
The Team Lead, Cell Processing at ProKidney plays a critical role in leading advanced manufacturing operations, focusing on cell processing, aseptic processing, and ensuring compliance with cGMP guidelines. This role involves overseeing day-to-day operations of the manufacturing team, troubleshooting issues, leading deviation and CAPA investigations, and mentoring staff. The Team Lead is a Subject Matter Expert (SME) in manufacturing processes, driving continuous improvement, ensuring high-quality GMP documentation, and promoting operational efficiency.
Monday through Friday 10am-630pm onsite in Winston Salem, NC
Lead the day-to-day operations of the manufacturing team, ensuring all manufacturing processes are completed efficiently and effectively.
• Initiate manufacturing deviations, Corrective and Preventive Actions (CAPAs), and Critical Change Requests (CCRs) as required, leading investigations and compiling relevant data and information.
• Serve as a Subject Matter Expert (SME) on all manufacturing processes, providing guidance and training to team members.
• Quickly and efficiently troubleshoot manufacturing issues, directing team members on corrective actions.
• Complete manufacturing batch record reviews for all manufacturing processes, ensuring compliance with cGMP guidelines.
• Participate in the aseptic processing of in-house solutions and patient processes in accordance with cGMPs.
• Read, understand, and follow Standard Operating Procedures (SOPs) and assist in the development and revision of SOPs, batch records, and MS forms as needed.
• Assist in the selection, hiring, training, and mentoring of new staff, ensuring personnel are adequately trained and scheduled to support manufacturing operations.
• Perform routine transactions in the ERP system, including material requisitions, production tracking, work order updates, and managing production BOMs.
• Complete GMP documentation, including batch records, logbooks, and forms, according to Good Documentation Practices (GDP).
• Support the maintenance of the cleanroom environment, ensuring cleanliness and compliance with alert-level limits.
• Comply with all relevant safety policies, rules, and regulations, ensuring team members adhere to safety protocols.
• Perform procedures according to written guidelines, recognizing deviations from accepted practices, and taking corrective action as necessary.
• Lead and direct the work of others, with a wide degree of creativity and latitude expected. May provide consultation on projects and serve as a high-level contributor/specialist.
Secondary Responsibilities:
Minimum Qualifications:
ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.
Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.

ProKidney, a pioneer in the treatment of chronic kidney disease through innovations in cellular therapy, was founded in 2015 after a decade of research. ProKidney’s lead product candidate, rilparencel (also known as REACT®), is a first-in-class, patented, proprietary autologous cellular therapy being evaluated in Phase 2 and Phase 3 studies for its potential to preserve kidney function in diabetic patients at high risk of kidney failure. Rilparencel has received Regenerative Medicine Advanced Therapy (RMAT) designation from the FDA. For more information, please visit www.prokidney.com.