CareerPlan

Supervisor, Manufacturing Mon to Fri 3PM to 11:30 PM

Madison, WI, USAFull-time2026-08-07 → 2026-11-12
Hybrid · United States

Core

Lead a manufacturing team in aseptic and medical device production, ensuring compliance with FDA regulations and safety guidelines while executing production plans across multiple shifts.

Role type

Manufacturing Supervisor (cGMP)

Builds

Aseptic and non-aseptic medical device products

Domain

Biopharma / Medical Devices

Required skills

GMP compliance, FDA regulation knowledge, aseptic manufacturing, team leadership, production planning, risk mitigation, performance management, continuous improvement, deviation/CAPA management, inspection readiness

Preferred skills

3-5 years leading direct reports, cross-functional collaboration

Technologies

cGMP systems, ISO-rated cleanroom environments

Responsibilities

Supervise aseptic and medical device manufacturing team; coordinate manufacturing personnel to meet scheduled work; ensure safety and regulatory compliance; plan and execute manufacturing instructions; manage staff performance and recruitment; optimize processes with enabling groups; establish and report KPIs; lead investigations and CAPAs; ensure inspection readiness; identify continuous improvement opportunities.

Seniority

Mid-level Supervisor, hands-on leadership