Cell Processing Associate II-- 3rd shift

Cell Processing Associate II-- 3rd shift

This range is provided by Roslin

CT. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$60,000.00/yr - $95,000.00/yr

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Roslin

CT 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 Roslin

CT, 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 Roslin

CT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.

This is a third shift role reporting to the Manufacturing Supervisor. The position's core responsibilities are focused on clinical and commercial manufacturing processes related to cell therapies. Activities include aseptic sampling of products in a Grade A environment, operating automated, single‑use systems for the targeting, expansion, and harvesting. Operate and maintain cell processing equipment. The Cell Processing Associate will support inventory management, suite cleaning, and setup activities per Roslin

CT’s governing procedures. This position may require the individual to collaborate as needed with peers within Manufacturing Sciences and Technology (MS&T), Quality, and Facilities.

• Assist with operations in a state‑of‑the‑art cGMP facility by providing direct support to Manufacturing and GMP support activities to ensure seamless production across shifts.
• Perform hands‑on manufacturing processes on the production floor by executing validated protocols, batch records, and SOPs to ensure safe, compliant operations.
• Carry out daily aseptic sampling to evaluate cell count, viability, and other key process parameters.
• Process clinical material using automated, single‑use systems for cell selection, expansion, harvest, and washing steps.
• Support inventory management, material kitting, and transfers in compliance with established SOPs.
• Execute setup and cleaning activities for equipment and clean rooms per defined schedules in compliance with GMP/GDP standards.
• Participate in engineering and GMP runs in close collaboration with MS&T and other operational teams.
• Adhere to cGMP regulations and SOPs while ensuring accurate and timely completion of all associated documentation.
• Review in‑process documentation daily to verify completeness and compliance with cGMP standards.
• Escalate any processing or equipment issues promptly to ensure timely resolution and minimal impact on production.
• Perform other duties as assigned by the Supervisor or Manager to support operational readiness and execution.

• 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.

• 0–5 years of experience with a Bachelor’s degree in biology or related scientific discipline, or an equivalent combination of experience and education.
• Physical ability to perform routine cleanroom tasks, including gowning and standing for extended periods.
• 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.

All Roslin

CT employees embrace the…