Quality Systems Supervisor
Core
Supervise the Document Control Department in Costa Rica to ensure efficient, consistent operation aligned with corporate and regulatory standards for medical products.
Role type
Quality Systems Supervisor (Document Control)
Builds
Controlled documentation, change control systems, and document repositories for medical products.
Domain
Medical devices / Regulated industry / Quality Systems
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Supervision and coordination, compliance with Quality System requirements, change control administration, audit preparation, process improvement, budget management, electronic documentation systems proficiency
Preferred skills
Master's degree in related field, C1+ English proficiency, ISO 13485 experience, project management experience
Technologies
SAP, OneVault, Salesforce, Arena, Windchill
Responsibilities
Supervise and coordinate Document Control Department activities, assign and prioritize team work, ensure custody and traceability of controlled documentation, coordinate Change Control Board administration, monitor departmental metrics, support internal and external audits, define and control budget
Seniority
Mid-level, hands-on supervisor