Cell Processing Associate

3 weeks ago

Hopkinton, United States RoslinCT Full time
Job DescriptionJob Description

WHO WE ARE 

We at RoslinCT, are a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.

THE ROSLINCT WAY 

Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success, at RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.

ACCELERATING YOUR FUTURE 

Reporting to the Manufacturing Supervisor, this position's core accountabilities are focused on manufacturing processes related to cell therapies. Activities include aseptic sampling of product in a Biosafety Cabinet (BSC) in an ISO V environment, operation of incubators in an ISO VII environment, as well operating automated, single-use systems for the targeting, expansion and harvesting of cells. The Sr. Cell Processing Associate will also collaborate as needed with peers within Manufacturing Sciences and Technology (MST), Quality and Facilities.

 HOW YOU WILL MAKE AN IMPACT 

  • Perform daily aseptic sampling for cell count, viability and other parameters.

  • Perform Equipment and Cleanroom cleaning activities in accordance with established procedures and schedule.

  • Work as part of a team to execute engineering and GMP runs in close collaboration with MST and operations

  • Work as part of a team and lead some deviation and root cause analysis in the event of any discrepancies that arise during processing.

  • Process clinical material in automated systems as part of selection, expansion harvest and wash of cells in single use systems.

  • Adhere to SOPs and cGMP regulations and accurately complete documentation associated with clinical manufacturing.

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