Project Manager
External Manufacturing
Confirmed live in the last 24 hours
Editas Medicine

201-500 employees

Clinical stage genome editing for disease treatment
Company Overview
Editas Medicine stands out as a leader in the field of genomic medicine, leveraging the potential of CRISPR gene editing technology to develop treatments for serious diseases. The company fosters a vibrant culture, encouraging collaboration and resilience among its team of 'Editors', and is committed to manufacturing and commercializing durable, precision genomic medicines. With a robust pipeline of treatments in development, Editas Medicine is not only repairing broken genes but also shaping the future of medicine.
Biotechnology

Company Stage

N/A

Total Funding

$884.6M

Founded

2013

Headquarters

Cambridge, Massachusetts

Growth & Insights
Headcount

6 month growth

8%

1 year growth

9%

2 year growth

9%
Locations
Cambridge, MA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Management
Customer Service
CategoriesNew
Business & Strategy
Customer Success & Support
Requirements
  • Strong project management experience and proven track-record of managing external project to completion
  • Exceptional organizational skills with the ability to multi-task and prioritize assignments
  • Self-motivated with ability to work under pressure to meet deadlines
  • Strong team player that has a customer service approach and is solution oriented
  • Attention to detail and the ability to work individually, within a multi-disciplinary team in a matrix environment, as well as with external partners and vendors
  • B.S. in engineering, life sciences or related field with 5+ years of experience in biotech/pharmaceutical industry with experience working with external partners and vendors and at least 3 years of experience in a project management role
Responsibilities
  • Partner with External Manufacturing and CMC to develop and distribute timelines, agendas, meeting minutes, action items, dashboards, decision logs, etc.
  • Create, socialize and manage project plans and timelines with clearly defined goals
  • Run internal and externally facing meetings
  • Identify and escalate timeline risks, mitigations and/or contingency plans
  • Support management of strategic external relationships by aligning internal and external resources to achieve timelines and milestones
Desired Qualifications
  • Experience in CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing
  • Experience in the biotech/pharmaceutical industry
  • Experience in a project management role