Manufacturing Associate - 2428

What if you could repair broken genes? That is the question we ask ourselves at Editas Medicine. We’re focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cpf1 (also known as Cas12a) genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for many diseases. We’re looking for talented, dedicated, passionate people to join our team and help us pioneer this field and do big, bold things that have never been achieved before. Are you full of hope, possibilities, and a belief that, working together, we can truly revolutionize the development of medicines to help patients around the world? If the answer is yes, then Editas Medicine is the place for you.

Key Responsibilities & Accountabilities:

• Perform duties as dictated by standard operating procedures (SOPs) for cellular product manufacturing and under GxP guidelines as directed.
• Work in a clean room environment while fully gowned following GMP guidelines and using aseptic technique.
• Work in a Biological Safety Cabinet for open processing operations.
• Operate instrumentation needed for cell manufacturing.
• Accurately complete batch record documentation, all appropriate equipment log entries, and GMP documentation.
• Maintain orderly lab space.
• Maintain sufficient inventory of supplies and reagents for performance of duties. Clean and maintain laboratory equipment in good working order.
• Prepare solutions and culture media as appropriate.
• Work in compliance with all appropriate laboratory regulatory and safety requirements.

Requirements

Knowledge, Skills & Capabilities:

• Preferred experience with primary cell culture, preferably with human cells
• Preferred experience working in a GMP environment
• Self-motivated and detailed-oriented. Willing to be trained to new techniques
• Ability to read and understand Standard Operating Procedures
• Attention to detail
• Good communication skills and the ability to work independently, as well as part of a team
• Preferred experience with GMP document creation/revision
• Preferred experience with Excel and Microsoft Office application

Education & Relevant Work Experience:

•  BS in Biology-related field of study with minimum 1 - 2 years of experience in a GMP environment

Physical & Travel Requirements (if applicable):

• Must be willing and able to travel between Cambridge, Waltham (training only) and Devens locations

Benefits

Benefits Summary:

Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.