Quality Control Analyst

Synthego

Redwood City, CA Quality
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The QC Analyst performs routine GMP analytical testing and documentation activities that support raw material, in-process, stability, and release testing.

This entry-level role focuses on executing established methods, maintaining accurate and compliant records, and developing technical proficiency across QC operations under close supervision.

Available Shift:


Shift: Swing

Hours: 2:30pm to 11:00pm

Days: Monday to Friday

What You'll Do:

• Execute routine QC assays per approved SOPs (HPLC, LC/MS, UV/Vis, PCR, endotoxin, NGS, etc.).

• Prepare and manage samples, reagents, standards, and controls following ALCOA+ principles.

• Maintain instrument cleanliness and perform routine instrument checks and notify senior staff of any issues.

• Document all work accurately, contemporaneously, and in compliance with GMP and GDP expectations.

• Support routine lab maintenance, inventory, and material readiness.

• Provide test execution details or raw data to support simple deviations or investigations.

• Participate in cross-training to build competency across analytical platforms.

• Perform other duties as assigned.

About You:

• Bachelor’s degree in Biology, Chemistry, Molecular Biology, or related scientific field.

• 1+ 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.

• Relevant combinations of education, experience, certifications, and merit may be considered upon management review.

Perks & Benefits:

• Medical, dental, and vision benefits

• 401k Program

• Catered meals on Tuesday and Thursday

• Paid parental leave

• Flexible paid time off

• Education Reimbursement Program

Our Mission

Synthego® is a pioneering force in the biotechnology industry, dedicated to advancing the frontiers of CRISPR cell and gene therapies through cutting-edge CRISPR technology and expertise. Our mission is to provide unparalleled access to CRISPR solutions at scale, empowering applications from Discovery to Clinic. Driven by a visionary approach, we strive to accelerate the therapeutic development process with best-in-class CRISPR solutions, simplified licensing & expert guidance, driving the adoption and success of CRISPR-based therapies to benefit all patients.

Skills

HPLCLC/MSUV/VisPCRendotoxin testingNGSAttention to detailGMP complianceData integrityAbility to follow SOPs