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Senior Quality Incoming/Process Supervisor

Grecia, Costa Rica💼 Full-time🗓 2026-07-02 → 2026-07-31

Core

Lead and supervise Quality Control teams for incoming, in-process, and finished product inspections, document review, and validation testing to support manufacturing goals and regulatory compliance.

Role type

Senior Quality Supervisor (Manufacturing)

Builds

Production batches of medical devices or regulated products

Domain

Medical device manufacturing / Regulated manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Quality Management System (QMS) regulations, ISO 13485, MDSAP, nonconformance investigations, corrective action implementation, process improvement, audit support, personnel training and evaluation, cross-functional partnership

Preferred skills

Corrective and preventive actions (CAPA), root cause analysis methodologies

Technologies

ISO 13485, MDSAP

Responsibilities

Lead and supervise Quality Control teams; Manage daily quality operations across shifts; Review and approve quality records and batch documentation; Coordinate product holds and disposition activities; Monitor quality metrics and nonconformance trends; Develop, train, and evaluate Quality Control personnel; Partner with Engineering and Manufacturing functions; Support internal and external audits

Seniority

Senior, hands-on IC

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