Quality Supervisor - 2nd Shift/Sign on Bonus
Core
Supervise quality inspectors and final release (DHR) employees to maintain high quality standards, ensure regulatory compliance, and support production cells in a medical device manufacturing environment.
Role type
Mid-level supervisory IC (Quality Supervisor)
Builds
Medical device products and components
Domain
Medical Device Manufacturing / Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work -> physical/clinical work (manufacturing quality control)
Required skills
Team leadership, regulatory compliance (GxP, GAMP, ISO 13485), non-conformance investigation, process improvement, audit support, staff development, operational metrics management
Preferred skills
Bachelor's degree in Life Science/Engineering/Physical Science, previous supervisory experience
Technologies
GxP, GAMP, ISO 13485, Process Excellence tools
Responsibilities
Direct and administer activities of inspectors and DHR employees; evaluate and recommend staffing requirements; create and validate training curriculum; establish measurable goals for team performance; lead inspection strategy for quality projects; support investigations for non-conformances; approve specification and process changes; support internal and external audit programs; promote safety and industrial hygiene objectives; drive continuous improvement in operational metrics.
Seniority
Mid-level Supervisor
