Full-Time

Shipping Associate

Posted on 7/15/2025

Synthego

Synthego

51-200 employees

Supplies synthetic RNA and gene-editing tools.

Compensation Overview

$24 - $26/hr

San Carlos, CA, USA

In Person

Category
Operations & Logistics (1)
Required Skills
Inventory Management
Requirements
  • 2+ years of experience in similar role with increasing responsibilities
  • Proficient with MS Office, GSuite, Smartsheets, and ability to learn new software
  • Able to balance multiple priorities, Pay attention to detail, while maintaining a high level of accuracy
  • Works well under time constraints
  • Thrives in a fast paced environment
  • Team player, able to interact with various functions within the business
  • Strong attention to detail
  • Able to lift 50-75lbs
  • Experience with domestic and international cold chain shipping
Responsibilities
  • Coordinate with operations, quality and commercial operations to ensure daily orders are picked, packed, and shipped on-time
  • Generate domestic and international shipping documents, packing slips, shipping labels, and BOLs documents through DHL/FedEx/ WC automated system or manually, as required to meet Synthego shipping requirements (As per GMP Shipping SOP in case of GMP orders)
  • Properly package and manifest packages and boxes as required to ensure product integrity throughout the transportation cycle to intended destination globally
  • File and maintain records of shipping documents per departmental guidelines
  • Inspect finished product for defects and verify accuracy of order contents and documentation prior to packaging and shipment
  • Ensure all product specified documents necessary for shipment are accurate and accompany shipment in transit
  • Ensure all applicable shipping compliance regulations are upheld
  • Maintain appropriate inventory levels of packaging materials such as boxes, labels, ice bricks, other raw materials and dry ice
  • Maintain a safe workplace in compliance with all company policies
  • Process certified mail and shipping packages for internal customers (HR, legal,FSE, Quality and finance departments) as needed

Synthego provides tools and services for genetic engineering. It sells synthetic RNA and gene editing reagents that researchers use to modify genes, and it offers a platform that gives users access to advanced gene editing workflows. The products are used by research institutions, pharmaceutical companies, and biotech startups for drug discovery, disease modeling, and genetic research. Unlike competitors that only offer individual components, Synthego combines both physical gene-editing tools and an integrated platform to support end-to-end genetic engineering work. The company’s goal is to help researchers perform gene editing more efficiently and at scale, accelerating discoveries in medicine and agriculture.

Company Size

51-200

Company Stage

Series E

Total Funding

$459.7M

Headquarters

Menlo Park, California

Founded

2012

Simplify Jobs

Simplify's Take

What believers are saying

  • Perceptive Advisors acquired Synthego on July 18, 2025, bolstering financial stability.
  • Strategic deals with AstraZeneca and HuidaGene expand nuclease portfolio for therapies.
  • Dr. Bill Skarnes joined advisory board, enhancing stem cell genome engineering expertise.

What critics are saying

  • Perceptive demands cut R&D spending within 6-12 months, eroding innovation edge.
  • EditCo Bio spinout diverts talent and clients from core CRISPR business immediately.
  • IP disputes in AstraZeneca and HuidaGene licenses halt GMP lines in 12-18 months.

What makes Synthego unique

  • Synthego vertically integrates hardware, software, and GMP CRISPR for precise genome engineering.
  • Synthego licenses advanced nucleases like hfCas12Max and eSpOT-ON from AstraZeneca and Vita.
  • Synthego delivers AccuBase base editors via Base Therapeutics and KACTUS partnerships.

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Benefits

Generous Equity Package

Medical, Dental & Vision

401(k) Plan

Catered to You

Fully Stocked

Transportation

Green Environment

Stay Fit

Legal Ease

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

-2%
KACTUS
Oct 28th, 2025
Base Therapeutics and KACTUS Announce Strategic Partnership with Synthego to Advance GMP AccuBase(TM) Base Editing Platform

Base Therapeutics and KACTUS announce strategic partnership with Synthego to advance GMP AccuBase(TM) base editing platform. Home / news & articles / Base Therapeutics and KACTUS announce strategic partnership with Synthego to advance GMP AccuBase(TM) base editing platform. Base Therapeutics and KACTUS are excited to announce a strategic partnership with Synthego for the distribution of the AccuBase(TM) cytosine base editor. This collaboration aims to accelerate innovation and accessibility of next-generation cell and gene therapies. This agreement integrates Base Therapeutics' pioneering base-editing technologies, and KACTUS' leadership in enzyme design and GMP-grade production with Synthego's industry-leading RUO-to-GMP CRISPR Solutions to address unmet needs in the rapidly evolving field of genomic medicine. "We are thrilled to collaborate with Synthego and Base Therapeutics to meet the needs of our global customers and accelerate the availability of therapeutic solutions for disease treatment. Through this alliance, we aim to advance the research and industrialization of cell and gene therapy," said Edmund Wang, CEO of KACTUS. Traditional CRISPR editing systems such as Cas9 or Cas12 rely on DNA double-strand breaks, introducing risks such as chromosomal loss or translocation. In contrast, the AccuBase(TM) cytosine base editor represents "CRISPR 2.0" technology that enables ultra-precise, cell-friendly editing with near-zero off-target effects. As the only GMP-grade base editing proteins currently available, AccuBase(TM) marks a new era for gene editing, shifting from "cutting" to "precision modification". "AccuBase(TM) is the next evolution of our clinical-grade solutions, complementing our best-in-class Guide RNA with a powerful base editing platform. With over five years of proven GMP experience and regulatory guidance, we are uniquely positioned to empower our therapeutic partners and accelerate their path to the clinic," said Craig Christianson, CEO of Synthego. "This partnership represents an important milestone in the global expansion of AccuBase(TM). We look forward to working with therapeutic partners to ensure that gene-editing technologies truly benefit human health worldwide," said Dr. Tianhong Xu, Founder and CEO of Base Therapeutics. As a leading supplier in cell and gene therapy, KACTUS provides an extensive portfolio of gene-editing enzymes - including GMP-grade Cas9 (FDA DMF filed) and GMP-grade AccuBase(TM)- to support customers throughout the IND and clinical phases of drug development. By integrating their respective scientific, commercial and regulatory strengths, this strategic partnership will advance the development of next-generation gene editing technologies, establishing a new standard for safe and effective tools in therapeutic applications. About KACTUS. KACTUS is an innovation-driven company specializing in recombinant proteins and enzyme materials to support the development and manufacturing of biopharmaceuticals. Established in 2018, KACTUS has built deep expertise in protein R&D and production through its proprietary structure-designed protein platform, SAMS(TM). With its own 100,000 square foot GMP facility and certified quality system, KACTUS supplies a broad range of GMP-grade raw proteins and enzymes tailored to the needs of cell and gene therapy drug development. About Synthego. Synthego is a leader in biotechnology, dedicated to delivering best-in-class CRISPR solutions with a mission to accelerate research and development in the pursuit of improved human health. By providing unparalleled access to CRISPR solutions at scale, Synthego enables agility in life science discovery and clinical advancement. With streamlined licensing models and exceptional technical expertise, Synthego empowers researchers and developers to unlock better patient outcomes through innovative CRISPR cell and gene therapies. Recognized in hundreds of peer-reviewed publications and trusted by thousands of researchers and therapeutic developers, Synthego is driving the future of medicine through cutting-edge genome-editing technologies. About Base Therapeutics. Founded in 2021, Base Therapeutics is a high-tech enterprise focused on breakthrough innovations in gene editing. The company holds more than 30 domestic and international patents and is developing first-in-class cell and gene-editing products, particularly in cancer and rare genetic diseases. Its pipeline includes base-editing CAR-T and in vivo base-editing therapies, as well as NK510 and NK520 programs. Base Therapeutics' NK cell base-editing therapies are already in clinical studies exploring efficacy and safety in relapsed, refractory, and metastatic solid and hematologic tumors where conventional chemotherapy has failed.

Pulse 2.0
Jul 22nd, 2025
Synthego Acquired by Perceptive Advisors

Synthego has completed the sale of nearly all its assets to funds managed by Perceptive Advisors, finalized on July 18, 2025. Under Perceptive's ownership, Synthego will continue its operations with the same leadership and brand. The acquisition aims to enhance Synthego's financial position and accelerate innovation in CRISPR solutions. Recent product expansions include a GMP version of SpCas9 and new enzymes, eSpOT-ON and Accubase.

CRISPR Medicine News
Jun 27th, 2025
CMN Weekly (27 June 2025) - Your Weekly CRISPR Medicine News

Perceptive Advisors' acquisition of Synthego, a leader in CRISPR solutions, has been cleared to close in July.

Health Technology Insights
Apr 8th, 2025
Synthego and Vita Therapeutics License hfCas12Max CRISPR

Synthego introduced the hfCas12Max CRISPR system in 2024, the first in its portfolio of high-fidelity nucleases designed specifically for therapeutic applications.

PR Newswire
Apr 8th, 2025
Synthego And Vita Therapeutics Announce Strategic Licensing Agreement For Hfcas12Max Crispr Nuclease

REDWOOD CITY, Calif., April 8, 2025 /PRNewswire/ -- Synthego and Vita Therapeutics, Inc. today announced a licensing agreement to integrate Synthego's high-fidelity hfCas12Max CRISPR system into Vita's cell therapeutic programs. This nonexclusive sublicense grants Vita Therapeutics access to the engineered hfCas12Max nuclease and optimized hfCas12Max guide RNAs for use in preclinical and clinical applications, including in potential commercialized therapeutics. "With the integration of hfCas12Max, Vita Therapeutics can accelerate the development of their hypoimmunogenic cell therapies, paving the way for life-changing treatments to reach patients sooner," said Craig Christianson, CEO of Synthego. "Our goal is to make therapeutic CRISPR solutions more accessible by removing traditional bottlenecks with reduced upfront licensing fees and a lower total IP cost as the therapy advances."

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