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Inspector de Calidad II – Turno Lunes a Viernes y Sábados

Viant Medical · Heredia

🇪🇸 Español

Job description

About the role

The Quality Inspector II is responsible for inspecting components, assemblies, and finished products to ensure they meet engineering specifications and quality standards. Working under moderate supervision, the inspector supports daily production, shipment verification, and compliance with customer expectations.

Key responsibilities

  • Inspect and test parts, molded and extruded components, sub‑assemblies, and finished goods according to established specifications and test methods.
  • Support the Quality Engineer in resolving non‑conformities, including re‑work, sorting, and re‑inspection.
  • Document results, approve or reject items, and maintain accurate DHR, CoC, and other quality records.
  • Ensure manufacturing processes comply with standard work procedures and correct fabrication practices.
  • Perform in‑process, pre‑sterilization, and post‑sterilization testing; release conforming lots and document non‑conforming batches.
  • Execute ERP (EPR) transactions for final product release, labeling verification, and packaging integrity.
  • Conduct quality audits covering process parameters, calibration expiry dates, preventive maintenance, and line authorizations.
  • Manage quality cages for non‑conforming materials, including segregation and system tracking.
  • Assist in the resolution of complaints and non‑conformities, providing training and root‑cause analysis support.

Required profile

  • Ability to work under moderate supervision while maintaining high attention to detail.
  • Strong documentation discipline and familiarity with quality record‑keeping practices.
  • Understanding of manufacturing processes, sterilization testing, and product release criteria.
  • Effective teamwork skills, collaborating with cross‑functional, QA, and value‑stream teams.

Required skills

  • Proficiency with measurement and testing devices.
  • Experience using ERP/EPR systems for transaction processing.
  • Knowledge of quality documentation (DHR, CoC) and audit procedures.
  • Ability to interpret sterilization test results and apply acceptance criteria.

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Published 1 month ago

Expires 6 days from now

37 views · 0 interested

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Viant Medical

Heredia