QC Associate II

Twist Bioscience•South San Francisco, CA

5d•$25 - $36•Onsite

About The Position

The QC Associate II is responsible for the implementation and continuous improvement of Quality Control methods within the production laboratory. Working closely with the Operations team, you will monitor the quality of Twist DNA products using quantitative measurements, fragment analysis, and Next-Generation Sequencing (NGS). The successful candidate will demonstrate a proven ability to make data-driven decisions in a high-throughput environment. Your primary mission is to ensure that all products—from processing and packaging to storage and distribution—comply with Regulatory, Customer, and Twist internal standards.

Requirements

BS or MS in Biochemistry, Chemistry, Molecular Biology, or a related scientific field.
2+ years of professional experience in an industrial Operations or QC setting.
Excellent verbal and written communication skills with the ability to collaborate across departments.

Nice To Haves

Strong working knowledge of QC/QA principles, including GMP and ISO 13485 environments.
Proficiency in techniques such as PCR, Cloning, and NGS.
Hands-on experience with spectroscopy, gel electrophoresis, and fragment analysis.
Familiarity with automated robotic platforms and Laboratory Information Management Systems (LIMS).
A proven track record of troubleshooting and resolving complex technical problems.

Responsibilities

Review and release products based on established QC metrics and rigorous quality standards.
Continuously monitor QC data to identify trends and ensure process stability.
Lead investigations into product, process, and quality issues to identify and mitigate risks.
Review CAPAs and process deviations; perform thorough root cause analysis (RCA) to prevent recurrence.
Prepare comprehensive product and process quality reports by collecting, analyzing, and summarizing key information and performance trends.
Draft and review critical product quality documentation and Standard Operating Procedures (SOPs).
Ensure all laboratory activities follow strict regulatory guidelines and ISO 13485 requirements.