Unlock innovative solutions in cell therapy manufacturing by leading technology transfers, optimizing processes, and driving compliance in a dynamic, multidisciplinary environment focused on scalability and operational excellence.

The Quality Control Analyst will conduct routine and non-routine QC testing in accordance with Standard Operating Procedures (SOPs) to support the Quality Control group. This role involves analytical testing of in-process materials, raw materials, and finished goods, ensuring compliance with cGMP guidelines.

Contribute to rigorous quality control processes ensuring raw material compliance in a fast-paced, mission-driven environment. Collaborate cross-functionally to execute inspections, testing, and documentation in alignment with cGMP standards.

Lead the charge in ensuring optimal function and compliance of GMP manufacturing equipment. Contribute to a fast-paced environment through hands-on maintenance, troubleshooting, and cross-functional collaboration to drive quality and efficiency.

Accelerate progress at a leading cell therapy manufacturing facility by overseeing cGMP operations. Drive compliance, foster teamwork, and ensure timely product delivery while mentoring staff in a mission-driven, fast-paced environment.