Quality Supervisor
Core
Supervise quality operations and engineering teams to maintain high manufacturing standards, ensure regulatory compliance, and drive continuous improvement in a complex site environment.
Role type
Senior IC Quality Supervisor
Builds
Quality management systems, compliance documentation, and operational processes 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 (manufacturing quality)
Required skills
Team leadership, regulatory compliance (GxP, ISO 13485), root cause analysis, process improvement methodologies, audit management, staff performance evaluation, safety and industrial hygiene oversight
Preferred skills
Bachelor's degree in Life Science/Engineering/Physical Science, prior supervisory experience, knowledge of GAMP
Technologies
5S, process mapping, visual factory, GxP, GAMP, ISO 13485
Responsibilities
Direct and administer activities of Quality Engineers, Technicians, and Validation Engineers; lead quality projects for new product implementation; support investigations for non-conformances and drive CAPA; ensure compliance with internal and external audit programs; promote problem-solving methodologies to address defects; manage team performance goals and development; ensure safety and industrial hygiene objectives are met.
Seniority
Senior, hands-on IC with supervisory responsibilities