Cell Processing Associate I
About The Position
RoslinCT is 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. 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.
Requirements
- 0-2 years of experience with Bachelor's degree in biology or related scientific discipline, or equivalent combination of experience and education
- Excellent skills in Microsoft Word, Excel, and commonly used Manufacturing and Quality systems
- Comfortable in a fast-paced and dynamic environment with minimal direction and able to adjust workload based upon changing priorities
- A highly organized work style that ensures timely execution of tasks.
- A mindset that ensures accurate results.
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
- Effective problem-solving capabilities.
- Strong oral and written communication skills.
Responsibilities
- Assist with daily activities of a new cGMP facility by collaborating with Validation, MST, Facilities and Quality departments
- Perform manufacturing processes on the floor, following validation protocols, batch records and standard operating procedures (SOPs) to ensure safe and compliant operations
- 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
- Assist peers with deviations and root cause analysis in the event of any discrepancies that arise during processing
- As part of a team, 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
- Escalate processing and equipment issues as needed
- Daily review of in-process cGMP documentation for completeness and accuracy
- Other duties as assigned by Supervisor or Manager
Benefits
- flexible and empowering work environment
- attractive benefits package
- emphasis on work-life balance
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
