Cell Processing Associate (3rd shift)

RoslinCT; Hopkinton (MA); On-site; USD 50,000 - 90,000; Full time

Job summary

Join a world-leading organization in cell and gene therapy, where your contributions will help develop revolutionary treatments. This role involves supporting clinical and commercial manufacturing processes, ensuring compliance with cGMP regulations, and collaborating with various teams. You'll work in a state-of-the-art facility, executing validated protocols and maintaining high standards of quality. If you're passionate about making a difference in patients' lives and thrive in a dynamic environment, this opportunity is perfect for you. Experience a culture that values personal growth, innovation, and teamwork.

Qualifications

• 0-5 years of experience in a scientific discipline.
• Proficiency in Microsoft Office and manufacturing systems.

Responsibilities

• Assist with operations in a cGMP facility ensuring seamless production.
• Perform hands-on manufacturing processes and adhere to SOPs.

Skills

Organizational Skills

Problem-Solving Skills

Communication Skills

Attention to Detail

Education

Bachelor's degree in Biology

Equivalent combination of experience and education

Tools

Microsoft Office Suite

Job description

Direct message the job poster from RoslinCT

Senior Talent Acquisition Manager at Taylor Strategy Partners a Syneos Health Company

WHO WE ARE

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.

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

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 targeting, expansion, and harvesting, and maintaining cell processing equipment. The Cell Processing Associate will support inventory management, suite cleaning, and setup activities per RoslinCT’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.

How You Will Make an Impact:

1. 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.
2. Perform hands-on manufacturing processes on the production floor by executing validated protocols, batch records, and SOPs to ensure safe, compliant operations.
3. Carry out daily aseptic sampling to evaluate cell count, viability, and other key process parameters.
4. Process clinical material using automated, single-use systems for cell selection, expansion, harvest, and washing steps.
5. Support inventory management, material kitting, and transfers in compliance with established SOPs.
6. Execute setup and cleaning activities for equipment and cleanrooms per defined schedules in compliance with GMP/GDP standards.
7. Participate in engineering and GMP runs in close collaboration with MS&T and other operational teams.
8. Adhere to cGMP regulations and SOPs while ensuring accurate and timely completion of all associated documentation.
9. Review in-process documentation daily to verify completeness and compliance with cGMP standards.
10. Escalate any processing or equipment issues promptly to ensure timely resolution and minimal impact on production.
11. Perform other duties as assigned by the Supervisor or Manager to support operational readiness and execution.

What You Will Bring:

1. A highly organized work style that ensures timely execution of tasks.
2. A mindset that ensures accurate results.
3. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
4. Effective problem-solving capabilities.
5. Strong oral and written communication skills.

Qualifications:

1. 0-5 years of experience with a Bachelor's degree in biology or related scientific discipline, or an equivalent combination of experience and education.
2. Physical ability to perform routine cleanroom tasks, including gowning and standing for extended periods.
3. Excellent skills in Microsoft Word, Excel, and commonly used Manufacturing and Quality systems.
4. Comfortable in a fast-paced and dynamic environment with minimal direction and able to adjust workload based upon changing priorities.

OUR COMMITMENT

All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.

RoslinCT is proud to be an equal-opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Science and Manufacturing