CareerPlan

Supervisor, Manufacturing

Bedford, NH, USAFull-time2026-10-28 → 2026-11-10

Core

Lead a manufacturing team in aseptic and medical device production, ensuring compliance with FDA and regulatory standards while managing production plans and staff performance.

Role type

Manufacturing Supervisor (Medical Devices/Biopharma)

Builds

Aseptic and non-aseptic medical device products

Domain

Biopharma / Medical Devices

Required skills

GMP compliance, FDA regulations, team leadership, production planning, safety management, performance management, risk mitigation, continuous improvement, cross-functional collaboration

Preferred skills

3-5 years leading direct reports

Technologies

GMP systems, production scheduling tools

Responsibilities

Supervise aseptic and medical device manufacturing activities; ensure safety and regulatory compliance; coordinate production plans across shifts; coach and develop team members; manage performance evaluations and disciplinary actions; collaborate with cross-functional teams; identify and mitigate operational risks; maintain inspection readiness.

Seniority

Mid-level, hands-on IC with people management