CareerPlan

QMS Manager

Cambridge (US), Massachusetts, United StatesFull-time$102k2026-10-01 → 2026-11-10
Hybrid · United StatesNo visa sponsorship

Core

Supervise QMS team operations, ensure compliance with quality policies and regulations, and manage risk mitigation for product quality.

Role type

Senior QMS Manager (Medical Devices)

Builds

Compliant quality management processes and audit-ready documentation for medical device products

Domain

Medical Devices / Quality Engineering

Required skills

QMS management, regulatory compliance, internal audits, CAPA, root cause analysis, risk assessment, document control, performance management, data analysis

Preferred skills

Medical device regulations, QMS remediation, hosting quality audits, preventive measures

Responsibilities

Supervise day-to-day QMS team operations, manage deployment and maintenance of QMS processes, monitor and report on process effectiveness, prepare for external audits and inspections, conduct risk assessments and manage mitigation activities

Seniority

Senior, hands-on IC with mentorship responsibilities