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Full-Time

Laboratory Associate

Clinical Operations

Posted on 10/19/2023

Synthego

Synthego

201-500 employees

Provides synthetic RNA and gene editing tools

Biotechnology

Junior, Mid

San Carlos, CA, USA

Required Skills
Communications
Requirements
  • AA in Chemistry, Biotech Certification, or relevant work experience
  • 1-3 years of industry experience within the manufacturing/production environment
  • Experience working in a highly regulated environment
  • Great communication skills and able to work with various personalities
  • Strong desire to work in a fast-paced, collaborative startup environment
  • Demonstrates strong interpersonal skills, as well as a strong commitment to quality
  • Demonstrates ability to work independently and as part of a team, to meet departmental goals
  • Must be able to lift/move up to 25 pounds
  • Must be able to sit and/or stand for extended periods up to four (4) hours at a time
Responsibilities
  • Synthesize RUO and Clinical grade oligonucleotides by following established SOP's
  • Practice continuous improvement by contributing ideas and suggestions to new and existing processes
  • Operate complex robotic systems to manage liquid product through a highly automated workflow
  • Execute batch production records or protocols independently, efficiently, and in compliance with site and quality management system requirements
  • Handle chemical solutions
  • Print labels for bottles, vials, and boxes
  • Package, seal, inventory, and ship products
  • Ensure laboratory products and supplies are maintained and stocked
  • Capture production data in compliance with site and quality management system requirements
  • Collaborate with Supply chain, Quality Assurance, Warehouse, and other cross-functional teams to meet deadlines

Synthego specializes in biotechnology, focusing on genetic engineering by providing synthetic RNA and gene editing tools. Their products enable scientists to modify genes, which can lead to advancements in disease treatment and agricultural improvements. Synthego serves a variety of clients, including research institutions, pharmaceutical companies, and biotech startups, who utilize their products for drug discovery, disease modeling, and genetic research. The company stands out in the growing genetic engineering market by offering a platform that grants users access to advanced gene editing capabilities, alongside their synthetic RNA products. Synthego's goal is to support and enhance genetic research and applications through their tools and services.

Company Stage

Series E

Total Funding

$459.7M

Headquarters

Menlo Park, California

Founded

2012

Growth & Insights
Headcount

6 month growth

-10%

1 year growth

-37%

2 year growth

-56%
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Simplify's Take

What believers are saying

  • Synthego's licensing agreement with HuidaGene for the hfCas12Max nuclease positions it at the forefront of CRISPR-based therapeutic applications.
  • The addition of Dr. Bill Skarnes to the advisory board and the launch of high-throughput induced pluripotent stem cell genome engineering highlight Synthego's commitment to innovation and expertise.
  • The opening of a new GMP synthesis facility and the launch of IND-enabling gRNAs bolster Synthego's support for the entire discovery-to-clinic continuum, enhancing its market position.

What critics are saying

  • The rapid pace of innovation in the genetic engineering field requires Synthego to continuously advance its technologies to stay competitive.
  • Leadership changes, such as the recent CEO transition, could lead to strategic shifts and potential instability within the company.

What makes Synthego unique

  • Synthego's focus on synthetic RNA and advanced gene editing tools, such as the high-fidelity Cas12 CRISPR nuclease, sets it apart from competitors who may not offer such specialized products.
  • The company's strategic partnerships, like those with HuidaGene and bit.bio, enhance its capabilities in developing next-generation CRISPR-based therapies and synthetic circuitry in cells.
  • Synthego's state-of-the-art GMP manufacturing facility ensures high-quality production of CRISPR components, providing a competitive edge in the clinical development of gene editing therapies.

Benefits

Generous Equity Package

Medical, Dental & Vision

401(k) Plan

Catered to You

Fully Stocked

Transportation

Green Environment

Stay Fit

Legal Ease

INACTIVE