Supervisor, Process Development Engineering
Core
Lead daily media, buffer, and stock solution preparation operations for cell therapy manufacturing, ensuring GMP compliance and operational readiness.
Role type
Supervisor, Process Development Engineering (Cell Therapy Manufacturing)
Builds
Media, buffers, and stock solutions for cell therapy manufacturing
Domain
Biopharmaceuticals / Cell Therapy
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Media and buffer preparation, GMP/GMP-ready operations, aseptic processing, cell culture support, scale-up, laboratory safety, operational leadership, scheduling, troubleshooting, continuous improvement, lean principles
Preferred skills
Cell or gene therapy manufacturing, technology transfer, automation, digital manufacturing systems, Industry 4.0 tools
Responsibilities
Supervise daily media, buffer, and stock solution preparation including scheduling and troubleshooting; Lead, coach, train, and develop team members; Ensure consistent, accurate, and high-quality output following standard work and quality requirements; Plan staffing and resources to meet customer needs; Partner with cross-functional teams to support operational readiness and scalable manufacturing practices; Drive continuous improvement, lean initiatives, and automation solutions; Maintain GMP/GMP-ready compliance, safety, documentation, investigations, CAPAs, and a collaborative team environment
Seniority
Mid-Senior, Hands-on IC with team leadership
