Supervisor- Quality Systems (Documentation Center)
Core
Supervise the Document Control Department in Costa Rica to ensure efficient, consistent operation aligned with corporate standards and regulatory requirements, managing controlled documentation for medical products.
Role type
Senior IC Quality Systems Supervisor (Documentation)
Builds
Controlled documentation repositories, change control systems, and audit-ready records for medical products.
Domain
Life Sciences / Medical Devices / Quality Systems
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Supervision and coordination, Change control management, Audit preparation and closure, Process improvement, Budget definition, Cross-functional collaboration
Preferred skills
Master's degree in related field, C1+ English proficiency, ISO 13485 experience, Project management
Technologies
SAP, OneVault, Salesforce, Arena, Windchill
Responsibilities
Supervise and coordinate Document Control Department activities, Assign and follow up on team work for compliance, Ensure custody and traceability of controlled documentation, Coordinate Change Control Board administration, Monitor departmental metrics and identify improvement opportunities, Support coordination for critical documentation and training requests
Seniority
Senior, hands-on IC