Full-Time

Associate Director

MS&T

Posted on 5/31/2024

Editas Medicine

Editas Medicine

201-500 employees

Develops CRISPR-based gene editing therapies

Biotechnology

Senior, Expert

Cambridge, MA, USA

Requirements
  • Bachelor’s degree in a relevant scientific field
  • 8+ years of experience in pharmaceutical manufacturing, manufacturing science & technology, technical development or Quality
  • 5+ years of experience in executing process validation
  • Expertise with biologics cGMP manufacturing
  • Experience in cell and gene therapy preferred
  • Thorough understanding of industry guidance’s and regulations
  • Experience in leading a team of direct reports
Responsibilities
  • Building and leading a team of engineers, scientists, and associates
  • Leading deviation writing team and owning complex manufacturing investigations
  • Establishing MS&T SOP’s and Tech Transfer Roadmap
  • Leading and initiating guidelines for the CPV program
  • Providing input for Regulatory documents and representing the department during audits
  • Establishing and maintaining the Process Validation Master Plan
  • Creating an environment of learning and information cross-functionally
  • Performing managerial duties pertaining to employees

Editas Medicine is a leader in the biotechnology industry, focused on developing cutting-edge CRISPR gene editing technologies to create transformative medicines for serious diseases. This focus places the company at the forefront of genetic research and therapy development, providing a dynamic and pioneering environment for its employees. As a workplace, it promises a culture of constant learning and innovation, ideal for those passionate about advancing healthcare and contributing to vital medical breakthroughs.

Company Stage

IPO

Total Funding

$884.6M

Headquarters

Cambridge, Massachusetts

Founded

2013

Growth & Insights
Headcount

6 month growth

16%

1 year growth

32%

2 year growth

19%