QC Associate II
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. Onsite Position - 5 Days per week in South San Francisco
Requirements
- Education: BS or MS in Biochemistry, Chemistry, Molecular Biology, or a related scientific field.
- Experience: 2+ years of professional experience in an industrial Operations or QC setting.
- Communication: Excellent verbal and written communication skills with the ability to collaborate across departments.
Nice To Haves
- Quality Standards: Strong working knowledge of QC/QA principles, including GMP and ISO 13485 environments.
- Molecular Biology: Proficiency in techniques such as PCR, Cloning, and NGS.
- Analytical Expertise: Hands-on experience with spectroscopy, gel electrophoresis, and fragment analysis.
- Systems & Automation: Familiarity with automated robotic platforms and Laboratory Information Management Systems (LIMS).
- Problem Solving: A proven track record of troubleshooting and resolving complex technical problems.
Responsibilities
- Product Release: Review and release products based on established QC metrics and rigorous quality standards.
- Data Monitoring: Continuously monitor QC data to identify trends and ensure process stability.
- Issue Resolution: Lead investigations into product, process, and quality issues to identify and mitigate risks.
- Quality Compliance: Review CAPAs and process deviations; perform thorough root cause analysis (RCA) to prevent recurrence.
- Reporting: Prepare comprehensive product and process quality reports by collecting, analyzing, and summarizing key information and performance trends.
- Documentation: Draft and review critical product quality documentation and Standard Operating Procedures (SOPs).
- Regulatory Adherence: Ensure all laboratory activities follow strict regulatory guidelines and ISO 13485 requirements.
Benefits
- In addition to base salary, this role is eligible for bonus, equity, and a generous benefits package.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
501-1,000 employees
