Cell Therapy Manufacturing Associate I — Start Your Cure

Cellipont; Research Forest (TX); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

401K match

Tuition Reimbursement

Employee Referral Bonuses

Flexible work schedules

Job summary

Cellipont Bioservices is seeking an entry-level Manufacturing Associate I to assist in planning and executing GMP cell manufacturing operations in a state-of-the-art facility. The role emphasizes primary cell isolation and cell culture in aseptic conditions, aligned with regulatory requirements for clinical studies.

The candidate will support facility readiness, data capture for regulatory filings, and cross-functional activities while maintaining a culture of safety, quality, and on-time

Qualifications

• Bachelor’s degree in Life Sciences; GMP experience preferred.
• 0-1+ years in cell manufacturing within a GMP environment.
• Understanding of GMP and GDP requirements.
• Excellent communication and time management; able to train others.

Responsibilities

• Assist operation of GMP cell manufacturing plant in compliance with FDA/ISO and QA.
• Maintain production area and processes in accordance with internal/external standards.
• Support processing functions: lab cleanup, equipment maintenance, inventory handling.
• Ensure safety, quality, accountability, and on-time delivery.
• Identify risks and notify supervisor; support regulatory data capture.
• Escalate equipment needs and perform routine monitoring/troubleshooting.

Skills

Communication skills

Time management

Team training

Problem solving

Education

Bachelor’s degree in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Microsoft Projects

Visio

Job description

Cellipont Bioservices is seeking an entry-level Manufacturing Associate I to assist in planning and executing GMP cell manufacturing operations in a state-of-the-art facility. The role emphasizes primary cell isolation and cell culture in aseptic conditions, aligned with regulatory requirements for clinical studies.

The candidate will support facility readiness, data capture for regulatory filings, and cross-functional activities while maintaining a culture of safety, quality, and on-time