Supervisor, Manufacturing Operations 3rd shift (3A)
Core
Lead and supervise daily cGMP manufacturing operations, including equipment setup, assembly, operation, disassembly, and cleaning, ensuring compliant and efficient execution of production plans.
Role type
Manufacturing Operations Supervisor (3rd shift)
Builds
Drug product batches in a cGMP-compliant facility
Domain
Biotechnology / Pharmaceutical manufacturing (cell therapy/aseptic)
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
cGMP compliance, batch record execution and review, shift personnel supervision, SOP adherence, cross-functional team interface, facility audit readiness, technical leadership, team coaching
Preferred skills
cell therapy experience, aseptic manufacturing experience, POMS MES experience, prior supervisory experience
Technologies
POMS MES
Responsibilities
Assign work to shift personnel based on production schedules, execute and witness batch record instructions, monitor GMP compliance, maintain audit-ready facility state, lead Tier 0 and Tier 1 meetings, request and manage MBRs with QA Document Control
Seniority
Mid-level Supervisor, hands-on IC