptome, Evercode TCR, BCR, Gene Capture, and a software tool for data analysis.

Parse Biosciences is based in Seattle, Washington's vibrant South Lake Union district, where we recently opened a 34,000 square foot headquarters and state-of-the-art laboratory.

THE POSITION

As a Quality Control (QC) Associate I , you will work as part of the Quality Control team to test and verify that all raw materials and finished goods meet defined specifications for quality, consistency, and performance. In this role, you will test our manufactured products against established standards and release criteria, ensuring our customers receive high-quality, conforming reagents. We are looking for candidates who are highly self-motivated, eager to expand their technical expertise, and committed to their team's success in a fast-paced environment.

IN THIS POSITION, YOU WILL

• Execute Parse's Evercode fixation, whole transcriptome, and immune profiling protocols using established analytical chemistry and genomics techniques such as pipetting, PCR, ELISA, DNA / RNA extraction, bead cleanup, cell counting, quantification, and next-generation sequencing (NGS).
• Follow all established policies, procedures, and practices, including Parse's safety requirements, Parse's Quality System, Good Documentation Practices (GDP), Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), etc.
• Select, receive, and store QC aliquots in order to maintain chain of custody and to help process materials in a safe, compliant, and expeditious manner.
• Identify potential or suspected nonconformities to prevent unintended use or delivery of products, escalating issues to area management.
• Contribute to cross-functional Quality investigations and continuous improvement initiatives. Assist in root cause analyses (RCA) and implementation of proposed corrective and preventive actions (CAPA).
• Assist in writing and revising standard operating procedures, test methods, and batch records consistent with established document management guidelines.
• Participate in the review of test results and disposition of finished goods.
• Perform routine maintenance tasks including cleaning and calibrating equipment, culturing cells, creating inventory requisitions, and organizing inventory and freezers.

FOR THIS POSITION, WE LOOK FOR

JOB CONDITIONS

Parse Biosciences is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, or any other status protected by federal, state, or local law.

As part of our commitment to fairness and inclusion, we do not use artificial intelligence or automated systems to screen job applications. Every application is reviewed by a member of our hiring team to ensure that hiring decisions are made thoughtfully and equitably.

To meet the health and wellness needs of our team, Parse offers a comprehensive benefits package for all full time employees, including :

This is a Non-Exempt / Hourly Position. The range provided reflects the hourly pay range. Market Pay Range - Exact compensation offered will be determined based on the candidate's education, experience, and skills.

$26.44—$34.62 USD