Quality Control Analyst

Posted 8 Days Ago
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Redwood City, CA, USA
In-Office
Entry level
Biotech
The Role
The QC Analyst performs GMP analytical testing and documentation, focusing on executing methods and maintaining records under supervision.
Summary Generated by Built In
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 Required

  • Bachelor's degree in Biology, Chemistry or related field
  • 1+ years experience in QC or regulated analytical laboratory
  • Ability to follow detailed SOPs and work with precision
  • Strong attention to detail and adherence to data integrity
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The Company
HQ: Menlo Park, CA
443 Employees
Year Founded: 2012

What We Do

Synthego is a genome engineering company enabling the acceleration of life science research and development in the pursuit of improved human health. The company leverages machine learning, automation, and gene editing to build platforms for science at scale. By vertically integrating hardware, software, bioinformatics, chemistry, and molecular biology, Synthego is at the forefront of innovation advancing the next generation of medicines through providing access to genome editing at an unprecedented scale. //// Our Culture of Diversity: Different Faces from Different Places At Synthego, our differences make us unique, help us innovate, and allow us to persevere. We stand firmly behind our values, strive to achieve representation, and celebrate diversity in perspectives and backgrounds. We welcome all team members to be their best selves as we move forward towards fulfilling our shared vision of revolutionizing genome engineering technology to help make biological therapies accessible to all patients.

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