Cell Therapy Specialist

Cell Therapy Specialist at Infotree Global Solutions Cell Therapy Specialist at Infotree Global Solutions in Frederick, Maryland Posted in 2 days ago.

Type:

full-time

Job Description:

Must have local to

Maryland Job Description:

We are looking for a Cell Therapy Specialist to join our cutting-edge manufacturing team and contribute to the production of innovative cellular therapies in a highly controlled, GMP-compliant environment. The Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance.

What You'll Do:

As a Cell Therapy Specialist, you will play a critical role in the end-to-end manufacturing of cell-based therapies. Working in a collaborative and highly regulated setting, you will: Execute manufacturing activities in accordance with approved batch records and standard operating procedures Operate and maintain advanced cell processing and bioproduction equipment in classified cleanroom environments Perform routine monitoring, preparation, and cleaning of equipment to ensure operational readiness Identify, troubleshoot, and escalate process or equipment issues in a timely manner Support deviation investigations, root cause analysis, and implementation of corrective actions Contribute to continuous improvement initiatives to enhance quality, efficiency, and compliance Assist in drafting and updating SOPs, ensuring clarity and adherence to regulatory standards Collaborate cross-functionally with Quality, Supply Chain, and other internal teams during manufacturing campaigns Maintain accurate documentation in line with cGMP and data integrity requirements

What We're Looking For:

Bachelor's degree in Life Sciences (Biotechnology, Biology, or related field) OR Associate's degree with at least 1 year of relevant biotech or pharmaceutical manufacturing experience OR High school diploma with 2+ years of experience in a cGMP-regulated environment

Key Skills & Attributes:

Strong understanding of cGMP principles and aseptic manufacturing practices Experience working in cleanroom environments (Grade B/C preferred) Ability to follow detailed procedures with a high level of accuracy Problem-solving mindset with strong attention to detail Effective communication and teamwork skills Willingness to work flexible shifts as needed