Quality Control Specialist

Synthego•Redwood City, CA

32d•Onsite

About The Position

The QC Specialist performs GMP analytical testing with increased independence, contributes to first-pass data review, and supports QC documentation and operational reliability. This role builds on foundational analytical skills and requires consistent execution across multiple method platforms. Available Shift: Shift: Day Hours: 8:00am to 4:30pm Days: Tuesday to Saturday

Requirements

Bachelor’s degree in Biology, Chemistry, Molecular Biology, or related scientific field.
3+ years experience in QC or a regulated analytical laboratory.
Ability to follow detailed SOPs and work with precision and consistency.
Strong attention to detail and adherence to data integrity principles.
Demonstrated proficiency in at least two analytical platforms (HPLC, LC/MS, NGS, etc.).
Working knowledge of GMP, GDP, and general data integrity expectations.

Responsibilities

Execute routine QC assays per approved SOPs (HPLC, LC/MS, UV/Vis, qPCR, endotoxin, NGS, etc.) with minimal supervision.
Prepare and manage samples, reagents, standards, and controls following ALCOA+ principles.
Maintain instrument cleanliness and perform basic assay troubleshooting; escalate instrument or complex issues.
Document all work accurately, contemporaneously, and in compliance with GMP and GDP expectations.
Conduct first-pass data checks for accuracy, completeness, and compliance.
Assist in drafting deviations, nonconformances, or technical summaries with guidance.
Contribute to SOP, worksheet, and test method updates under SME direction.
Support method qualification, execution of method transfer activities, or controlled studies.
Maintain lab organization, equipment readiness, and material inventory.
Mentor junior analysts on routine methods and laboratory best practices.
Perform other duties as assigned.