Supervisor – Finished Drug Product Production
Core
Provide day-to-day operational oversight of radio Finished Drug Product production activities, ensuring compliance with GMP and NRC regulations.
Role type
Supervisor, Finished Drug Product Production
Builds
Radiopharmaceutical therapies for oncology patients
Domain
Biotechnology / Oncology / Radiopharmaceuticals
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP compliance, NRC regulations, batch record execution, equipment setup, line clearance, material preparation, scheduling, validation activities, cross-functional collaboration, KPI compilation, quality event investigation, inventory management, SOP authoring
Preferred skills
Radiation safety best practices, process optimization, troubleshooting, continuous improvement
Technologies
GMP, NRC, EHS, Radiation Safety programs
Responsibilities
Provide day-to-day operational oversight of radio Finished Drug Product production activities; Serve as a functional lead for production operators; Support onboarding and training efforts for production staff; Support and execute validation activities; Collaborate with cross-functional partners to identify opportunities for process optimization; Assist management with operational KPIs and quality event resolution; Support inventory management activities; Promote safety, quality, and compliance culture; Author, review, and revise production technical documentation
Seniority
Supervisor, hands-on IC