Synthego®
biotechnology
QualityControlSpecialist
Neural analysis suggests this role is
optimal for Mid candidates.
“Quality Control Specialist at Synthego®. Skills: QC assays, HPLC, LC/MS, NGS, GMP, GDP. 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.”
What You'll Achieve.
provide unparalleled access to CRISPR solutions at scale, empowering applications from Discovery to Clinic; 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
Industry & Context.
perform basic assay troubleshoot
What They're Looking For.
Must Have
3+ years experience in QC or a regulated analytical laboratory, Ability to follow detailed SOPs and work with precision and consistency, 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
What You'll Do.
Execute routine QC assays per approved SOPs (HPLC
etc. ) with minimal supervision.
Prepare and manage samples
and controls following ALCOA+ principles.
Maintain instrument cleanliness and perform basic assay troubleshoot.
Document all work accurately
and in compliance with GMP and GDP expectations.
Conduct first-pass data checks for accuracy
Assist in drafting deviations
or technical summaries with guidance.
and test method updates under SME direction.
Support method qualification
execution of method transfer activities
or controlled studies.
Maintain lab organization
and material inventory.
Mentor junior analysts on routine methods and laboratory best practices.
How You'll Work.
Team & Collaboration
Mentor junior analysts on routine methods and laboratory best practices.
Full Job Description
## Available Shift Shift: Day Hours: 8:00am to 4:30pm Days: Tuesday to Saturday ## What You'll Do 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. ## About You 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. 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 ## Additional Information 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 tec
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