Analysis Skills, Artificial Intelligence (AI), Assays, Best Practices, Biology, Chemistry, Data Quality, Detail Oriented, GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), Identify Issues, Laboratory Equipment, Laboratory Techniques, Licensing, Liquid Chromatography-Mass Spectrometry (LC-MS), Mentoring, Molecular Biology, Quality Assurance Methodology, Quality Control, Real-time PCR (qPCR), Reimbursement, Standard Operating Procedures (SOP), Support Documentation, Testing, UV/VIS (Ultraviolet-Visible Spectroscopy)
Quality Control Specialist
Redwood City, CA
Operations Quality /
Full-time /
On-site
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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
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:
- Bachelors 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
$35 - $37 an hour
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.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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