Quality Supervisor - DHR & Inspection 2nd Shift
Core
Supervise quality inspectors and Final Release (DHR) employees to maintain product inspection standards, ensure regulatory compliance, and support production cells and supplier quality.
Role type
Senior IC Quality Supervisor (Medical Device Manufacturing)
Builds
Production cells, supplier quality support, and quality management systems for medical device manufacturing.
Domain
Medical Device Manufacturing / Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work -> physical/clinical work (Quality Inspection & Release)
Required skills
GxP, GAMP, ISO 13485, non-conformance investigation, process qualification, audit support, team leadership, performance management, root cause analysis, safety compliance
Preferred skills
Bachelor's degree in Life Science/Engineering/Physical Science, prior supervisory experience
Technologies
GxP, GAMP, ISO 13485
Responsibilities
Direct and administer activities of inspectors and DHR employees; evaluate and recommend staffing requirements; 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
Senior, hands-on IC with supervisory responsibilities