Senior Automation Engineer

Posted 7 Days Ago
Be an Early Applicant
Boston, MA
7+ Years Experience
Biotech
The Role
Seeking a Senior Automation Engineer to develop novel gene editing therapies for serious diseases. Responsibilities include developing and optimizing liquid handler protocols, implementing automated workflows, troubleshooting automation systems, and collaborating with internal and external groups. Minimum qualifications include a B.S. or M.S. in biology/engineering/biotechnology, 6-10+ years of relevant experience, expertise in laboratory automation control software and liquid handling, and strong communication and programming skills.
Summary Generated by Built In

Company Overview

Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Bayer and Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California, and business offices in London, United Kingdom.

Position Summary

We are seeking a Senior Automation Engineer to join an exciting, fast-paced, and well-financed company to develop novel gene editing therapies for serious diseases. The successful candidate will understand molecular biology protocols and techniques, have a mindset for efficiency and troubleshooting, and display a strong interest in laboratory automation. This position requires enthusiasm, attention to detail, and a desire to create new medicines for patients.

Responsibilities

  • Develop and optimize new liquid handler protocols for the screening and high-throughput assay platforms, specifically using Hamilton Venus
  • Work with scientists to develop, optimize and implement automated workflows
  • Perform lab automation operations including protocol design, error recovery, position-teaching, etc
  • Drives software communication drivers between lab automation systems
  • Deploy integrated lab automation solutions based on dynamic scheduling systems
  • Track/record problems with the automated systems and assay setups for proper troubleshooting
  • Explore, evaluate, and implement newer hardware and digital control technologies in automation, to improve on sample analysis
  • Train users on new methods and protocols of system functionalities to automate processes using automated liquid handling and other modular platforms
  • Educate users about lab automation instruments, software and their capabilities
  • Collaborate and coordinate with internal and external groups to identify appropriate solutions to improve capacity and efficiency

Minimum Qualifications

  • B.S. or M.S. in biology/engineering/biotechnology or related field
  • 6-10+ years of relevant experience or 4-8 years with advanced degree
  • Proven experience in developing, validating, and troubleshooting methods and instruments for liquid handling, particularly Hamilton liquid handlers
  • Expertise in VENUS laboratory automation control software
  • Experience with LIMS systems or database
  • Ability to work in a fast-paced multi-tasking environment
  • Must demonstrate an ability to troubleshoot complex problems on automation equipment
  • Prior experience successfully automating manual lab processes
  • Strong communication and programming skills.

Preferred Qualifications

  • Prior research experience in the biotech industry with a focus on next-generation sequencing
  • Prior experience with amplicon sequencing, LNP/mRNA production
  • Expertise in Python, R, Java, or other scripting languages
  • Experience with Benchling workflows

Competencies

  • Collaborative – Openness, One Team
  • Undaunted – Fearless, Can-do attitude
  • Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit – Proactive. Ownership mindset.

Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site.

The Company
HQ: Cambridge, MA
508 Employees
On-site Workplace
Year Founded: 2013

What We Do

CRISPR Therapeutics is a leading gene editing company focused on developing transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. CRISPR/Cas9 is a revolutionary gene editing technology that allows for precise, directed changes to genomic DNA. CRISPR Therapeutics has established a portfolio of therapeutic programs across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine and rare diseases. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic collaborations with leading companies including Bayer, Vertex Pharmaceuticals and ViaCyte, Inc. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Cambridge, Massachusetts, and business offices in San Francisco, California and London, United Kingdom.

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