Quality Control Analyst chez Synthego

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. 

Shift: Swing

Hours: 2:30pm to 11:00pm 

Days: Monday to Friday 

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. 

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. 

Medical, dental, and vision benefits 

401k Program 

Catered meals on Tuesday and Thursday 

Paid parental leave 

Flexible paid time off 

Education Reimbursement Program

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.