Manufacturing Cell Processing Team Lead

The Team Lead, Cell Processing at Pro Kidney 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.

This is an onsite position based in Winston-Salem, NC. The standard schedule is Sunday through Thursday, 7:00 a.m. to 3:30 p.m. Additional overtime may be required based on business needs. Flexibility to adjust work hours and schedules as needed to support operational priorities is preferred.

• 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.
• Conduct aseptic manufacturing processes in a cleanroom environment, ensuring compliance with sterile techniques and regulatory standards.

• Participate in internal and external audits as required.
• Compile and analyze data, prepare reports, and make recommendations for process improvements.
• Perform routine logbook reviews and data tracking.
• Provide support for process development activities as needed.
• Perform other duties as assigned to support manufacturing operations effectively.

• Education/Training: AS/BS in Biotechnology, Biology, Chemistry, or related field; a Science-related discipline preferred. High School Diploma or equivalent may be considered with significant relevant experience.
• Experience:
  
  Preferred minimum 4-6 years of relevant experience in cell processing, biotechnology manufacturing, or a related field, with 3-4 years of proven expertise in a cGMP-regulated environment.
• Skills/Abilities:
• Thorough knowledge of…